EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

57th Annual ESPE Meeting 2018

 

27 - 29 September 2018 Athens
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  1-RFC14 Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer Flora Bacopoulou Received Received
  1-P1 Evaluation of long term metabolic effects after prenatal dexamethasone treatment in the context of CAH - the Swedish cohort. Lena Wallensteen Received Received
  1-RFC11 DIAGNOSIS AND MANAGEMENT OF PSEUDOHYPOPARATHYROIDISM AND RELATED DISORDERS: FIRST INTERNATIONAL CONSENSUS STATEMENT Susanne Thiele-Schmitz Received Received
  1-RFC10 Patients with GH Insensitivity and IGF-1 Resistance Harbour Copy Number Variants Causing a Silver-Russell-Like Phenotype Emily Cottrell Received Received
  1-RFC6 Allelic variation in key fitness genes is linked with increased severity of obesity in overweight/obese youth Christoph Saner Received Received
  1-RFC2 High-resolution MRI Imaging Of Bone-Muscle-Fat In Glucocorticoid Treated Boys With Duchenne Muscular Dystrophy: Results from the ScOT-DMD study Shuko Joseph Received Received
  1-RFC12 Use of acid-suppressivemedications during infancy and early childhood and its association with type 1 diabetes Sruthi Menon Received Received
  1-RFC5 SERUM LEVELS OF THE SOLUBLE RECEPTOR FOR ADVANCED GLYCATION END PRODUCTSARE REDUCED IN CHILDREN WITH HASHIMOTOS THYROIDITIS Tommaso Aversa Received Received
  1-RFC7 Next generation sequencing results in 142 patients with congenital hyperinsulinism Diliara Gubaeva Received Received
  1-RFC1 The relative contributions of genetic and environmental factors on cortisol metabolism at pre-, mid- and post-pubertal ages. Britt van Keulen Received Received
  1-P2 Contribution of direct measurements of steroids by Liquid chromatography tandem mass spectrometry (LC-MS/MS) in non-classical adrenal hyperplasia (NCCAH) Muriel HOUANG Received Received
  1-RFC8 Male fertility genes located in Y-chromosomal regions display differential mRNA profiles in response to GnRH treatment of cryptorchidism-dependent infertility Faruk Hadziselimovic Received Received
  1-RFC4 Metabolomic changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment Jesús Argente Received Received
  2-RFC11 NATIONWIDE HYPOPHOSPHATEMIC RICKETS STUDY SIKLAR ZEYNEP Received Received
  2-P1 Obesity and cardio-metabolic risk factors among Children and Adolescents with Non Classic 21-Hydroxylase Deficiency Liat de Vries Received Received
  2-RFC8 High Mobility Group Box 1 (HMGB1) is increased in adolescents with Polycystic Ovarian Syndrome (PCOS) and decreases after treatment with myo-inositol in combination with a-lipoic acid (MYOALA) FRANCESCA CIRILLO Received Received
  2-P3 An extremely rare cause of Cushing Syndrome in chidhood Amith Ramcharan Received Received
  2-RFC14 BRITISH SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY AND DIABETESPEER REVIEW OF SPECIALISED PAEDIATRIC ENDOCRINOLOGY SERVICES IN THE UK - EVALUATION OF THE OUTCOMES John Schulga Received Received
  2-RFC2 S-25OHD is Associated with Hand Grip Strength and Myopathy at Five Years in Girls: An Odense Child Cohort Study. Rada Faris Al-Jwadi Received Received
  2-LB Effects on growth, body composition and gross motor and cognitive development and safety of recombinant human growth hormone in infants or toddlers with Prader-Willi syndrome: A randomized, active-comparator controlled Trial Ji-Eun Lee Received Received
  2-RFC15 Molecular and clinical analyses of two UPD(16)mat patients detected by screening of 94 Silver-Russell syndrome patients without known etiology Takanobu Inoue Received Received
  2-RFC6 IGF-I at 4 months associates to visceral and subcutaneous adipose tissue at 7 years of age Emma Kjellberg Received Received
  2-RFC10 Non-inferiority clinical trial on gonadotropinversus pulsatile gonadotropin-releasing hormone infusion therapy in male adolescent patient withcongenital hypogonadotropic hypogonadism Liu Ying Received Received
  2-RFC13 Growth outcomes and near adult height of children with congenital GH deficiency (GHD) due to abnormal pituitary development: data from a prospective, multinational observational study Christopher Child Received Received
  2-RFC3 Personalized and predictive medicine for pediatric diabetes through a genetic test using next generation sequencing Valerie Schwitzgebel Received Received
  2-RFC5 Analysis of chosen polymorphisms rs7138803 A/G - FAIM2, rs7093069 C/T - IL-2RA, rs5742909 C/T - CTLA-4 in pathogenesis of Hashimotos thyroiditis in children Artur Bossowski Received Received
  2-RFC4 Data mining and computational analysis of human growth hormone gene (GH1) sequence in normal population to identify potential variants with disease-causing effects. Sonia Verma Received Received
  2-RFC1 Changes in CYP19A1 and CYP3A4 activities due to population genetic variations in human P450 Oxidoreductase Shaheena Parween Received Received
  2-RFC9 Novel variant in GNRHR gene regulatory region in a pedigree with maternally inherited precocious puberty Magdalena Avbelj Stefanija Received Received
  2-P2 GnRH-analogue treatment in children with congenital adrenal hyperplasia (CAH): data from a multicenter CAH registry Eva Hortas Received Received
  2-RFC7 Outcomes of a quality improvement project integrating Continuous Glucose Monitoring Systems into the routine management of neonatal hypoglycaemia Sinead McGlacken-Byrne Received Received
  2-RFC12 Bone mineral density is increased in 276 Danish children and adolescents with Type-1-Diabetes. Jens Otto Broby Madsen Received Received
  3-RFC2 Measured free 25-hydroxyvitamin D in healthy children and relationship to total 25-hydroxyvitamin D, calculated free 25-hydroxyvitamin D and vitamin D binding protein Laura Bosch i Ara Received Received
  3-LB Glycemic Impact of Long Term Use of Diazoxide Choline Controlled-Release Tablets in Patients with Prader-Willi Syndrome or with Very High Triglycerides Neil Cowen Received Received
  3-RFC12 BARRIERS AND SOURCES OF SUPPORT FOR THE PERFORMANCE OF PHYSICAL ACTIVITY IN PEDIATRIC TYPE 1 DIABETES Michal Cohen Received Received
  3-RFC11 Increased levels of bone formation and resorption markers in patients with hypophosphatemic rickets. Signe Sparre Beck-Nielsen Received Received
  3-RFC6 Effect of the Melanocortin-4 Receptor Agonist, Setmelanotide, on Obesity and Hyperphagia in Individuals Affected by Bardet-Biedl Syndrome Katie Fleming Received Received
  3-RFC3 Significant prevalence of severe monogenic immune defects among children with Type 1 diabetes and low T1D-genetic risk score Stepanka Pruhova Received Received
  3-RFC1 Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction Avinaash Maharaj Received Received
  3-P3 Nelsons syndrome after bilateral adrenalectomy for Cushings Disease in pediatric age report of a case Catarina Machado Received Received
  3-RFC8 Pharmacological treatment of adolescent Polycystic Ovary Syndrome (PCOS) according to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS Alexia Pena Received Received
  3-RFC5 Incidence and treatment outcome of childhood thyrotoxicosis Maria Lodefalk Received Received
  3-RFC13 CIRCULATING MKRN3, KISSPEPTIN AND IGF-1 LEVELS IN GIRLS DURING THE CLINICAL ONSET OF PUBERTY. Lixue Ouyang Received Received
  3-P1 Effects of pre- and postnatal glucocorticoid exposure on the cognitive function of children and adolescents with congenital adrenal hypeplasia Valeria Messina Received Received
  3-RFC15 Multiple pituitary hormone deficiencies and early onset obesity in two siblings with a mutation in the MAGEL2-gene. Evidence for an important regulatory function of the MAGEL2-gene in the hypothalamic-pituitary hormone pathways. Ursula Kuhnle-Krahl Received Received
  3-RFC14 Dysregulated glucose homeostasis in Congenital Central Hypoventilation Syndrome Yassmin Musthaffa Received Received
  3-RFC7 Central venous cathether-associated thrombosis in children with congenital hyperinsulinism Daphne Yau Received Received
  3-RFC9 What is the best parameter to decide the initial dose of depot leuprolide acetate in girls with idiopathic central precocious puberty? Dogus Vuralli Received Received
  3-RFC10 Developmental regulation of obestatin and adropin in Prader-Willi syndrome and non-syndromic obesity: associations with weight, BMI-z, HOMA-IR, and lipid profile Camila Orsso Received Received
  3-P2 Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia: a systematic Cochrane review Sze Ng Received Received
  4-RFC7 EXPRESSION OF MIR-576-5p IN UMBILICAL CORD AS A NOVEL BIOMARKER FOR THE IDENTIFICATION OF CATCH-UP GROWTH IN SMALL-FOR-GESTATIONAL-AGE INFANTS Abel Lopez-Bermejo Received Received
  4-RFC10 Comparative analysis between immunoassay and tandem mass spectrometry for androgens before and after human recombinant gonadotrophin in children with genital ambiguity and 46,XY karyotype LETÍCIA DE OLIVEIRA Received Received
  4-RFC6 Functionality and phenotypic characteristics of mutations in the human leptin receptor Adriana Nunziata Received Received
  4-RFC15 Characteristics, effectiveness and safety data from clinically relevant subgroups of patients with severe IGF-I deficiency: results from the European Increlex Growth Forum Database registry Joachim Woelfle Received Received
  4-RFC12 Use of telemonitoring via a mobile device app reduces HbA1c in type 1 diabetic children and adolescents Philippe Klee Received Received
  4-RFC1 Mass spectrometry-based assessment of childhood androgen excess in 487 consecutive patients over 5 years Jan Idkowiak Received Received
  4-RFC5 The value of cytological, histological and US examination to determine of management children with nodular goiter Alexander Anikiev Received Received
  4-P3 Basal levels of 17-hydroxyprogesterone can distinguish isolated precocious pubarche from non-classical congenital adrenal hyperplasia in children: a prospective observational study anna grandone Received Received
  4-RFC2 Novel severe skeletal dysplasia with under-mineralisation associated with reduced in utero calcium transport and TRPV6 compound heterozygous variants Philippa Bowen Received Received
  4-P1 Carriers of CYP21A2 mutations have decreased mortality in infectious diseases, anational population registry study Anna Nordenstrm Received Received
  4-RFC3 Functional characterization of a novel KLF11 mutation identified in a family with autoantibody-negative type 1 diabetes Kikumi Ushijima Received Received
  4-RFC4 A longitudinal study on miRNAs circulating levels in a cohort of SGA and AGA subjects, evaluated during childhood and young adulthood elena inzaghi Received Received
  4-RFC9 REplacement of MAle mini-Puberty in neonates and children with micropenis and cryptorchidism due to hypogonadotropic hypogonadism. Results of the REMAP study ISRCTN13007297. Dimitrios T. Papadimitriou Received Received
  4-RFC13 Gain in predicted adult height using the combination of an LHRH analogue and an aromatase inhibitor in early maturing girls with compromised growth for 2 yrs or until the age of 11 is maintained and further improved by aromatase inhibitor monotherapy. Results on final height of the GAIL study ISRCTN11469487. DIMITRIOS T. PAPADIMITRIOU Received Received
  4-RFC8 Establishing age, sex, and method related reference ranges for anogenital distance - a marker of in utero androgen action Marie Lindhardt Ljubicic Received Received
  4-RFC11 A new form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency caused by abolished Store-Operated Ca2 Entry Mario Cuk Received Received
  4-LB An updated evolutionary study in Glucocorticoid receptors; insights from a comprehensive phylogenetic, SNPs and mutations analysis of the Nuclear receptors family.An updated evolutionary study in Glucocorticoid receptors; insights from a comprehensive p Louis Papageorgiou Received Received
  4-P2 Hydrocortisone (HC) dose in children with congenital adrenal hyperplasia (CAH) Heike Hoyer-Kuhn Received Received
  4-RFC14 A novel germline DICER1 mutation in a girl with multinodular goiter and ovarian Sertoli-Leydig cell tumor. katarina Gluic Received Received
  5-RFC15 Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths Bradley Miller Received Received
  5-RFC2 Identification of characteristic neurological complications in infants with Achondroplasia by routine MRI screening. Harry Dougherty Received Received
  5-P3 Age at diagnosis and outcome in Maghreb patients with 21-hydroxylase deficient congenital adrenal hyperplasia; urgent need for newborn screening Asmahane Ladjouze Received Received
  5-RFC4 12-Month effects of once-weekly and twice-monthly administration of hybrid Fc-fused human growth hormone, GX-H9, treatment in pediatric with GHD deficiency Sang Yoon Lee Received Received
  5-RFC8 Latest progress in tissue engineered urethral regeneration. From rabbit to dog, a step from human clinical trial for surgical treatment of VSD (Variation of Sex Development). Kalitha Pinnagoda Received Received
  5-RFC11 The Determinants Of Skeletal Fragility In Children With Type 1 Diabetes Mellitus Suet Ching Chen Received Received
  5-RFC7 Alteration of Renal Corticosteroid Signaling Pathways in Preterm Infants: Neonatal Adaptation and Developmental Programming of Hypertension. Laurence Dumeige Received Received
  5-RFC3 Recent changes in the pre- and postnatal growth trajectories of Offspring from Gestational Diabetic Mothers Laurentya Olga Received Received
  5-RFC1 Quantitative urinary GC-MS based steroid analysis for treatment monitoring of adolescents and young adults with autoimmune primary adrenal insufficiency Clemens Kamrath Received Received
  5-P2 Perioperative Care of CAH Incongruencies of Practices among Canadian Specialists Munier Nour Received Received
  5-LB ASSOCIATION BETWEEN THE USE OF ANTENATAL STEROIDS FOR LUNG MATURATION AND HYPOGLYCEMIA IN NEWBORNS BETWEEN 26 AND 34 6/7 WEEKS OF GESTATION. Gina Marcela Gonzalez Valencia Received Received
  5-RFC6 High-throughput untargeted plasma metabolomics unravels gender dimorphic metabolic trajectories in naturally conceived and ICSI prepubertal children Alexandra Gkourogianni Received Received
  5-RFC12 Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes Konstantina Mouzaki Received Received
  5-P1 Adrenal steroid precursors with glucocorticoid activity are able to preventadrenal crises in untreated congenital adrenal hyperplasia (CAH) patients Manon Engels Received Received
  5-RFC14 Natural course of MEN type 2B syndrome; a Dutch single-center cohort. Annemarie Verrijn Stuart Received Received
  5-RFC5 Evidence for a founder effect in Multiple Endocrine Neoplasia 2 Vassos Neocleous Received Received
  5-RFC9 Non-isolated central precocious puberty: prevalence of brain lesions and other associated disorders Selmen Wannes Received Received
  5-RFC13 Pubertal voice break: Temporal relation of secondary sexual characteristics in healthy boys Alexander Siegfried Busch Received Received
  6-RFC10 Effect of Phosphate and Vitamin D analogues of X-Linked Hypophosphatemia during growth on the development of osteoarticular lesions in the Hyp mouse model Axelle Cauliez Received Received
  6-RFC14 Identification of epithelial sodium channel (ENaC) in endometrial pipelle biopsy samples Aaron Hanukoglu Received Received
  6-RFC12 AMGLIDIA, a suspension of glibenclamide for patients with neonatal diabetes, long term data on efficiency and tolerance jacques beltrand Received Received
  6-RFC5 DUOX2 Deficiency in Quebec: From Life-threatening Compressive Goiter in Infancy to Lifelong Euthyroidism Gabrielle Dufort Received Received
  6-RFC2 The novel R211Q POP1 homozygous mutation causes severe short stature but uniquely only subtle skeletal dysplasia Maha Abdulhadi-Atwan Received Received
  6-RFC1 A laboratory harmonization strategy for steroid hormone profiling by MoM-transformed, normalized reference ranges independent of age-, sex -and units Alexandra Kulle Received Received
  6-RFC3 Treatment adherence and weight loss are key predictors of HbA1c one year after diagnosis of childhood Type 2 Diabetes in UK Toby Candler Received Received
  6-P2 Analysis of phenotypes and genotypes in 84 patients with 21-hydroxylase deficiency Lele Hou Received Received
  6-RFC4 Effect of 2 years of Growth Hormone Treatment on Glucose Tolerance in Adults with Prader-Willi Syndrome Layla Damen Received Received
  6-RFC15 Latest results from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope in children requiring growth hormone treatment Shankar Kanumakala Received Received
  6-P3 An adrenal tumor presenting as a premature pubarche in a 7 year-old girl. Marie-Neige CAMPAS Received Received
  6-LB Sex hormone levels in young children: a pilot study of the Japan Environment and Childrens Study Tadayuki Ayabe Received Received
  6-P1 Genome-wide investigation of DNA Methylation in peripheral T-cells from patients with CAH Leif Karlsson Received Received
  6-RFC11 Reference Values of Automated Bone Age and Bone Health Index for Mexican children and adolescents. América Liliana Miranda Lora Received Received
  6-RFC7 Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases FLAVIA NAPOLI Received Received
  6-RFC9 CAN NEUROIMAGING PREDICT ENDOCRINE MORBIDITY IN CONGENITAL HYPOTHALAMO-PITUITARY (H-P) DISORDERS? Manuela Cerbone Received Received
  6-RFC13 Close correlation between salivary and blood steroids in normal boys: Salivary testosterone best characterizes male puberty Katarina Gluic Received Received
  7-P3 Refractory Cyclical Cushings Disease - A case of multiple pituitary micro-adenomas in a three year old girl after 8 years follow up Carl Leith van Heyningen Received Received
  7-P2 Miscarriages in families with a child with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) Theresa Penger Received Received
  7-LB Mutational analysis of SRD5A2 and AR genes in Indian children with 46 XY disorders of sex development Vandana Jain Received Received
  7-P1 Birth Incidence, Age at diagnosis, Mortality in Congenital Adrenal Hyperplasia in Korea: A Nationwide Population-Based Study Jihyun Kim Received Received
  8-P1 Impact of puberty on final height in children and adolescents with congenital adrenal hyperplasia (CAH) Julia Rohayem Received Received
  8-P3 Topical corticosteroid-induced adrenal insufficiency Chiraz Ghaddhab Received Received
  8-P2 Testing antiandrogens and aromatase inhibitors to achieve normal growth in children with classical congenital adrenal hyperplasia: A systematic review and meta-analysis Al Balwi Rana Received Received
  8-LB Pharmacokinetics of Diazoxide Choline Controlled-Release Tablets, a Once Daily Treatment Being Evaluated in Patients with Prader Willi Syndrome Parisa Salehi Received Received
  9-P3 Early diagnosis of Duchenne muscular dystrophy in 6-months-old male with primary adrenal insufficiency Eda Yanar Received Received
  9-P1 The relationship of baseline, incremental and peak cortisol following a Short Synacthen Test single-centre analysis of three years data. Charlotte Elder Received Received
  9-LB Two siblings with congenital syndromic hypopituitarism and TBC1D32 mutations Johanna Hietamki Received Received
  10-P1 The circadian rhythm of cortisol binding globulin has little impact on cortisol exposure after hydrocortisone dosing Richard Ross Received Received
  10-P3 LIPOID ADRENAL HYPERPLASIA DIAGNOSED WITH SEVERE CHOLESTASIS IN NEWBORN emel hatun aytac kaplan Received Received
  10-LB The influence of oil-soluble iodinated contrast medium (Lipiodol) on childs thyroid function in mice Tadashi Hongyo Received Received
  11-LB Metabolic profile in survivors of pediatric hematopoietic stem cells transplantation after chemotherapy-only conditioning LUMINITA-NICOLETA CIMA Received Received
  11-P1 Characterizing the Steroidome in Amniotic Fluid of Mid-Gestation by LC-MS/MS Rong Wang Received Received
  11-P3 Severe hyponatraemia with absence of hyperkalaemia in a patient with Addisons disease Hakan Dneray Received Received
  11-P2 Neonatal screening for congenital adrenal hyperplasia in Turkey: a pilot study with 38,935 infants TULAY GURAN Received Received
  12-LB Disrupting the Norm: The experience of young people with DSD Esko Wiltshire Received Received
  12-P2 Autoantibodies against 21-hydroxylase in prediction of adrenal failure in APECED patients. Leila Sozaeva Received Received
  12-P3 Deep bronze skin without sun exposition in a 16-year old girl Hildegard Jasser-Nitsche Received Received
  12-P1 Pediatric Adrenocortical Tumors. A single tertiary center experience: Clinical, Biological and Pathologic Characteristics Analysis. Maria Celeste Mattone Received Received
  13-P3 Case of primary pigmented nodular adrenocortical Huyen Tran Received Received
  13-LB Clinical and endocrine characteristics and genetic analysis of Korean children with McCuneAlbright syndrome Minji Im Received Received
  13-P2 A first combination case of 21-hydroxilase deficiency and CHARGE syndrome confirmed by genetic analysis Miyuki Kitamura Received Received
  14-P1 MOLECULAR CHARACTERIZATION OF TNXA/TNXB CHIMERAS IN CYP21A2 GENE DELETIONS: HIGH FREQUENCY OF UNDIAGNOSED EHLERS-DANLOS SYNDROME IN CONGENITAL ADRENAL HYPERPLASIA PATIENTS Roxana Marino Received Received
  14-P3 Two Case Report of Adrenocortical Adenoma Huyen Tran Received Received
  14-LB BETA-CELL FUNCTION IN CHINESE YOUNGSTERS WITH TYPE 1 DIABETES AND ASSESSMENT OF SURROGATE MARKERS OF SEVERE INSULIN DEFICIENCY Jinna Yuan Received Received
  14-P2 Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients Melek Yildiz Received Received
  15-P2 Study of Cardiovascular Risk Factors and Carotid Intima-media Thickness in Children with Congenital Adrenal Hyperplasia Shaymaa Elsayed Received Received
  15-P3 A HOMOZYGOUS MUTATION c.518TA (p.lle173Asn) OF THE CYP21A2 GENE PRESENTING AS NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA (NCAH) Iva Stoeva Received Received
  15-P1 New insights into Low Dose Dexamethasone Suppression Test in paediatric Cushings Syndrome (CS) Ingrid Wilkinson Received Received
  16-LB Successful treatment of Alopecia Totalis with calcitriol and paricalcitol in two girls aged 3 and 7-years Eleni Dermitzaki Received Received
  16-P1 Recurrent hypoglycemia in a preschooler girl with overgrowth: Isolated ACTH-deficiency with a novel TPIT mutation ZEHRA YAVAS ABALI Received Received
  16-P3 Adrenals and HPA axisa; Atypical presentation of adrenal insufficiency. Khalid Khan Received Received
  16-P2 The spectrum of genetic defects in Congenital Adrenal Hyperplasia in the population of Cyprus: A retrospective analysis NICOS SKORDIS Received Received
  17-LB Protein-Induced Hypoglycemia Secondary to Hyperinsulinism-Hyperammonemia (HI/HA) Syndrome: a GLUD1 Gene Mutation Fabiola DAmbrosio Received Received
  17-P2 Childhood Growth Advancement in Girls with Premature Adrenarche Heralds Anabolic Effects by Adulthood Jani Liimatta Received Received
  17-P3 Non-classic congenital adrenal hyperplasia causing alleles among adolescent girls with PCOS genetical study. Lasma Lidaka Received Received
  17-P1 Biochemical, genetic and molecular characterization of a novel P399_E401Dup mutation in P450 oxidoreductase (POR) altering several enzymatic activities in a patient with a 46,XX DSD phenotype at birth Claudia Boettcher Received Received
  18-P1 Unfavorable hormonal and psychologic profile in adult women with a history of premature adrenarche (PA) and pubarche (PA) but not thelarche:Similarities with and differences from women with PCOS Christina Bothou Received Received
  18-P2 Title: A Novel Mutation in the MC2R Gene in a Two-Year-Old Boy with Adrenal Insufficiency Katarina Gluic Received Received
  18-P3 Adequate interpretation of cortisol levels in children Maria J. Chueca Received Received
  19-P3 ERYTHROCYTOSIS AS FIRST MANIFESTATION OF ADRENAL MASS Mariella Valenzise Received Received
  19-P2 Two cases of apparent mineralocorticoid excess due to novel mutations in HSD11B2 gene Nina Makretskaya Received Received
  19-P1 The usefulness of combined analysis of serum and salivary maximum cortisol response to low-dose ACTH test to define the requirement of hormone replacement treatment. Elisa Vaiani Received Received
  19-LB Characterization and clinical course of prolactinoma in Korean adolescents Minji Im Received Received
  20-P3 A neonatal case with Familial Glucocorticoid Deficiency Type 1 having adrenal crisis in early period Mehmet Keskin Received Received
  20-LB The efficacy and safety of octreotide treatment for diazoxide-unresponsive congenital hyperinsulinism in China Bingyan Cao Received Received
  20-P2 Long-term follow-up of safety and disease control for hydrocortisone granules designed to give age-appropriate dosing with taste masking to children with adrenal insufficiency Uta Neumann Received Received
  20-P1 High DHEAS (HD) in girls determines earlier pubertal maturation and mild hyperandrogenism throughout pubertal development Veronica Mericq Received Received
  21-P1 HIGHER DEHYDROEPIANDROSTERONE LEVELS IN PREPUBERTAL CHILDREN BORN VERY PRETERM Veronica Mericq Received Received
  21-P2 Borderline peak plasma cortisol following Synacthen stimulation single-centre analysis of three years data. Sarah Burn Received Received
  21-P3 Presenting features, clinical characteristics and follow up of familial isolated glucocorticoid deficiency (FGD) due to mutations in MC2R and MRAP genes Mehmet Nuri Ozbek Received Received
  22-P3 Identification of X-linked adrenoleukodystrophy in boys presenting with adrenal insufficiency in the absence of adrenal antibodies Michelle Kinahan Received Received
  22-P2 Unilateral Adrenalectomy for primary pigmented nodular adrenocortical disease causing Cushing Syndrome Shinji Higuchi Received Received
  22-P1 A large consanguineous family with a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation in the SCNN1A gene: functional studies Alexandra Efthymiadou Received Received
  23-P2 Adrenal crisis in children with adrenal insufficiency: prevalence and risk factors Ori Eyal Received Received
  23-P3 Secondary hyperaldosteronism in the course of Cystic Fibrosis Michal Erazmus Received Received
  23-P1 Associations between maternal and offspring hair cortisol concentrations and child behavioral symptoms in pairs of children 18-48 months old and their mothers with and without perinatal mental disorders ANNA AGAPAKI Received Received
  24-P1 Gonadotropin-Dependent Pubertal Disorders are Common in Patients with Virilizing Adrenocortical Tumors in Childhood Stecchini Monica Received Received
  24-P2 The effectiveness of a Stress-Management Intervention Program in behavioral parameters and hair cortisol concentrations in children with Attention Deficit Hyperactivity Disorder Gerasimos Makris Received Received
  24-P3 The P30L mutation in the CYP21A2 gene in a girl with congenital adrenal hyperplasia with hidden salt loosing and central precocious puberty Natallia Akulevich Received Received
  25-P3 Congenital adrenal hyperplasia due to a rare homozygous mutation R483P in the CYP21A2 gene and coexisting growth hormone deficiency Natallia Akulevich Received Received
  25-P2 Very high dehydroepiandrosterone sulfate (DHEAS) in serum of an overweight female adolescent without a tumor Daniel Iliev Received Received
  26-P1 Duration of breastfeeding and bone mineral density in childhood- a prospective study among preschool children MYA THWAY TINT Received Received
  26-P2 Early recognition of adrenal insufficiency after hematopoietic stem cell transplantation during childhood Yujung Choi Received Received
  26-P3 Rare Case of Androgen Producing Tumor in 14 Month Old Girl Nino Kheladze Received Received
  27-P2 Reference values for serum 17-alfa hydroxyprogesterone and adrenal size in healthy newborns Glay Karagzel Received Received
  27-P1 Bone health in adolescents born small for gestational age (SGA) Indre Petraitiene Received Received
  27-P3 Adrenocortical tumours in children a case series Rashida Farhad Vasanwala Received Received
  28-P2 A rare case of ACTH- independent Cushings syndrome due to bilateral micronodular adrenal hyperplasia and myoclonic dystonia IOANNIS- ANARGYROS VASILAKIS Received Received
  28-P1 Longitudinal study of bone mass in Swedish children treated with modified ketogenic diet Anna Svedlund Received Received
  28-P3 DISCRETE VIRILIZATION IN GIRLS WITH THE CLASSIC FORM OF CONGENITAL ADRENAL HYPERPLASIA: THE IMPORTANCE OF A DETAILED GENITAL EXAMINATION AT BIRTH Sofia Helena Valente Lemos-Marini Received Received
  29-P1 Fracture epidemiology for children in Western Australia between 2005-2015: do we need to be concerned about bone health? Aris Siafarikas Received Received
  29-P3 A New Methodology for Early Identification of Steroid Resistant Acute Graft-Versus-Host Disease Patients Steven Ghanny Received Received
  29-P2 Two siblins and three cousins with Allgrove( 4A syndrome) syndrome in a Turkish family. : A novel mutation in the aladin gene. Aysehan Akinci Received Received
  30-P1 Bone biochemistry in children with fractures presenting with suspected non-accidental injury Owen Forbes Received Received
  30-P3 Delayed diagnosis of a patient with Antley-Bixler Syndrome TARIK KIRKGOZ Received Received
  30-P2 Ganglioneuroma presenting as an adrenal incidentaloma in a 10-year-old boy-a rare entity MEGHNA CHAWLA Received Received
  31-P3 Growth hormone treatment of 2 patients with X-linked hypophosphatemic rickets caused by PHEX mutation: effects on linear growth Aleksandra Rojek Received Received
  31-P1 Systematic Screening Using DXA Lateral Vertebral Morphometry Is Associated With A High Prevalence Of Vertebral Fractures In Duchenne Muscular Dystrophy: Results from ScOT-DMD study Shuko Joseph Received Received
  32-P2 Adrenal hypoplasia seemingly first as a primary hypoaldosteronism Silvia Ciancia Received Received
  32-P3 A NOVEL HOMOZYGOUS MUTATION IN THE CASR GENE IN A NEONATE WITH SEVERE PRIMARY HYPERPARATHYROIDISM ; A CASE REPORT. Ali Alqadi Received Received
  32-P1 Bone mineral density and glycemic control in children and adolescents with type 1 diabetes mellitus Gitte Fuusager Received Received
  33-P1 Comparison of manual and automated bone age assessment in 1285 children and adolescents aged 5 to 16 years. Klara Maratova Received Received
  33-P3 A 13 Year-Old Boy Diagnosed As Osteogenesis Imperfecta With Normal Bone Mineral Density Berna Filibeli Received Received
  33-P2 Quantitative ultrasound evaluation in a cohort of 43 young adults with classical CAH due to 21-hydroxylase deficiency (21OHD): is bone mineral quality impaired? Federico Baronio Received Received
  34-P1 Is Plasma C-Type Natriuretic Peptide Level Available for Typing and Diagnosis of Skeletal Dysplasia Cases? Sukran Darcan Received Received
  34-P3 A rare cause of hypercalcemia in childhood: hypercalcemia associated with parathormon-related peptid Berna Filibeli Received Received
  35-P3 Our Treatment Experience with Nocturnal Continuous Enteral Calcium Infusion in a Case with Vitamin D Resistance Rickets Type II Berna Filibeli Received Received
  35-P1 Long-term Outcomes of Osteogenesis Imperfecta in the Bisphosphonate Era margaret zacharin Received Received
  36-P1 Novel LRP5 loss-of-function mutation causes Osteoporosis-pseudoglioma syndrome Débora Braslavsky Received Received
  36-P2 Length estimation based on clinical and anthropometric measures in newborns. Martha Baauregard.Paz Received Received
  37-P1 Hypercalcaemia after treatment with Denosumab in children: Bisphosphonates as an option for therapy and/or prevention? Carmen Sydlik Received Received
  37-P2 VITAMIN D DEFICIENT ( NUTRITIONAL) RICKETS PRESENTING IN INFANCY Gangoda Liyanage Dilusha Chaturani Prematilake Received Received
  37-P3 Hypophosphatemic Hypercalciuric Ricket: 3 brothers with Dents Disease. Claudia Godoy Received Received
  38-P2 The Effect Of Vitamin D Receptor Polymorphism On Bone Mineral Density in Egyptian Patients With Beta Thalassemia Major Omneya Omar Received Received
  38-P1 Disease Burden and Systemic Manifestations of HPP in Children Enrolled in the Global HPP Registry Megan Cowell Received Received
  39-P1 3-epi-25 serum 25-hydroxyvitamin D3 concentrations in Chilean children between 5 and 8 years Cristian Seiltgens Received Received
  39-P2 Vitamin D in adolescents: a comprehensive review of guidelines and recommendations Magdalini Patseadou Received Received
  39-P3 Carbonic anhydrase deficiency: Three Siblings Derya Bulus Received Received
  40-P3 A novel p.Gly775Glu missense COL1A2 mutation causes severe osteogenesis imperfecta in a prepubertal girl. Eleni Kotanidou Received Received
  40-P2 X-Linked Hypophosphatemia Registry an international prospective patient registry Raja Padidela Received Received
  40-P1 Poor metabolic control in children and adolescents with type 1 diabetes and psychiatric comorbidity Grete Teilmann Received Received
  41-P2 Clinical and Biological Parameters Associated to the Severity of X-linked Hypophosphatemia in Children Anya Rothenbuhler Received Received
  41-P3 SHOX gene deletion screening by FISH in children with short stature and characteristics of patients Erdal Kurnaz Received Received
  41-P1 Concealment of Type 1 Diabetes in Adolescence Affects Adherence to Treatment, Metabolic Control, and Quality of Life Judith Nir Received Received
  42-P2 High Fibroblast Growth Factor (FGF) 23: An Unusual Cause of Severe Osteoporosis in a Patient with Chronic Liver Disease Nicholas Beng Hui Ng Received Received
  42-P3 Pseudoachondroplasia emine demet akba&351; Received Received
  42-P1 RISKY BEHAVIORS OF ADOLESCENTS WITH TYPE 1 DIABETES IN COMPARISON WITH THEIR HEALTHY PEERS Betina Kandyla Received Received
  43-P1 The effect of social burden on paediatric diabetes outcomes Madalena Sales-Luis Received Received
  43-P2 Metabolic syndrome in children with X-linked hypophosphatemic rickets (XLHR) Anne-Sophie Lambert Received Received
  43-P3 LOW LEVEL OF VITAMIN D IN CHILDREN INCREASES THE RISK OF BONE FRACTURES. Georges Nicolas Received Received
  44-P1 Parental anxiety about hypoglycemia of children and adolescents with type 1 diabetes mellitus (T1DM) and the associated factors. Evangelia Ntinou Received Received
  44-P2 High incidence of Cranial Synostosis and Chiari Malformation in Children with X-linked Hypophosphatemic rickets Anya Rothenbuhler Received Received
  44-P3 Clinical Evaluation of Eight Patients with Parathyroid Adenoma GUL D&304;REK Received Received
  45-P3 Idiopathic hypoparathyroidism in a 10 year-old girl with concomitant epilepsy, Long Q-T Syndrome (LQTS), pericarditis and pneumonia. Hanna Borysewicz-Sa&324;czyk Received Received
  45-P2 AN UNUSUAL CASE OF HYPOPHOSPHATEMIA IN A CHILD AFFECTED BY DI GEORGE SYNDROME Mila Kalapurackal Received Received
  45-P1 Management of Diabetes During Ramadan Fasting in Children and Adolescents: Survey of Physicians Perceptions and Practices in the Arab Society of Paediatric Endocrinology and Diabetes (ASPED) countries Nancy Elbarbary Received Received
  46-P2 Novel SLC34A1 mutation in a girl infant with idiopathic infantile hypercalcemia seok jin kang Received Received
  46-P1 Phenotypes of diabetes and determinants of glycemic control and diabetes complications in Haitian youth living in Haiti Marie-Pier Dumas Received Received
  47-P1 SMOKE EXPOSURE AND CARDIO-METABOLIC PROFILE IN YOUTH WITH TYPE 1 DIABETES Valeria Calcaterra Received Received
  47-P2 A Novel Variant of SLC34A1 Gene in an Infant with Idiopathic Infantile Hypercalcemia Gi-Min Lee Received Received
  47-P3 Evaluation of Bone Mineral Density and Bone Metabolism Markers in Children Diagnosed as Celiac Disease Havva Nur Peltek Kendirci Received Received
  48-P2 Infantile Arterial Calcification and Subsequent Hypophosphatemia Due to ENPP1 mutation A case followed through to adulthood Munier Nour Received Received
  48-P1 Menstrual cycle disorders in young women with type 1 diabetes mellitus Ioanna Kosteria Received Received
  49-P2 Pediatric Quality Of Life Inventory In Children With Osteogenesis Imperfect In Dr Soetomo Hospital Surabaya nur rochmah Received Received
  49-P1 Life changing decisions due to etiological genetic diagnosis in families of children with Maturity Onset Diabetes of the Young (MODY). Gherta Bril Received Received
  49-P3 Evaluating the effect of zoledronic acid on treatment of primary and secondary pediatric osteoporosis at Childrens Hospital 1 in Vietnam Huyen Tran Received Received
  50-P1 NBAS gene mutation causes Insulin-dependent Diabetes Mellitus in a patient with a multisystem disorder consisting immunodeficiency and extremely short stature SOFIA GIATROPOULOU Received Received
  50-P2 Osteoporosis-pseudoglioma Syndrome (OPPG): Improvement of Osteoporosis on Biphosphonate Therapy Esin Karakilic-Ozturan Received Received
  50-P3 Hypocalcemia secondary to maternal vitamin D deficiency Khalid Khan Received Received
  51-P1 Identification of six novel mutations in monogenic diabetes and congenital hyperinsulinism and detected by targeted-exome sequencing in Korea CHONG KUN CHEON Received Received
  52-P3 A rare case of familial hypocalcemia. Leila Sozaeva Received Received
  52-P1 Genetic susceptibility to Type 1 Diabetes in children: analysis of polymorphisms rs1990760 - IFIH1, rs20541 - IL13 , rs231775 - CTLA 4 Aleksandra Goralczyk Received Received
  52-P2 Evaluation of bone mineral density in a cohort of children with Growth Hormone deficiency Valentina Cenciarelli Received Received
  53-P1 Neonatal diabetes as a first symptom of IPEX syndrom Agnieszka Brandt-Varma Received Received
  53-P3 HDR Syndrome: A Case Report of Hypoparathyroidism, Hearing Loss and Renal Agenesis Mihaela Dimitrova-Mladenova Received Received
  53-P2 Follow-up on bone health in children with acute lymphoblastic leukemia (ALL) Hamilton Cassinelli Received Received
  54-P1 CpG methylation status changes within the protein tyrosine phosphatase non-receptor type 22 gene promoters in children and adolescents of Greek origin with Type 1 diabetes Konstantina Mouzaki Received Received
  54-P2 Effect of Pubertal inductionn bone mass accrual, in adolescent boys with Duchenne muscular dystrophy Margaret Zacharin Received Received
  54-P3 Growth in the coeliac disease of the child Mimouna Bessahraoui Received Received
  55-P3 The British OsteoNEcrosis Study: A Multi-Centre Prospective Study Nadia Amin Received Received
  55-P1 Wolfram Syndrome case with hypergonadotropic hypogonadism: A novel mutation ZEYNEP UZAN TATLI Received Received
  56-P3 Response to pamidronate therapy and pharmacogenetics in patients with Osteogenesis Imperfecta Nalini M Selveindran Received Received
  56-P2 First reported cases of a novel variant of GNAS 1 gene Argyro Panagiotakou Received Received
  56-P1 Different Clinical Findings in Maturity Onset Diabetes of The Young due to B-Lymphocyte Kinase Gene Mutations Ayla Guven Received Received
  57-P1 Three New Gene Variants(PTPRD, SYT9, and WFS1) related to Korean MODY Children Decrease Insulin Secretion in Human Pancreatic Beta Cells Kyung-Mi Jang Received Received
  57-P2 AN UNUSUAL CAUSE OF SHORT STATURE Serap Turan Received Received
  57-P3 Results of 22 weeks of burosumab therapy in a patient with severe bone deformities due to XLH Pablo Ruiz-Ocaña Received Received
  58-P1 Comprehensive genetic testing shows one in five children with diabetes and non-autoimmune extra-pancreatic features have monogenic aetiology Kashyap Patel Received Received
  58-P3 Severe neonatal hypercalcemia: a challenging case Raihana Hashim Received Received
  58-P2 Validation of an automated method (BoneXpert) for the determination of bone age in paediatric endocrinology - A single centre experience Antonia Dastamani Received Received
  59-P3 Assessment of Vitamin D Status in Healthy Pre-pubertal Egyptian Children Rasha Hamza Received Received
  59-P2 Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism emine demet akba&351; Received Received
  59-P1 Impact of diabetes during pregnancy in women affected with GCK-MODY on neonatal health outcome. Agnieszka Brandt-Varma Received Received
  60-P2 Incidence of Childhood Type 1 and Type 2 Diabetes Mellitus in Qatar between 2012- 2016 ASHRAF TAWFIK SOLIMAN Received Received
  60-P3 Are Caucasian children at risk of sub-optimal vitamin D levels? Krutika Shrikhande Received Received
  61-P3 Incidence of vitamin D deficiency in 12-year old children in Japan Satomi Koyama Received Received
  61-P2 The Prevalence of Double Diabetes in Children and Adolescents in Qatar Ashraf Soliman Received Received
  61-P1 THE PREVALENCE OF AUTONOMIC AND PERIPHERAL NEUROPATHY IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETIC MELLITUS(T1D) AND ITS ASSOCIATION WITH THE HOMOZYGOUS STATUS OFZ-2/Z-2 POLYMORPHISM OF THE ALDOSE REDUCTASE GENE(AKR1B1) IN THE POLYOL PATHWAY. Charalampos Tsentidis Received Received
  62-P3 Idiopathic Juvenile Osteoporosis: Common Symptoms in an Uncommon Condition SAURABH UPPAL Received Received
  62-P2 Prevalence of Diabetes Type 1 and type 2 in children and adults in Kazakhstan in 2016 Akmaral Nurbekova Received Received
  63-P1 Glucose Intolerance in Survivors of Childhood Hematologic Disorders Seonhwa Lee Received Received
  63-P2 Detection of the pathogenic genes in the diagnosis and treatment of hyperglycemia infants and children Zhuhui Zhao Received Received
  64-P3 Hypercalcemia associated with increased parathyroid hormone-related protein(PTHrP) in a patient with medulloblastoma successfully treated with pamidronate Seok Jin Kang Received Received
  64-P2 Early diagnosis of diabetes type 2 in children with progeria syndromes Martin Bald Received Received
  65-P2 TRANSIENT NEONATAL DIABETES MELLITUS DUE TO NOT DESCRIBED MUTATION IN ABCC8 GEN WITH DIFFERENT BEHAVIOR IN AFFECTED FAMILY MEMBERS IRENE PILAR FERNANDEZ VISERAS Received Received
  65-P1 Evaluation of Diabetes Related complications and Endothelial dysfunction in Adolescents with Type 1 Diabetes Nehad Metwally Received Received
  66-P2 Prothrombin Gene 20210A mutation heterozygosity and MTHFR Gene C677T mutation homozygosity detected in a male toddler experiencing femoral venous thrombosis during diabetic ketoacidosis ANGELIKI KLEISARCHAKI Received Received
  66-P3 A case of Turner syndrome with Graves disease and primary hyperparathyroidism Shigeru Nagaki Received Received
  66-P1 Complexities in the management of New-Onset Diabetes After Transplantation (NODAT) in an adolescent with Senior-Loken syndrome Philippa Bowen Received Received
  67-P2 Pathogenetic heterogeneity of diabetes mellitus in children of Saint-Petersburg city. Mariia Turkunova Received Received
  67-P1 INSULIN RESISTANCE PARAMETERS IN CHILDREN WHO WERE BORN VERY PRETERM AND ADEQUATE FOR GESTATIONAL AGE Hernan Garcia Received Received
  67-P3 Neonatal hypocalcemia revealing a malignant osteopetrosis. Valérie Porquet-Bordes Received Received
  68-P3 Frontal behavior dysfunctions revealing a dramatic progression of complex cranial base abnormalities in a severe osteogenesis imperfecta. Valérie Porquet-Bordes Received Received
  68-P1 Impact on final height of functional insulin-therapy in type 1 diabetes mellitus pediatric patients experience from a Portuguese Pediatric Endocrinology Unit Joana Serra Caetano Serra-Caetano Received Received
  69-P2 Features of Japanese patients with early-onset, MODY-like diabetes without mutations in the major MODY genes. Tohru Yorifuji Received Received
  69-P1 Triglyceride glucose index as a predictor of impaired glucose tolerance in overweight and obese adolescents Voraluck Phatarakijnirund Received Received
  69-P3 Ionized calcium and 25-hydroxyvitamin D3 in children with steroid-sensitive nephrotic syndrome. Yasmine Abdelmeguid Received Received
  70-P1 Birth weight in offsprings of mothers with gestational diabetes mellitus due to mutations in GCK gene. Natalia Zubkova Received Received
  70-P2 Frequency and etiologic spectrum of monogenic diabetes in pediatric diabetes in a single academic center Jin-Ho Choi Received Received
  70-P3 Hypercalcemia due to six newly identified inactivating mutations in the CaSR gene Y&305;lmaz Kor Received Received
  71-P1 Review and Audit of Diabetes Control in Children and Young People with Diabetes Using the FreestyleLibre Flash Glucose Scanning System (FGS) aisha zahid Received Received
  71-P2 Clinical details, Molecular genetic analysis AND Clinical pheonotype correlation of 14 patients with neonatal diabetes from the South India A Single Centre Experience V. SRI NAGESH Received Received
  72-P1 Increasing Use of Continuous Glucose Monitoring (CGM) Among Youth with Type 1 Diabetes (T1D): International comparison of youth from the T1D Exchange (T1DX) and the DPV Initiative Kellee Miller Received Received
  72-P2 SYNDROMIC PATIENTS WITH NEGATIVE ISLET AUTOANTIBODIES SHOULD BE TESTED FOR MONGENIC DIABETES: LESSONS FROM PATIENT WITH TRMT10A MUTATION tu&287;ba etin Received Received
  73-P3 Effects of Diabetes mellitus Type--1..on vitamin D status amomng children .... Katarina Gluic Received Received
  73-P1 Efficacy of Real-Time Continuous Glucose Monitoring in Type 1 Diabetic pre-school and school children treated with Multiple Daily Injections RICCARDO SCHIAFFINI Received Received
  73-P2 Known and a novel mutation in PHKA2 expand the phenotype of glycogen storage disease IXa to include idiopathic ketotic hypoglycaemia Anne Benner Flejsborg Received Received
  74-P2 The application of Next Generation Sequencing MODY Gene Panel in Greek Patients Elizabeth Tatsi Received Received
  74-P1 Catheter site ion and anthropometric measurements at subjects with type 1 diabetes and continuous subcutaneous insulin infusion Maria Xatzipsalti Received Received
  74-P3 Association between prior Toxic Stressors and development of T2DM in Adolescents Adam Adamidis Received Received
  75-P3 First 4 cases of neonatal diabetes from Kazakhstan, Almaty with proven mutations in KCNJ11 and INS genes Akmaral Nurbekova Received Received
  75-P2 TYPE 5 MONOGENIC DIABETES: REPORT OF 7 CASES. Eduard Mogas Viñals Received Received
  75-P1 OPEN SOURCE ARTIFICIAL PANCREAS SYSTEMS USED FROM BULGARIAN CHILDREN AND YOUNG PEOPLE WITH DIABETES Maia Konstantinova Received Received
  76-P1 National Survey of usage of continuous glucose monitoring in children and adolescents at non reimbursed setting Yuliya Bazdarska Received Received
  76-P2 Novel GATA6-mutation in a boy with neonatal diabetes and diaphragmatic hernia.Review of the hereditary cases in the literature Odile Christin Gaisl Received Received
  76-P3 First 2 cases of monogenic diabetes (MODY) from Kazakhstan, Almaty with proven heterozygous mutation in hepatocyte nuclear factor 1-alpha (HNF1A) gene Akmaral Nurbekova Received Received
  77-P2 Clinical and Genetic Characterizations of Maturity Onset Diabetes of The Young: Single Center Results Ayla Guven Received Received
  77-P1 Additional insulin is necessary to prevent rise in blood glucose after fat-protein-rich meals in type 1 diabetes Roland Schweizer Received Received
  78-P2 Protein and fat effects on post - prandial glucose responses among Egyptian children and adolescents with Type 1 diabetes mellitus Noha Arafa Received Received
  79-P1 A Novel SLCA16A1 mutation in An Infant with Hypoglycemia and Severe Metabolic Ketoacidosis. Reem Hasnah Received Received
  79-P2 Amino acids plasma profile in children with type 1 diabetes Teodoro Durá-Travé Received Received
  80-P3 Clinical and Biochemical Characteristics of Familial Type 1 Diabetes Mellitus (FT1DM) compared to Non-Familial Type 1 DM (T1DM). ashraf soliman Received Received
  80-P1 Successful transition to sulfonylurea therapy in infant with neonatal diabetes, developmental delay, epilepsy (DEND syndrome) due to F132L ABCC8 mutation. YULIA TIKHONOVICH Received Received
  80-P2 Betatrophin as a new biomarker of Type 1 Diabetes Mellitus in Paediatrics Laura Bosch i Ara Received Received
  81-P2 Vitamin D status among lraqi children and adolescent with T1DM Mohamed AlAbadi Received Received
  81-P1 ZFP57-associated transient neonatal diabetes is responsive to oral sulfonylurea treatment Christina Reinauer Received Received
  82-P2 IGF-1 relationship with growth velocity in precocious puberty with GnRHa treatment nursel muratoglu sahin Received Received
  82-P3 Clinical Presentation and Autoimmune Markers in Children and Adolescents with Familial Type 1 Diabetes Mellitus (FT1DM) and Familial type 2 Diabetes mellitus (FT2DM) Ashraf Soliman Received Received
  82-P1 The comparison of the occurrence of beta cells autoantibody and regulatory T cells (CD4CD25FoxP3) in patients with type 1 diabetes mellitus, their siblings and healthy children Joanna Sieniawska Received Received
  83-P3 Real world clinical evolution of type 1 diabetes patients on twentyyears Beatriz Garcia Cuartero Received Received
  83-P2 Relation between hypomagnesemia and increased level of HbA1c in patients with diabetes mellitus seok jin kang Received Received
  83-P1 HERV-W-Env protein expression in pediatric type 1 diabetes patients Michael Hauschild Received Received
  84-P1 The comparison of the occurrence of beta cells autoantibody and natural killer cells in patients with type 1 diabetes mellitus, their siblings and healthy children Joanna Sieniawska Received Received
  84-P3 Diabetic capilaropathy: a case report Carlos Andrés Received Received
  84-P2 PID1 alters antilipolytic action of insulin and increases lipolysis via Inhibited the activation of AKT/PKA Pathway chunyan yin Received Received
  85-P2 The Efficacy of Tri-ponderal Mass Index and Body Mass Index in Estimating Insulin Resistance, Hyperlipidemia and Impaired Liver Enzymes During Childhood and Adolescents Ruveyde Bundak Received Received
  85-P1 T and B-Lymphocytes Levels in Children with Type 1 Diabetes in association with Candida infection Stanimira Elkina Received Received
  85-P3 A sibling case of Wolfram syndrome with diabetes mellitus diagnosed within 10 months in early childhood DAI SUZUKI Received Received
  86-P1 Coincidence of Newly Diagnosed Type 1 Diabetes Mellitus with Enteroviruses and Respiratory Tract Viruses Murat Karaoglan Received Received
  86-P3 Continuous Subcutaneous Insulin Infusion in Children and Adolescents:Analysis of Initial and Follow up Basal Rates Damla Gk&351;en Received Received
  87-P1 Investigation into -cell adaptation during puberty Anne-Laure Castell Received Received
  87-P2 Translating the A1C Assay into Estimated Average Glucose Values in Children with Type 1 Diabetes Mellitus Ashraf Soliman Received Received
  87-P3 PREVALANCE OF FATTY LIVER IN PATIENTS WITH TYPE 1 DIABETES MELLITUS ATTENDING DIABETES CLINIC AT ALEXANDRIA UNIVERSITY CHILDRENS HOSPITAL Dina Fawzy Received Received
  88-P2 Relationship between residual endogenous insulin secretion and glycemic control in Japanese children and adolescents with type 1 diabetes. Ikuma Musha Received Received
  88-P3 THE TRIAD OF OBESITY, ACANTHOSIS NIGRICANS AND DIABETES MELLITUS IN A NEWLY DIAGNOSED ADOLESCENT; IS THIS TYPE 1 OR TYPE 2 DIABETES MELLITUS? Dipesalema JOEL Received Received
  88-P1 The shape of the glucose curve and time to glucose peak during an oral glucose tolerance test as indicators of beta cell function in obese adolescents Lavinia La Grasta Sabolic Received Received
  89-P3 A female patient with atypical diabetes features, showing heterozygous mutations on G6PC2 (Glucose 6 phosphatase, catalytic subunit 2). Does explain all clinical manifestations or is it only polymorphism? Elif zsu Received Received
  89-P2 A Curious Case of Persistent Lactic Acidosis in a Child with Diabetic Ketoacidosis Andrew Sng Received Received
  89-P1 FEATURES OF T2DM IN ADOLESCENTS WITH LOW TITER OF ICA AND IAA Irina Eremina Received Received
  90-P2 An unusual case of an exclusively vegan child with diabetic acidosis Maria Xatzipsalti Received Received
  90-P1 Increasing trend of fasting plasma glucose levels and impaired fasting glucose in non-diabetic Korean youth and young adults: A nationally representative population-based study JIEUN LEE Received Received
  90-P3 Clinical and laboratory features at the onset of childhood type 1 diabetes mellitus in the Nortwest region (Trakya) of Turkey Emine Dilek Received Received
  91-P1 Screening for T2D in high risk Egyptian children and adolescents using strip HbA1c and OGTT Noha Musa Received Received
  91-P3 Clinical and Epidemiological Features of Children with Type 1 Diabetes emine demet akba&351; Received Received
  92-P2 Hypertriglyceridemia in Type 1 Diabetes children during Diabetic Ketoacidosis; Relation to DKA severity and Glycemic control. Noha Musa Received Received
  92-P3 Predictors of Optimal Glycemic Control in Children with Diabetes Mellitus Type 1 Receiving Pump Insulin Therapy. Evgeniya Evsyukova Received Received
  92-P1 Association of the sizes and composition of HDL with hepatic steatosis in adolescents with type 2 diabetes (T2D). Jose Antonio Orozco Moales Received Received
  93-P2 Acute mononeuropathy in an 8-year-old-girl with newly diagnosed type 1 diabetes Styliani Giza Received Received
  93-P3 Symptomatic cerebral infarction: A Rare Complication of Diabetic Ketoacidosis Gamze Celmeli Received Received
  93-P1 Functional characterization of novel and known genetic variants in the leptin receptor (LEPR) gene of two patients with morbid obesity Robert Stein Received Received
  94-P3 OUR CLINICAL EXPERIENCES IN TYPE 2 DIABETES gl direk Received Received
  94-P1 Association of single nucleotide polymorphisms in TNFA, PNPLA3, ADIPOQ and APOC3 genes with obesity and non-alcoholic fatty liver disease in north Indian adolescents Vandana Jain Received Received
  94-P2 HLA- G gene promoter methylation status in children and adolescents with Type 1 Diabetes Konstantina Mouzaki Received Received
  95-P2 Impaired adrenal function in pediatric patients with Diabetes Mellitus type 1 evaluated with low-dose Synacthen test MARIALENA KALYMNIOU Received Received
  95-P1 Variation of Circulating Brain-Derived Neurotrophic Factor according to Gender, Body Mass Index and Metabolic Syndrome Parameters in Adolescents FLORA BACOPOULOU Received Received
  95-P3 The relationship between serum levels of C-peptide and the age, body mass index, and inslin doses in newly diagnosed type 1 diabetic children Glay Karagzel Received Received
  96-P2 The incorporation of available technologies for diabetes care among different worldwide centers: The ESPE/ISPAD Working Group on Diabetes Technology Survey Klemen Dovc Received Received
  96-P1 KISSPEPTIN AND THE GENETIC OBESIDOME STYLIANI GERONIKOLOU Received Received
  96-P3 Serum trace element levels in children presenting with diabetic ketozis and diabetic ketoacidosis: A longitudinal controlled study Hakan Dneray Received Received
  97-P3 Evaluation of Relation Between Diabetic Education Levels of Type 1 DM Child/Adolescent and Rarents and Metabolic Control Havva Nur Kendirci Received Received
  97-P2 Higher percentage of insulin pump users at Isle of Man (IOM) Two years observational data Arundoss Gangadharan Received Received
  97-P1 Circulating Exosomal miRNAs Involved in the Pathogenesis of Children Nonalcoholic Steatohepatitis Xuelian Zhou Received Received
  98-P1 PLACENTAL FATTY ACID PROFILE, DNA METHYLATION AND ADVERSE METABOLIC OUTCOMES IN THE OFFSPRING AT SCHOOL AGE Abel Lopez-Bermejo Received Received
  98-P3 A CASE OF CHILDHOOD TYPE 1 DIABETES MELLITUS WHO DEVELOPED GRANULOMA ANNULARE Havva Nur Kendirci Received Received
  98-P2 Use of Continuous Glucose Monitoring systems in the early detection and management of Cystic Fibrosis Related Diabetes in children Akinsola Ogundiya Received Received
  99-P1 Association of Serum Fibroblast Growth Factor 21 and Irisin with Insulin Sensitivity Markers and Serum Lipids in 12-year-old Children Satu Sepp Received Received
  99-P3 CASE REPORT: DE NOVO MUTATION OF FOXP3 CAUSING MILD PHENOTYPE OF IMMUNODYSREGULATION, POLYENDOCRINOPATHY, ENTEROPATHY, X-LINK SYNDROME HOANG THI DIEM THUY Received Received
  99-P2 Metabolic improvement offered by Medtronic Minimed 640 G associated to transient insulin perfusion suspension before hypoglycemia in young patients with type 1 diabetes. Ghada AL HAGE CHEHADE Received Received
  100-P1 Serum catestatin levels in obese children and adolescents Marko Simunovic Received Received
  100-P2 The glycemic variability in children with diabetes mellitus Oleg Dianov Received Received
  100-P3 Is there a relationship between Immune-mediated Type 1 Diabetes Mellitus and Congenital Rubella Infection? Huseyin Anil Korkmaz Received Received
  101-P3 Changes in Glycemic Control after switching from NPH & RI to Insulin Glargine & Lispro in Children with Type 1 Diabetes Mellitus(T1DM) Hyeon-A Kim Received Received
  101-P1 Circulating MOTS-c levels are decreased in obese male children and adolescents and associated with insulin resistance. Caiqi Du Received Received
  101-P2 The Levels of Blood Glucose And Counting of Carbohydrate-Fat-Protein In Diabetic Children Using Pump With Aspart And Glulisine emine demet akba&351; Received Received
  102-P2 A novel missense variant, p.(Thr405Arg), in the SLC19A2 gene in an infant with thiamine responsive megaloblastic anemia syndrome presenting with anemia and diabetes but with normal hearing Anita Spehar Uroic Received Received
  102-P3 WHEN TYPE MODY II DIABETES SIMULATES TYPE I DIABETES IRENE PILAR FERNANDEZ VISERAS Received Received
  102-P1 Plasma adropin levels are associated with lipid characteristics amongst children with obesity Ruimin Chen Received Received
  103-P3 EPIDEMIOLOGICAL STUDY AND ANALYSIS OF TYPE 1 DIABETES COMPARING PATIENTS WITH AND WITHOUT KETOACIDOSIS IN THE LAST 5 YEARS. IRENE PILAR FERNANDEZ VISERAS Received Received
  103-P2 Donohue syndrome With Hypertrophic Cardiomyopathy Derya Bulus Received Received
  104-P2 Age and exocrine pancreatic enzyme requirements are major determinants for carbohydrate metabolism impairment in children affected with cystic fibrosis Gabriel Á. Martos-Moreno Received Received
  105-P1 Effect of a Melanocortin-4 Receptor (MC4R) Agonist, Setmelanotide, on Obesity and Hyperphagia in Individuals Affected by Alstrm Syndrome Katie Fleming Received Received
  105-P3 MONOGENIC DIABETES CAUSE BY MUTATION OF THE GENE HNF1A Juan Manuel Narvaez Echeverri Received Received
  105-P2 Post-prandial hyperinsulinaemic hypoglycaemia after oesophageal surgery in children Antonia Dastamani Received Received
  106-P2 CONGENITAL HYPERINSULINISM: CLINICAL and MOLECULAR CHARACTERISTICS Fluorine-18-L-dihydroxyphenylalanine positron emission tomography (F-DOPA PET) SCAN RESULTS -TREATMENT RESPONSES AND SHORT TERM OUTCOMES OF 5 PATIENTS hande turan Received Received
  106-P3 REVERSIBILITY OF EARLY ACUTE DIABETIC NEUROPATHY (DN) IN ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS (T1D) Maria Louraki Received Received
  106-P1 Towards a greater understanding of the pathophysiology of obesity: hypothalamic obesity as a model of dysregulation of appetite and metabolic homeostasis Hoong-Wei Gan Received Received
  107-P1 Serum uric acid level and its association with metabolic syndrome in Korean adolescents So Yoon Jung Received Received
  107-P2 Congenital Hyperinsulinism in a child with Alagille Syndrome Antonia Dastamani Received Received
  108-P3 Psychosocial risks, comorbidities and health events during the follow-up of children and adolescents with type 1 diabetes M Carmen Temboury Received Received
  108-P1 More than a gut feeling: preliminary evidence supporting a role for lifestyle habits in shaping the intestinal microbiota in childhood and adolescence. Mélanie Henderson Received Received
  108-P2 Severe stress-induced insulin resistance in an eight year old boy with T1DM, reversed after psychiatric treatment Christi van Ommen Received Received
  109-P2 A case of neonatal diabetes due to pancreatic hypoplasia Zacharoula Karabouta Received Received
  109-P1 EFFICIENCY OF ALPHA-LIPOIC ACID IN METABOLIC SYNDROME TREATMENT IN CHILDREN Olena Tolstikova Received Received
  110-P3 Diabetes Mellitus, Autoimmune Hemolytic Anemia, Hepatosplenomegaly and Lymphadenopathy: a Rare Association in Chinese Children Miaoying Zhang Received Received
  110-P2 Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins Shira London Received Received
  110-P1 Lipid accumulation product is a predictor of non-alcoholic fatty liver disease in childhood obesity Bahar Ozcabi Received Received
  111-P1 Selected serum adipokines in children with irritable bowel syndrome Joanna Oswiecimska Received Received
  111-P3 Type 1 diabetes and central precocious puberty a rare association Mimouna Bessahraoui Received Received
  112-P2 A RARE CASE OF DIABETES MELLITUS TYPE 1 IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1 ELENI PANOUTSOU Received Received
  112-P1 Role of urinary NGAL and KIM-1 as early kidney injury biomarkers in obese prepubertal children Francesco Chiarelli Received Received
  112-P3 DIABETIC KETOACIDOSIS AMONG EGYPTIAN CHILDREN WITH TYPE 1 DIABETES: 3-YEARS STUDY Mona Karem Received Received
  113-P1 MATERNAL RESVERATROL INTAKE DURING PREGNANCY AND LACTATION MODULATES THE LONG-TERM METABOLIC EFFECTS OF MATERNAL NUTRITION ON OFFSPRING DEPENDING ON THE SEX AND DIET. PURIFICACIÓN ROS-PÉREZ Received Received
  113-P3 Fructosamine Level In Type 1 Diabetes Mellitus Children Performing Ramadhan Fasting nur rochmah Received Received
  114-P3 Metformin Therapy in A lean Adolescent girl with prediabetes dysglycemia treated: Good Response. ashraf soliman Received Received
  114-P2 Gender characteristics of responsibility for their own health of adolescents with type I diabetes mellitus Svitlana Chumak Received Received
  114-P1 Intrauterine metformin exposure and offspring metabolic health at 8-years follow-up Liv Guro Engen Hanem Received Received
  115-P3 Association Between Thyroid Stimulating Hormone and Hemoglobine A1c in Type 1 Diabetes Mellitus Children nur rochmah Received Received
  115-P1 Greater maternal BMI early in pregnancy and excessive gestational weight gain are independently associated with adverse health outcomes in the offspring at age 7 years Chiavaroli Valentina Received Received
  115-P2 Favorable outcome despite prolonged hypoglycemic episodes following a massive insulin overdose: a case series Heike Vollbach Received Received
  116-P1 Rapid BMI gain during later infant accelerates skeletal maturation at prepubertal obese children Toru Kikuchi Received Received
  116-P2 The Effect of a Reduced Fluid Replacement Regimen on the Resolution of DiabeticKetoacidosis (DKA) in Children Danica Shanee Hapuarachchi Received Received
  116-P3 Monogenic Diabetes in 2 Years and 4 Months Old Girl: Is it DEND? nur rochmah Received Received
  117-P3 Compliance for monitoring of glycemic control in children with type 1 diabetes Oleg Latyshev Received Received
  117-P2 Prevalence of and Risk Factors for Nonadherence to Insulin among Paediatric Type 1 Diabetes Patients in Singapore Brandon Chua Received Received
  117-P1 The more obese -the less pubertal height gain Anton Holmgren Received Received
  118-P1 LONGITUDINAL CHANGES IN ABDOMINAL FAT DISTRIBUTION IN THE FIRST TWO YEARS OF LIFE Inge van Beijsterveldt Received Received
  118-P3 Ketogenic Diet in a child with Diabetes and Global developmental delay Myat Win Received Received
  118-P2 What do you know about your diabetes?: a qualitative and quantitative study of teenagers and young adults understanding of their disease. Gianpaolo De Filippo Received Received
  119-P1 Telemedicine Therapy for Overweight Adolescents: First Results of a Novel Smartphone App Intervention using a Behavioural Health Platform Katrin Heldt Received Received
  119-P2 Parental Knowledge and Attitudes toward Diabetes Mellitus type 1: a cross sectional study Norah Albanyan Received Received
  120-P3 Oral Gliclazide (A Sulfonylurea) Monotherapy Is Effective and Safe in the Management of T2DM in Children, A Case Report. Ashraf Soliman Received Received
  120-P1 Cardiorespiratory fitness effectiveness is related to abdominal adiposity and insulin sensitivity in overweight adolescents Tetyana Chaychenko Received Received
  121-P3 Pediatric stroke as the presenting symptom of new onset diabetes without DKA Sonum Bharill Received Received
  121-P1 Promoting Healthy Lifestyles in Youth: Preliminary Findings from the CIRCUIT Program Marina Ybarra Received Received
  122-P1 Determinants of Attrition from a Healthy Lifestyle Intervention: Experience from the CIRCUIT Program Marina Ybarra Received Received
  122-P3 Challenges In Educating New Onset Type 1 Diabetes MellitusPatients: Can The Use Of a Tablet Be The Answer? Steven Ghanny Received Received
  122-P2 A Young Type 1 Diabetic with Acute Hemichorea: Rare central nervous system complications Andrew Sng Received Received
  123-P2 Allopurinol Ameliorates Non-alcoholic Fatty Liver Disease in Rats Huseyin Anil Korkmaz Received Received
  123-P3 AID-GM system (Advanced Intelligent Distant Glucose Monitoring) to monitor health status and metabolic control of young people with type 1 diabetes Valeria Calcaterra Received Received
  124-P2 Relationships of dietary intake and sugar rich products consumption with hepatic fat content and insulin resistance among children with overweight/obesity: The PREDIKID study Ignacio Diez Received Received
  124-P3 Continuous glucose monitoring results of our cases with MODY type 2 diabetes ZEYNEP UZAN TATLI Received Received
  125-P3 NKX2-2 human mutation causes neonatal diabetes followed by severe infantile obesity associated with paradoxical upregulated ghrelin levels do beta-cells secrete ghrelin? Adi Auerbach Received Received
  125-P2 Angiotensin- Converting Enzyme Insertion/Deletion Gene Polymorphism in Egyptian Obese Children and Adolescents: Relation to Hypertension Risk Rasha Hamza Received Received
  126-P2 Serum calprotectin level in children: marker of obesity and its metabolic complications. Valeria Calcaterra Received Received
  126-P1 Effect of hormonal changes on exocrine pancreatic function in girls with anorexia nervosa Ma&322;gorzata Stojewska Received Received
  126-P3 Tracing the Effect of the Melanocortin-4 Receptor Pathway in Obesity: Study Design and Methodology of the TEMPO Registry Katie Fleming Received Received
  127-P3 BigO: Big Data Against Childhood Obesity Anastasios Delopoulos Received Received
  127-P1 PCSK9 and Lp(a) levels of children born after ?ssisted Reproduction Technologies Ioanna Kosteria Received Received
  127-P2 Pediatric Continuous Metabolic Syndrome Score (PsiMS score): Use in Everyday Clinical Practice Rade Vukovic Received Received
  128-P2 LEPTIN AND CYTOKINES ARE NOT THE BEST MARKERS FOR METABOLIC S. Beatriz Garcia Cuartero Received Received
  128-P3 Exposure to bisphenol-A and phtalates in obese girls annalisa deodati Received Received
  128-P1 Rate of accumulation of abdominal fat is associated with fasting glucose levels in early childhood Suresh Anand Sadananthan Received Received
  129-P1 Early menarche is associated with insulin resistance and non-alcoholic fatty liver disease in obese adolescents ANNA DI SESSA Received Received
  129-P2 Early-life risk factors and their association with hypertension in Spanish children and adolescents Gloria Bueno-Lozano Received Received
  129-P3 OBESITY OF CHILDHOOD and AMBULATORY GLUCOSE MONITORIZATION Aya Trel Ergr Received Received
  130-P2 A rare case of diabetes mellitus in an adolescent: partial lipodystrophy Samim zen Received Received
  130-P3 Familial Partial Lipodystrophy, Importance of family history - a case report Camilla Stockley Received Received
  130-P1 The frequency of obstructive sleep apnea in children with hypothalamic and exogenous obesity DICLE CANORUC Received Received
  131-P2 Visfatin, RBP4 and STRA6 polymorphisms in relation with childhood obesity Ionela Pascanu Received Received
  131-P3 Development of severe obesity in a child with a brainstem tumor Catherine Pihoker Received Received
  131-P1 THE IMPORTANCE OF UNIVERSAL LIPID PROFILE SCREENING IN TWO TO TEN YEARS OLD LEBANESE CHILDREN. Georges Nicolas Received Received
  132-P1 Non-invasive measurements of central blood pressure with arterial stiffness indicators as a new research tool for predicting cardiovascular risk in children with type 1 diabetes mellitus and obesity Klaudyna Noiszewska Received Received
  132-P2 CHARACTERISTICS OF BLOOD LIPIDS IN BOYS WITH HYPOANDROGENIA Olena Budreiko Received Received
  132-P3 CORRELATION BETWEEN OBESITY, BODY MASS INDEX AND INSULIN RESISTANCE IN BULGARIAN CHILDREN Desislava Yordanova Received Received
  133-P3 Nonclassical manifestation of PWS Elena Bogova Received Received
  133-P2 Tri-Ponderal Mass Index. A good anthropometric index to evaluate adiposity in children and adolescents. Miguel Klnder Received Received
  133-P1 Severe Obesity and Cardiometabolic Comorbidities in Adolescents: Chronology of an Epidemic Orit Pinhas-Hamiel Received Received
  134-P3 Metabolic parameters in children with syndromic obesity Elena Sukarova-Angelovska Received Received
  134-P2 Serum Spexin Concentrations in Adolescent Females with Metabolic Syndrome, Polycystic Ovary Syndrome and Anorexia Nervosa FLORA BACOPOULOU Received Received
  134-P1 Evaluation of intraocular pressure and retinal nerve fiber layer, retinal ganglion cell, central macular thickness and choroidal thickness using optical coherence tomography in obese children and healthy controls R&305;za Taner Baran Received Received
  135-P1 Cardiac and Vascular Assessments in Small- versus Appropriate-for-Gestational-Age Infants at Ages 1 and 2 Years Cristina Garcia-Beltran Received Received
  135-P3 Cut-off for the follow-up of obese children: cynicism or realism? Francesco Gallo Received Received
  135-P2 A SIMPLE RELAXATION EXERCISE REDUCES STRESS IN OBESE YOUTH - A PATH TO A HEALTHY LIFESTYLE? Aikaterini Stasinaki Received Received
  136-P2 Dyslipidemia and Its Related Factors in Chinese Children and Adolescents with Turner Syndrome Siqi Huang Received Received
  136-P3 PROXIMAL MICRODELECTION 16p11.2 SYNDROME Francesco Leo Received Received
  136-P1 BONE MATURATION AS A PREDICTIVE FACTOR OF CATCH-UP GROWTH DURING THE FIRST YEAR OF LIFE IN BORN SMALL FOR GESTATIONAL AGE INFANTS: A PROSPECTIVE STUDY Giorgia Pepe Received Received
  137-P2 Severity, duration and phenotype of obesity promote precocious cardiovascular sonographic alterations in childhood obesity. Domenico Corica Received Received
  137-P1 NEONATAL SCREENING TESTS IN PREMATURE NEWBORNS IN SOUTHERN BRASIL Suzana Nesi-Frana Received Received
  138-P2 Physical activity determined by accelerometry before and after an integral treatment program in children with abdominal obesity María Cristina Azcona Received Received
  138-P1 Measurement of estradiol and testosterone in umbilical cord blood by gas chromatography-tandem mass spectrometry (GC-MS/MS); comparisons with radioimmunoassay (RIA) Kerstin Allvin Received Received
  138-P3 A compound heterozygote mutation in a Chinese patient affected with Methylmalonic acidemia HUI HUANG Received Received
  139-P1 Transient neonatal iatrogenic hypothyroidism due to iodinated contrast Ulrika Hrenstam Received Received
  139-P3 LYMPOSOMAL ACID LIPASE DEFICIT IN PATIENTS WITH HYPERCHOLESTEROLEMIA Ignacio Diez Received Received
  140-P3 HEPATIC STEATOSIS AND ITS RELATIONSHIP WITH THE METABOLIC SYNDROME IRENE PILAR FERNANDEZ VISERAS Received Received
  140-P1 SEXUAL DIMORPHISM OF IGF1 AND IGF2 EXPRESSION IN THE NEONATAL RAT BRAIN Julie Chowen Received Received
  140-P2 Sex-related differences and effect of puberty on Metabolic Syndrome in obese children and adolescents Chiara Guzzetti Received Received
  141-P1 Autosomal Dominant Growth Hormone Deficiency due to a novel c.178GA mutation in the GH1 gene causing instability of the mutant GH protein (p.Ala34Thr). Bradley Miller Received Received
  141-P3 Serum hepcidin and ferritin in prepubertal obese children Joanna Gajewska Received Received
  141-P2 Associations between total leptin, bio-inactive leptin, soluble leptin receptor and anthropometrics in children with severe early-onset obesity (SEOO) the German-Polish Study (EOL-GPS) Agnieszka Zachurzok Received Received
  142-P3 Osse Registry for Patients with Lipodystrophy run by the European Consortium of Lipodystrophy (ECLip) Julia von Schnurbein Received Received
  142-P2 Children with obesity are taller in early childhood with subsequent catch-down growth until adolescence Elena Kempf Received Received
  142-P1 GROWTH HORMONE DEFICIENCY DUE TO WHOLE-GENE DELETION OF GHRHR Sezer Acar Received Received
  143-P1 Severe pre- and postnatal growth retardation in a child harboring a novel homozygous IGF1 gene mutation. Ana Claudia Keselman Received Received
  143-P3 Acanthosis nigricans in obese children and adolescents in relation to severity of obesity and insulin resistance. Kyung Hee Park Received Received
  143-P2 The relationship between anthropometric measurements and breast milk ghrelin and nesfatin-1 levels in infants with small for gestational age Berna Filibeli Received Received
  144-P3 Serum uric acid and its correlation with metabolic syndrome factors in simple obesity children ZULIN LIU Received Received
  144-P2 Efficacy, safety and tolerability of Liraglutide, GLP-1 Analogue, in Indian adolescent population with obesity Inderpal Kochar Received Received
  145-P2 THE EFFECT OF EXCLUSIVE BREASTFEEDING AND FORMULA FEEDING ON BODY COMPOSITION DURING THE FIRST TWO YEARS OF LIFE Kirsten Sabine de Fluiter Received Received
  145-P3 Thyroid function, lipid profile and carbohydrate metabolism parameters in patients with Alstrom syndrome. Maja Oko&324;ska Received Received
  145-P1 Response to growth hormone in patients with isolated familial growth hormone deficiency due to RNPC3 mutations Gabriel Á. Martos-Moreno Received Received
  146-P2 Body composition and cardiovascular function in pre-adolescent children of South Asian and White European origin: Relationship to maternal status in pregnancy. Andrew Whatmore Received Received
  146-P3 Does the level of studies of parents influence the follow-up of the recommendations of the nutritional pyramid? María Rosaura Leis Trabazo Received Received
  146-P1 Laron syndrome patients have an abnormal plasma amino acid pattern Laron Zvi Received Received
  147-P3 Bariatric surgery as treatment of primary Pseudotumor cerebri in a male adolescent: case report Marina Ybarra Received Received
  147-P2 Relation between cardiac function and anthropometric parameters in overweight and obese school boys Viktoriya Furdela Received Received
  147-P1 Serum IGFBP-2 concentration in neonates with potential diagnosis of growth hormone deficiency (GHD). MARIA GABRIELA BALLERINI Received Received
  148-P3 Investigation of Pubertal Effect on Thyroid Volume and IGF-1 Changes in Morbid Obese Children Murat Karaoglan Received Received
  148-P2 EVALUATION OF HYDRATION STATUS OF OBESE CHILDREN- A PILOT STUDY Ayse Nurcan Cebeci Received Received
  149-P2 GALANIN IS POSITIVELY CORRELATED WITH INSULIN RESISTANCE AND TRIGLYCERIDE LEVELS IN OBESE CHILDREN Sezer Acar Received Received
  149-P3 The effect of vitamin D supplementation on metabolic syndrome parameters in overweight and obese children and adolescents in Greece Christos Giannios Received Received
  149-P1 Assesment of SDF-1 and Ang-1 and Ang-2 in children with growth hormone deficiency before and after 1- year therapy with recombinant growth hormone Beata Sawicka Received Received
  150-P3 Mothers obesity and high childs waist circumference are predictive factors of severe childs obesity: an Observational Study in French Guiana Njuieyon Falucar Received Received
  150-P2 Brown Adipose Tissue in Prepubertal Children: Association with Sex and with the Sequence of Prenatal Growth Restraint and Postnatal Catch-Up Rita Malpique Received Received
  150-P1 Total Sum of Growth Hormone Values obtained from Growth Hormone Stimulation Test may be useful in the Diagnosis of Prepubertal Children with Idiopathic Growth Hormone Deficiency. Su-Jeong Lee Received Received
  151-P3 LIPIDOGRAM, LEPTIN-AND ADIPONECTINAEMIA IN TEENAGERS AND ADOLESCENTS WITH METABOLIC SYNDROM Olena Tolstikova Received Received
  152-P3 Metabolic Endotoxemia in Egyptian Obese Children And Adolescents Omneya Omar Received Received
  152-P2 Does Late Sleeping Time Results Increased Bedtime Snack? What Is The Risk Of This In Childhood Obesity? mehmet mustafa y&305;lmaz Received Received
  152-P1 MICROALBUMINURIA AND GLOMERULAR FILTRATION RATE IN SGA BORN YOUNG ADULTS Wesley Goedegebuure Received Received
  153-P2 Early BMI Trajectory Classes are Linked to Distinct Body Fat Partitioning Later in Childhood Navin Michael Received Received
  153-P3 Resting metabolic rate and the development of metabolic disorders in obese children Pavel Okorokov Received Received
  153-P1 Testing the performance of a preexisting growth prediction model in a cohort of prepubertal patients born small for gestational age (SGA) receiving GH treatment in PATRO children. Christof Land Received Received
  154-P1 Early onset GH replacement in GH deficiency: Is neonatal hypoglycemia important for long term follow-up? Dicle EMET Received Received
  154-P2 Hair Cortisol Concentrations in Overweight and Obese Children and Adolescents Sofia Genitsaridi Received Received
  154-P3 Relation Of Screen-Time(Phone-Computer-TV-Online Games) And Physical Activity With Childhood Obesity Mehmet mustafa YILMAZ Received Received
  155-P2 Associations between body fat mass and internalizing and externalizing behaviors and anxiety in children and adolescents Eirini Christaki Received Received
  155-P3 Effect of three-month diet and physical activity on adipokines and inflammatory status in children with metabolic syndrome Ramona Stroescu Received Received
  155-P1 Prevalence of diabetes among children treated with growth hormone in Israel Zvi Laron Received Received
  156-P2 Pharmacotherapy and the effects on LDL levels and growth in 2 children with severe Familial Hypercholesterolemia Aravind Venkatesh Sreedharan Received Received
  156-P3 NECK CIRCUMFERENCE AND LIPID PROFILE IN ADOLESCENTS WITH OVERWEIGHT / OBESITY Ricardo Arrais Received Received
  156-P1 The effect of growth hormone treatment in children after hematopoietic stem cell transplantation Sabine Hannema Received Received
  157-P3 A not so simple obesity Silvia Poluzzi Received Received
  157-P1 Easypod Connect Observational Study: The Italian Experience Giovanna Orlando Received Received
  157-P2 Brown tumors in children on hemodialysis russka shumnalieva Received Received
  158-P1 Patients and caregivers perspectives on a mobile app that tracks adherence and outcomes in children with growth disorders treated with recombinant human growth hormone (r-hGH) Mel West Received Received
  158-P2 The role of fibroblast growth factor 21 and irisin in the pathogenesis of obesity in childhood and adolescence Sofia-Iliada Karampatsou Received Received
  159-P1 Does X-chromosome gene dosage determine growth and phenotypic features in Turner syndrome with 45,X/46,XX mosaicism on standard karyotyping? A cross-sectional analysis of the French national rare disease network database Elodie Fiot Received Received
  159-P2 Serum NAMPT levels are not associated with parameters of liver function in children and adolescents Antje Garten Received Received
  159-P3 COMPLIANCE OF OBESE CHILDREN AND THEIR FAMILY TO THE DIRECTIONS OF A PEDIATRIC ENDOCRINOLOGY MEDICAL OFFICE Sotiria Giannopoulou Received Received
  160-P3 RISK FACTORS AND COMORBIDITIES OF CHILDHOOD OBESITY Sotiria Giannopoulou Received Received
  160-P2 Obesogenic environment and its influence on adiposity on Mexican children and adolescents. América Miranda_Lora Received Received
  161-P3 AUTONOMIC NERVOUS SYSTEM -INFLAMMATION LINK: A NEW INDEPENDENT MECHANISM FOR HOMEOSTASIS STYLIANI GERONIKOLOU Received Received
  161-P2 Metabolic alterations and weight status in children at 8 years: a prospective cohort study ISOLINA RIAÑO-GALAN Received Received
  162-P1 Comparing the cumulative dose of growth hormone therapy using body weight-based dosing versus body surface area-based dosing in children with Turner syndromedata from the ANSWER study Philippe Backeljauw Received Received
  162-P2 Correlation of dietary habits with systolic blood pressure in healthy children Maria Efthymia Katsa Received Received
  162-P3 Effects of a brief Physician delivered counseling on childhood obesity SUNETRA MONDAL Received Received
  163-P2 Evaluation of voiding dysfunction in obese children bayram ozhan Received Received
  163-P1 The Association between Growth Hormone Dose and Short-Term Height Outcomes in a Large Cohort of Paediatric Patients with Turner Syndrome: Real-World Data from the NordiNet International Outcome Study (IOS) and the ANSWER Program Jo Blair Received Received
  164-P1 Changing patterns of growth in Prader-Willi syndrome Georgia Irene Neophytou Received Received
  164-P2 Comparison of antropometric and biochemical parameters in obese children with or without primary headache onur AKIN Received Received
  165-P2 The protective effect of exclusive breastfeeding for overweight/ obesity in children with high birth weight Hae Soon Kim Received Received
  166-P2 Determinants and consequences of exaggerated adrenarche in simple obesity. Jean De Schepper Received Received
  166-P1 SAFETY AND EFFECTIVENESS OF GROWTH HORMONE TREATMENT IN PATIENTS WITH PRADER-WILLI SYNDROME UNDER 2 YEARS OF AGE IN A REFERENCE HOSPITAL Raquel Corripio Received Received
  166-P3 Assessment of obesity in children with achondroplasia and hypochondroplasia Yukako Nakano Received Received
  167-P1 Improved mental and motor development during 3 years of GH treatment in very young children with Prader-Willi syndrome Stephany Donze Received Received
  167-P3 Correlation of lipoprotein(a) levels and family history of cardiovascular disease in a sample of overweight/obese children and adolescents Zacharoula Karabouta Received Received
  167-P2 Metabolic alteration in Patients affected by PseudoHypoParathyroidismo 1a (PHP1a): a preliminary data Danilo Fintini Received Received
  168-P2 Weight loss outcomes in two-year multidisciplinary lifestyle intervention program involving obese children and their parents Katja Dumic Kubat Received Received
  168-P1 GH response to GHRH and Arginine in previously GH-treated young adults with Prader-Willi syndrome Stephany Donze Received Received
  168-P3 Beneficial effect of metformin treatment in obese children and adolescents Zdravka Todorova Received Received
  169-P1 A novel type of Pubertal Height, Weight, and BMI Reference, aligned for Onset of Puberty. Anton Holmgren Received Received
  169-P2 Relationship between glucose and lipid metabolism, inflammatory factors and adipokines in children with obesity Ruimin Chen Received Received
  170-P1 Evaluating cut-offs for automatic growth screening in Swedish children using the Finnish growth monitoring algorithm Lars Gelander Received Received
  170-P2 Development of resistance to Sorafenib, a multikinase inhibitor, in hepatocellular carcinoma is mediated by SIRT Antje Garten Received Received
  171-P2 GENDER AND PUBERTAL TENDENCIES OF PLASMA LEPTIN AND DOPAMINE LEVELS DEPENDING ON TAQIA DRD2 GENE POLYMORPHISM IN THE DIFFERENT PEDIATRIC OBESITY CLASSES. Liudmila Viazava Received Received
  171-P3 COMPARISON OF METABOLIC PARAMETERS OF OFFSPRINGS BLOOD DEPENDING ON THE LEVEL OF GLYCEMIA DURING PREGNANCY Alisa Masel Received Received
  171-P1 Prospective study of growth in Swedish children treated with modified ketogenic diet Anna Svedlund Received Received
  172-P2 Iron metabolism disorders in prepubertal obese children with and without NAFLD Francesco Chiarelli Received Received
  172-P1 Early Gut Mycobiota and Childhood Growth Kasper Schei Received Received
  172-P3 Forty patients with persistent, non-focal congenital hyperinsulinism: Urgent need for new treatment modalities Amalie Greve Rasmussen Received Received
  173-P3 Outcome of eight patients with congenital hyperinsulinism (CHI) studied with 18FDihydroxyphenyl-Alanine Positron Emission Tomography Imaging (18F-DOPA-PET-CT) in Argentina ANA TANGARI SAREDO Received Received
  173-P2 Familial hypercholesterolemia due to homozygous LDLRAP1 mutation: variability of phenotype and response to medical therapy. Evangelia Panou Received Received
  173-P1 Clinical and radiological manifestations in a large Swedish family with a pathogenic heterozygous ACAN variant Alexandra Gkourogianni Received Received
  174-P2 CAN TRIPONDERAL MASS INDEX BE A NEW INDICATOR IN THE PREDICTING CARDIOMETABOLIC RISK IN OBESE ADOLESCENTS? Berna Filibeli Received Received
  174-P1 IDENTIFICATION OF ADAMTS6 AS A NOVEL CANDIDATE GENE FOR IDIOPATHIC SHORT STATURE WITH ADVANCED BONE MATURATION Diana Monica Warman Received Received
  175-P2 Social Networks, Social Support and Weight-Related Outcomes among Adolescents Marina Ybarra Received Received
  175-P3 NEONATAL DIABETES MELLITUS IN VIETNAM NATIONAL CHILDREN HOSPITAL Ngoc Can Thi Bich Received Received
  175-P1 Dual function of the retinoic acid catabolizing enzyme CYP26C1 underlying idiopathic short stature and modifying disease severity in SHOX deficiency Gudrun Rappold Received Received
  176-P1 Growth plate disorders are the main cause of severe familiar short stature in children classified and treated with growth hormone as SGA or GHD Luká Plach Received Received
  176-P3 AXILLARY TEMPERATURE RELATION TO BLOOD SERUM INSULIN-LIKE GROWTH FACTOR-I IN THE NOT-LIFE-THREATENED NEWBORN: RELEVANCE OF PRETERM BIRTH Cesare Terzi Received Received
  176-P2 Identification of A Novel Homozygous Mutation in BBS10 in Five Children With Bardet-Biedl Syndrome glay can y&305;lmaz Received Received
  177-P2 THE EFFECTS OF THE BIRTH WEIGHT ON THE FAT DISTRIBUTION AND FATNESS PARAMETERS OF THE BODY GUL D&304;REK Received Received
  177-P3 BIRTH ESTIMATED BRAIN WEIGHT RELATION TO RATIOS BETWEEN INSULIN-LIKE GROWTH FACTOR-II AND INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN-3 IN THE NOT-LIFE-THREATENED NEWBORN: RELEVANCE OF AXILLARY TEMPERATURE Cesare Terzi Received Received
  177-P1 Genetic investigation of children with syndromic prenatal onset short stature THAIS HOMMA Received Received
  178-P3 Congenital Hyperinsulinism in Children with Beckwith-Wiedemann syndrome Diliara Gubaeva Received Received
  178-P2 Oxidative homeostasis dysregulation may promote pathogenesis of cardio-metabolic complications in childhood obesity Domenico Corica Received Received
  178-P1 : Identification of three novel mutations in 10 pediatric patients with unexplained syndromic short stature identified by targeted exome sequencing in Korea CHONG KUN CHEON Received Received
  179-P3 Comparison of the phenylketonuria phenotypes in Qazvin province before and after neonatal screening until 2017 Fatemeh Saffari Received Received
  179-P1 Beckwith Wiedemann syndrome: first international consensus regarding diagnosis and clinical management. FREDERIC BRIOUDE Received Received
  179-P2 Body composition parameters, systemic inflammation and metabolic syndrome manifestations in children and adolescents Eirini Christaki Received Received
  180-P1 Silver Russell and Beckwith-Wiedemann syndromes: Mosaic distribution of epigenetic anomalies PHAM Aurélie Received Received
  180-P2 Relationships between Obesity Parameters and Urinary Concentrations of Phthalates and Phenols in Korean Girls Mi-Jung Park Received Received
  180-P3 From Hypoglycemia to Hyperglycemia Ho-chung YAU Received Received
  181-P3 Population screening of hypophosphatasia. A metabolopathy to consider.National multicentric study Ignacio Diez Received Received
  181-P2 Clinical characteristics of congenital hyperinsulinism caused by dominant KCNJ11/ABCC8 mutations. Maria Melikyan Received Received
  181-P1 Long term effects of childhood growth hormone treatment on height and body mass index in adolescents and adults with Silver-Russell syndrome. Oluwakemi Lokulo-Sodipe Received Received
  182-P2 Clinical characterstics, genotype-phenotype correlations and follow up of patients with congenital hyperinsulinaemic hypoglycaemia; single center experience from a southeastern city of Turkey Huseyin Demirbilek Received Received
  182-P1 Year-one Effectiveness and Overall Safety of NutropinAq for Growth Hormone Deficiency (GHD) and Other Paediatric Growth Disorders: Completion of the International Cooperative Growth Study (iNCGS) European Registry Regis Coutant Received Received
  182-P3 Dumping Syndrome in a neonate with Esophageal Atresia Surgery Jennyfer Monroy Espejo Received Received
  183-P2 CONGENITAL HYPERINSULINISM: MANAGEMENT & OUTCOME IN WEST OF SCOTLAND Khadiga Eltonbary Received Received
  183-P1 Carriers of IGF1-receptor mutations as a subgroup of SGA patients: a comprehensive retrospective comparison of response to rhGH treatment and health profile Eric Gpel Received Received
  183-P3 Diagnosis and treatment of persistent hyperkalemia in newborn twins ----Rare case report of Gordon syndrome jun zhang Received Received
  184-P3 MUTATION IN UCP2 GENE: A RARE CAUSE OF HYPERINSULINEMIC HYPOGLYCAEMIA SYNDROME IN A SMALL-FOR-GESTATIONAL AGE NEWBORN Pamela Yesquen Salcedo Received Received
  184-P1 Characteristics, effectiveness and safety data for patients with growth failure treated with recombinant IGF-I and achieving adult or near-adult height: results from the European Increlex Growth Forum Database registry Michel Polak Received Received
  184-P2 20 cases of congenital hyperinsulinism in Ukraine Evgenia Globa Received Received
  185-P3 HYPERINSULINEMIC HYPOGLYCAEMIA SYNDROME IN SMALL-FOR-GESTATIONAL AGE NEWBORNS: CLINICAL CHARACTERISTICS AND GENETIC STUDY Pamela Yesquen Salcedo Received Received
  185-P2 Nifedipine therapy in hyperinsulinaemic hypoglycaemia due to mutations in the PMM2 gene improves fast tolerance, stabilises blood glucose profile, and enables rationalisation of treatments for glycaemic control and hypertension: the first reported trial i Harshini Katugampola Received Received
  186-P2 Potentially modifiable predictors of adverse neonatal outcomes in women with gestational diabetes mellitus (GDM). Maria-Christina Antoniou Received Received
  186-P1 Maternal uniparental disomy for chromosome 20: physical and endocrinological characteristics of six patients Sayaka Kawashima Received Received
  186-P3 Pediatric insulinoma: A case report Pathikan Dissaneevate Received Received
  187-P1 A novel deadly variant in the TP53 gene causing Li-Fraumeni Syndrome. The importance of clinical awareness and the contribution of molecular diagnosis in active prevention within families with multiple tumor incidents at a young age. Christina Bothou Received Received
  187-P2 A boy with diazoxide unresponsive congenital hyperinsulinism due to a homozygous ABCC8 missense mutation previously reported to be dominant Sonya Galcheva Received Received
  188-P2 Diazoxide unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation. YASMINE OUAREZKI Received Received
  188-P1 Mutations in SHOX, GHR and IGFALS genes among Indian children with idiopathic short stature Vandana Jain Received Received
  188-P3 Weight outcome ininfants with prolonged hyperinsulinemic hypoglycemia treated with Diazoxide versus those with spontaneous resolution SURESH CHANDRAN Received Received
  189-P3 Neonatal hyper- and hypoglycaemia; widening the clinical phenotype of transient neonatal diabetes mellitus due to 6q24 methylation defects. Tashunka Taylor-Miller Received Received
  189-P1 Clinical features and assessment of the pathway-care proposed by ISPED-Gsa Study Group in an Pediatric Italian cohort with Pseudohypoparathyroidism Luisa de Sanctis Received Received
  189-P2 Neonatal hypoglycaemia: unchanged risk of neurodevelopmental impairment, but sex-specific decreased fine motor function and increased internalizing behaviour at school age Annett Helleskov Received Received
  190-P1 Overview of leading causes of death among French patients with Prader-Willi Syndrome, 2004-2014 Dibia Liz Pacoricona Alfaro Received Received
  190-P2 Hepatoblastoma and Wilms Tumour in an infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism SAURABH UPPAL Received Received
  191-P3 Transient Central Hypothyroidism due to Maternal Graves disease YUKIE IZUMITA Received Received
  191-P2 Association between Rubenstein-Taybi Syndrome and hyperinsulinaemic hypoglycaemia Ranna El-Khairi Received Received
  192-P3 Good Growth Response to Growth Hormone Therapy in Short Children with Normal Growth Hormone Secretion AHMED EL AWWA Received Received
  192-P2 Hyperinsulinemic hypoglycemia in congenital disorder of glycosylation type-1a (CDG-1a) Dogus Vuralli Received Received
  192-P1 Final adult height, Insulin-like Growth Factor 1 (IGF-I) concentration in adolescents and young adults with -thalassemia major (BTM) with and without Growth hormone Deficiency Ashraf Soliman Received Received
  193-P2 A rare cause of hyperinsulinemic hypoglycemia: Costello syndrome Dogus Vuralli Received Received
  193-P1 McCune-Albright-Syndrome: clinical and genetic study in a large cohort of pediatric patients. Nadezhda Makazan Received Received
  194-P3 Growth hormone treatment: does timing matter? Bernardo Marques Received Received
  194-P1 A 7-year update report of a national, interdisciplinary endeavour to improve outcomes for children and young people under 19years of age with Hypothalamic Pituitary Axis Tumours (HPAT) using multi-site video conferencing Katja Freund Received Received
  195-P2 THE BENEFIT OF UNIVERSAL NEONATAL SCREENING FOR HYPOGLYCEMIA Georges Nicolas Received Received
  195-P1 Long Term Reversibility of Presumed ACTH Deficiency (ACTHd) in Children and Young People (CYP) with Intracranial Germ Cell Tumours (IGCT). KYRIAKI PIERI Received Received
  195-P3 Support for patients treated with growth hormone to reach their growth potential: addressing adherence barriers through personalised behavioural patient-support programmes Melanie West Received Received
  196-P1 Endocrine follow-up of children with a history of brain tumour. Data from our large cohort at Necker University Hospital, Paris, 2010-2015. Laura Gabriela González Briceño Received Received
  196-P2 Prematurity of 23 or less weeks gestation is a risk for transient late-onset hyperglycemia in neonates Takeru Yamauchi Received Received
  196-P3 Main discrepancies between predicted and observed growth responses with iGRO in children treated with GHr in Spain Cristina Mora Palma Received Received
  197-P1 A single centre experience of managing a series of childhood macro/giant-prolactinoma Antonia Dastamani Received Received
  197-P2 An unusual cause of neonatal hyperglycemia case report Joana Matos Received Received
  197-P3 Adherence and long-term outcomes of therapy in pediatric subjects in Greece using easypod electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod Connect Observational Study (ECOS) Melanie West Received Received
  198-P3 Growth hormone deficiency in neurofibromatosis: report of four cases Elisa Guidoni Received Received
  198-P1 A national UK guideline for managing pituitary adenomas in children and young people under 19 years developed according to the AGREE II framework Joanne Blair Received Received
  198-P2 NEONATAL HYPOCALCEMIA DUE TO MATERNAL HYPOVITAMINOSIS D: A COHORT OF CHILDREN IN A REGION OF NORTHERN SPAIN maria laura Bertholt Received Received
  199-P2 Evaluation of vitamin D status and its correlation with gonadal function in children at mini-puberty Suna KILIN Received Received
  199-P3 EXTREMELY LOW BODY MASS INDEX NEGATIVELY IMPACT THE RESPONSE TO GROWTH HORMONE TREATMENT IN CHILDREN WITH GROWTH HORMONE DEFICIENCY Irina Delia Nicolaescu Received Received
  200-P3 Small for gestational age patients with premature treatment discontinuation: their journey in French, real-life settings Jean-Pierre Salles Received Received
  200-P2 Systemic pseudohypoaldosteronism type 1 due to 3 novel mutations in SCNN1A and SCNN1B genes; report of 3 cases Atilla Cayir Received Received
  200-P1 PROKR2 Mutations in Patients with Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency Asl&305; Derya Kardelen Received Received
  201-P1 Anastrozole is safe as monotherapy in early maturing girls with compromised growth, further improving gain in predicted adult height by the initial combination therapy of an LHRH analogue and an aromatase inhibitor. Results from the GAIL study ISRCTN114 Eleni Dermitzaki Received Received
  201-P3 Effects on Near-Adult Height and Safety of Recombinant Human Growth Hormone in Patients with Growth Hormone Deficiency and Turner Syndrome: Results from the LG Growth Study Jong Hee Jin Received Received
  201-P2 Postnatal Growth of Infants with Neonatal Diabetes: Insulin pump (CSII) versus Multiple Daily Injection (MDI) therapy ashraf soliman Received Received
  202-P2 Serum vaspin concentration in full-term, appropriate-for-gestational-age newborns: effect of early-onset infections Ma&322;gorzata Stojewska Received Received
  202-P1 Long acting octreotide treatment in children with growth hormone excess and neurofibromatosis type 1-optic pathway tumors Paula Ximena Molina Giraldo Received Received
  202-P3 Final adult height after growth hormone treatment in patients with Turner syndrome Jungmin Ahn Received Received
  203-P1 Serum concentrations of the endocrine disruptors-organochlorine pesticides (OCPs) in Greek children with Neurodevelopmental Disorders Gerasimos Makris Received Received
  203-P3 Results of mecasermin treatment in pediatric patients evaluated for severe and partial primary deficiency of IGF-1 Karolina Stozek Received Received
  203-P2 First Three Years of the Congenital Adrenal Hyperplasia Neonatal Screening Program of the State of Parana, Southern Brazil GABRIELA DE CARVALHO KRAEMER Received Received
  204-P2 Assessment of the stretched penile length in Sri Lankan newborns Dona Udeni Anuruddhika Kollurage Received Received
  204-P3 Children born small for gestational age treated with growth hormone: evolutionary aspects. Verónica María Padín Vázquez Received Received
  205-P2 Auxological catch up growth and evaluation of spontaneous motility in the term newborn Small for Gestational Age employing the Prechtl assessment of General Movements. Laura Lucaccioni Received Received
  205-P1 A paternally inherited familial precocious puberty caused by a novel MKRN3 frameshift variant Jessica Odone Received Received
  205-P3 Small for gestational age patients in real-life, French clinical practice: what is the difference between good and poor responders to growth hormone treatment? Marc Nicolino Received Received
  206-P1 MKRN3 levels in girls with central precocious puberty during GnRHa treatment: a longitudinal study anna grandone Received Received
  206-P3 Body Mass Index (BMI) in patients with Growth Hormone Deficiency (GHD) at diagnosis, one year and two years after treatment with Growth Hormone (GH) Maria Claudia Schmitt-Lobe Received Received
  206-P2 Identification of three novel GLI2 gene variants associated with Hypopituitarism Lidia Castro-Feijoo Received Received
  207-P2 Clinical and preliminary molecular description of a cohort of patients with growth retardation due to severe primary IGF1 deficiency (GROWPATI study) ATHANASIA STOUPA Received Received
  207-P3 Erythropoietin and Granulocyte Macrophage Colony Stimulating Factor levels in Growth Hormone Deficient Children after 1 Year of Growth Hormone Therapy Maria Pankratova Received Received
  208-P3 Cost-effectiveness of growth hormone therapy in children in Russia Maria Vorontsova Received Received
  208-P1 Testicular Development And Puberty In Boys With Duchenne Muscular Dystrophy: Results From The ScOT-DMD Study Melissa Denker Received Received
  208-P2 A Novel, Synonymous, Heterozygous, Splicing Variant Affecting the Intracellular Domain of the Growth Hormone Receptor: Causality for Mild Growth Impairment and IGF-I deficiency in an Affected Patient? DIONYSIOS CHRYSIS Received Received
  209-P1 Exposure to BPA and phthalates and timing of puberty in girls annalisa deodati Received Received
  209-P2 A novel mutation of type I insulin-like growth factor receptor (IGF1R) gene in a severe short stature pedigree identified by targeted Next-generation sequencing (NGS) HUI HUANG Received Received
  209-P3 Vitamin D status in children with isolated idiopathic Growth hormone deficiency (GHD) in North and Central Greece Maria Xatzipsalti Received Received
  210-P1 Hypothalamic-pituitary-testicular axis response to sub-maximal aerobic exercise, in pre- and early- pubertal normal weight and obese boys. George Paltoglou Received Received
  210-P2 Severe short stature, Growth Hormone (GH) Deficiency, Hypospadias, and Microcephaly: New Insights into the Role of Chromosome 4 Long Arm Duplication Basma Haris Received Received
  210-P3 A pilot study for comparing efficacy and safety of the CinnaTropin to the reference recombinant human growth hormone in children with isolated growth hormone deficiency and multiple pituitary hormone deficiency Maryam Razzaghy-Azar Received Received
  211-P1 Effect of pubertal blockade and cross-sex hormone treatment on the growth spurt in young transgender adolescents: a first report. Gary Butler Received Received
  211-P3 Study of the effectiveness of growth hormone in children born small for gestational age in an area of ??northwestern Spain and its associated factors Paloma Cabanas Received Received
  211-P2 Growth hormone treatment for short stature associated with TRNT1 deficiency: a case series Yuezhen Lin Received Received
  212-P3 Height velocity and height gain in the first year of growth hormone (GH) treatment: predictive factors of good statural response in patients born small for gestational age Régis Coutant Received Received
  212-P1 Real-World Safety Data in a Cohort of Children with Noonan Syndrome Treated with Growth Hormone: Final Results from NordiNet International Outcome Study (IOS) and the ANSWER Program Pétur Benedikt Júlíusson Received Received
  212-P2 Novel case of short stature and co-occurrence of SHOX gene mutation and Fanconi Anemia Aristotle Panayiotopoulos Received Received
  213-P2 Different genetic causes of short stature in a family Alev Tulun Received Received
  213-P3 Role of Insulin like growth factors on the growth parameters in children with acquired hypothyroidism: An analysis. Ruchi Goel Received Received
  213-P1 Insights in promoter transactivation activity of CBX2. Dirk Hart Received Received
  214-P3 Two Siblings With Short Stature V. SRI NAGESH Received Received
  214-P1 In silico and in vitro studies of human SRD5A2 variants in search for activating variants explaining androgen excess reveal additional loss of function variants Efstathios Katharopoulos Received Received
  214-P2 Incidence of Cranial MRI abnormalities in Patients with Isolated Growth Hormone Deficiency: 20 Years of Results Nadia Amin Received Received
  215-P2 SYSTEMATIC PROSPECTIVE STUDY OF EYE FUNDUSCOPY BEFORE AND AFTER STARTING TREATMENT WITH GROWTH HORMONE IN 289 PATIENTS. Eduard Mogas Viñals Received Received
  215-P3 RHGH replacement therapy and side- effects: ? retrospective study of 10 years STAVROULA PARASTATIDOU Received Received
  215-P1 Mutations involving nuclear receptors and their cofactors as a major cause of 46,XX DSD Ken McElreavey Received Received
  216-P1 SDgeneMatch, a new tool to aid the identification of the genetic causes of DSD Ken McElreavey Received Received
  216-P2 Incidence and prevalence of growth hormone deficiency in the Russian Federation an analysis of two registries Maria Vorontsova Received Received
  217-P3 Comparison the Recombinant Human Growth Hormone(rhGH) Treatment in Children with Idiopathic Short Stature(ISS) and Growth Hormone Deficiency(GHD) YANQIN YING Received Received
  217-P2 The BSPED National Growth Hormone (GH) Audit: Trends in prescribing from 2013-2016 Leena Patel Received Received
  218-P3 Bone age maturation during the three years of growth hormone treatment in patients with idiopathic growth hormone deficiency and idiopathic short stature: Analysis of data from LG Growth Study Young Suk Shim Received Received
  218-P2 The Rationale and Design of TransCon GH Eva Mortensen Received Received
  218-P1 Primary gonadal dysgenesis in male 46,XY patients with NR5A1 variants predominantly affects Sertoli cell function Julia Hoppmann Received Received
  219-P1 Evaluation of Genetic Etiology in Patients with 46,XY Disorders of Sex Development:One Center Experience SUKRAN POYRAZOGLU Received Received
  219-P2 Baseline Demographics of the TransCon Growth Hormone Phase 3 heiGHt Trial Eva Mortensen Received Received
  219-P3 IS GROWTH HORMONE DEFICIENCY A CONTRIBUTOR TO SHORT STATURE IN CUTIS LAXA SYNDROME? Alice Albu Received Received
  220-P1 Pitfalls in the diagnosis of an infant with 46,XX DSD with Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency - the value of simultaneous genetic analysis to the diagnosis in DSD Jan Idkowiak Received Received
  220-P3 EFFECT OF SICKLE CELL DISEASE ON GROWTH AND PUBERTY Anjumanara Omar Received Received
  220-P2 The ZOMATRIP study: Four year combination therapy of GH and GnRHa in girls with a short predicted adult height during early puberty: adult height outcome. Raoul Rooman Received Received
  221-P1 High Mobility Group Box 1 (HMGB1) and Insulin-Like Growth Factor Binding Protein-2 (IGFBP-2) are increased, insulin decreased and IL-6 unchanged in Follicular Fluid (FF) from Polycystic Ovarian Syndrome (PCOS) MARIA E. STREET Received Received
  221-P3 Two Siblings with Alstrm Syndrome Ayse Nurcan Cebeci Received Received
  221-P2 GROWTH HORMONE TREATMENT IN CHILDREN BORN SMALL FOR GESTATIONAL AGE (SGA) Aleksandra Janchevska Received Received
  222-P2 Height perception of children with Growth Hormone Deficiency: influencing factors and links to psychosocial functioning Chrysoula Drosatou Received Received
  222-P1 A de novo missense mutation in the 4th zinc finger of the WT1 gene causes 46,XY and 46,XX DSD in two sibs Rita Agnes Bertalan MD PhD Received Received
  222-P3 Development of an Online Learn-pro Module to support Health Care Professionals knowledge about Growth and Puberty barbara Wardhaugh Received Received
  223-P2 Health lifestyle and obesity of adult patients with Congenital Isolated Growth Hormone Deficiency treated in childhood Zvi Laron Received Received
  223-P3 COELIAC DISEASE IN TURNER SYNDROME MORE FREQUENT THAN EXPECTED. BAZ OUIDAD Received Received
  223-P1 Sex-Differences in Reproductive Hormones during Mini-Puberty in Infants with Normal and Disordered Sex Development Marie Lindhardt Ljubucuc Received Received
  224-P2 Factors influencing Health Related Quality of Life in children/adolescents with Growth Hormone Deficiency Chrysoula Drosatou Received Received
  224-P3 A 14-year-old boy with Simpson- Golabi- Behmel syndrome- case report Beata Sawicka Received Received
  224-P1 TheExternalGenitaliaScoreto describe external genitalia in male and female infants. A Europeanmulticenter validation study Saskia van der Straaten Received Received
  225-P3 Central precocious puberty in a girl with Silver Russell syndrome Beata Wikiera Received Received
  225-P2 HEALTH-RELATED QUALITY OF LIFE AND PSYCHOSOCIAL FUNCTIONING IN YOUNG ADULTS BORN SGA AFTER GH/GNRHA TREATMENT Wesley Goedegebuure Received Received
  225-P1 Living with clitoromegaly:A qualitative interview study of parents responses to clitoromegaly in Congenital Adrenal Hyperplasia (CAH) with or without appearance altering surgery. Maia Thornton Received Received
  226-P1 You can put ideas into their heads: Parental concerns about childrens participation in DSD research. Maia Thornton Received Received
  226-P3 Etiologies of Short Stature in Pedaitric Endocrine Clinic in Northwest Region (Trakya) of Turkey Emine Dilek Received Received
  226-P2 Adherence to Treatment in Growth Hormone Deficient and Small for Gestational Age Patients Nave to EasypodTM in Mexico: Final Results of the EasypodTM Connect Observational Study (ECOS) Mel West Received Received
  227-P3 Auditing presentation, investigations and management of Turners syndrome Buddhi Gunasekara Received Received
  227-P2 GROWTH PATTERN AND FINAL HEIGHT OUTCOME IN CHILDREN WITH SEPTO-OPTIC DYSPLASIA AND ISOLATED HYPOPITUITARISM TREATED WITH rhGH IN A SINGLE CENTRE Manuela Cerbone Received Received
  227-P1 Testosterone levels in newborn boys and girls related to penile length, Anogenital distance (AGD) and External Genitalia Score (EGS) Jon Sigurdsson Received Received
  228-P2 Reliability of Clonidine Testing for the Diagnosis of Growth Hormone Deficiency in Children and Adolescents Anastasia Ibba Received Received
  228-P1 Clinical Factors That Determine Surgical Outcome Following Hypospadias Repair Fahad Aljuraibah Received Received
  228-P3 CHILDREN BORN SMALL FOR GESTATIONAL AGE: CATCH-UP GROWTH DURING THE FIRST FOUR YEARS OF LIFE concepcion martin Received Received
  229-P2 Area Under the Curve of Growth Hormone, an additional tool in assessing stimulation test results. Yonatan Yeshayahu Received Received
  229-P3 A Novel Heterozygous Pathogenic Variant in PORCN Gene Causing Focal Dermal Hypoplasia with Short Stature: Case Report and Literature Review DI WU Received Received
  229-P1 Prevalence of hypogonadism in prepubertal boys with cryptrochdism. Romina Grinspon Received Received
  230-P3 ENDOCRINOLOGICAL EVALUATION OF GIRLS WITH TURNER SYNDROME ATTENDING ALEXANDRIA UNIVERSITY CHILDRENS HOSPITAL Doaa Khater Received Received
  230-P1 Testicular ultrasound to stratify gonadal hormone references in a Norwegian study of male puberty Andre Madsen Received Received
  230-P2 Evaluation of Spontaneous Nocturnal GH Secretion: One versus two consecutive Nights Gunter Simic-Schleicher Received Received
  231-P3 A long follow-up in a young patient with Atypical Progeroid Syndrome scarano emanuela Received Received
  231-P1 Altered vascular function in boys with hypospadias- role of reactive oxygen species Angela Lucas-Herald Received Received
  231-P2 Relationship between growth velocity and change of serum insulin-like growth factor-1 (IGF-1), serum IGF binding protein-3 (IGFBP-3) concentrations, and IGFBP-3 promoter polymorphism during gonadotropin-releasing hormone agonist (GnRHa) treatment Seung Yang Received Received
  232-P1 Gonadectomy for Adults With DSD Conditions In The International Disorders of Sex Development Registry Angela Lucas-Herald Received Received
  232-P2 The predictive role of IGF-1 on irradiation-dependent growth hormone deficiency (GHD) in childhood cancer survivors (CCS) Alessandro Cattoni Received Received
  232-P3 GH treatment in Kabuki syndrome: a case report Elisa Guidoni Received Received
  233-P3 GH treatment in oto-spondylo-megaepiphyseal dysplasia: a case report Elisa Guidoni Received Received
  233-P1 Phenotypic And Genetic Assessment Of Boys With A Suspected XY Disorder Of Sex Development Malika Alimussina Received Received
  234-P1 Pediatricians Attitudes and Beliefs towards Transgender Persons Nitsan Landau Received Received
  234-P3 Hepatic glycogen synthasedeficiency associated with growth hormone deficiency: A case report Hakan Dneray Received Received
  234-P2 HIGH PROTEIN NUTRITIONAL SUPPLEMENTATION INCREASES SERUM IGF-I CONCENTRATIONS IN SHORT CHILDREN WITH LOW IGF-I Elin Mattsson Received Received
  235-P2 Hormonal predictors of growth hormone therapy effectiveness in children with short stature evidence from neural prediction model for final height Maciej Hilczer Received Received
  235-P3 Analysis of genetic mutations in a Chinese patient affected with Noonan Syndrome HUI HUANG Received Received
  235-P1 Diagnosis of adolescent Polycystic Ovary Syndrome (PCOS) according to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS Alexia Peña Received Received
  236-P2 Artificial neural networks for prediction final height in children with growth hormone deficiency. Anna Gavrilova Received Received
  236-P3 A novel homozygous mutation in ERCC8 cause Cockayne Syndrome a in a Chinese family HUI HUANG Received Received
  237-P3 Growth Hormon deficiency in identical twins with Gitelman Syndrome due to compound heterozygous mutation (p.R80fs35/p.K957X ) of the SLC12A3 gene and the evaluation of the response to growth hormone replacement therapy Huseyin Demirbilek Received Received
  237-P2 Predictors of poor response to growth hormone therapy in children with short stature evidence from neural prediction model for final height Joanna Smyczynska Received Received
  238-P2 TITLE-Growth Hormone therapy and its challenges in GH Deficient cases in a multinational population-a sneak-peek DEEPTI CHATURVEDI Received Received
  238-P3 Title: Hypothyroidism and Growth Hormone (GH) Deficiency, A Spotlight on De Novo Chromosomal 20p11.2 Deletion Idris Mohammed Received Received
  238-P1 Effect of intrauterine growth restriction on ovarian follicle pool in rats Valentina Pampanini Received Received
  239-P2 HEART AND AORTA ANOMALIES IN TURNER SYNDROME AND RELATION WITH KARYOTYPE Asl&305; Derya Kardelen Received Received
  239-P1 Sustainability of estradiol drug concentrations in cut matrix patches; a study of different brands with potential use for pubertal induction Carina Ankarberg-Lindgren Received Received
  239-P3 PHARMACOECONOMIC AND ADHERENCE ANALYSIS in GROWTH HORMONE ACCORDING TO GALENIC PRESENTATION In vivo study vs in vitro Ignacio Diez Received Received
  240-P3 The expression of cytokines in SGA children throughout lactation allows to characterize early the type of cath-up Ignacio Diez Received Received
  240-P2 The validation of an automated bone age assessment in girls with Turner syndrome a pilot study Ondrej Soucek Received Received
  240-P1 Anti-Mullerian Hormone (AMH) concentrations and reduced Appendix Testis Estrogen Receptor expression in Cryptorchidism Eirini Kostopoulou Received Received
  241-P1 The comparisons of the adult height gain and the menarchal age of the girls with Central Precocious Puberty after Gonadotropin Releasing Hormone agonist alone and those treated with combined Growth Hormone therapy SE YOUNG KIM Received Received
  241-P3 SMALL STATURE: A singular difference for accessing to job Ignacio Diez Received Received
  241-P2 Turner Syndrome and Autoimmune Thyroid Disease: pecularities of evolution in 93 Turner Syndrome patients. CRISTINA DUMITRESCU Received Received
  242-P3 A case of Hutchinson-Gilford Progeria Syndrome (HGPS) due to a pathogenic LMNA variant c.433GA (p.Glu145Lys): Growth hormone administration failed to improve growth and long-term outcome Ledjona Toni Received Received
  242-P2 Unusual clinical manifestations in Turner syndrome Natallia Akulevich Received Received
  242-P1 AMH LEVEL OF INFANTS WITH PREMATURE THELARCHE AND POSSIBLE RELATIONSHIP BETWEEN AMH AND MINI-PUBERTY nursel muratoglu sahin Received Received
  243-P2 Effect of combined growth hormone and estrogen treatment on the lipid profile and systolic function of the left ventricle in girls with Turner syndrome (TS) Tatiana Shiryaeva Received Received
  243-P3 Increased serum activity of liver aminotransferases in young patients with Turner Syndrome Ma&322;gorzata Wójcik Received Received
  243-P1 Circulating makorin ring finger protein 3 levels predict central precocious puberty in girls Hwal Rim Jeong Received Received
  244-P2 Familial Turner Syndrome: Case Report Jimena Lopez Dacal Received Received
  244-P1 Polycystic Ovarian Syndrome in Adolescents: Characterising the Clinical Phenotype and the Role of Precision Medicine Harriet Gunn Received Received
  245-P2 Clinical review of 7 patients affected with 49,XXXXY syndrome Jacobo Pérez Sánchez Received Received
  245-P1 Thyroid function in central precocious puberty girls Hyo-Kyoung Nam Received Received
  246-P2 Poor weight gain in Prader-Willi Syndrome not always over-restriction consider Coeliac Disease Mina Lateva Received Received
  246-P1 Clinical phenotypes and mutation spectrum of patients with isolated gonadotropin-releasing hormone deficiency in a single academic center Han-Wook Yoo Received Received
  246-P3 Microduplication of 3p25.3 and 4p23 regions in a patient with multiple congenital anomalies, congenital hypothyroidism and adrenogenital syndrome. massimo barreca Received Received
  247-P3 A Rare Chromosomal Disorder, Trisomy 4p MERVE NUR HEPOKUR Received Received
  247-P2 Growth Hormone Unmasked Laryngomalacia and Worsened Obstructive Sleep Apnea in Infants with Prader-Willi Syndrome Parisa Salehi Received Received
  248-P2 How frequent are growth charts used in paediatric clinics? An audit of growth chart use in a Scottish district general hospital John Schulga Received Received
  248-P1 Early determinants of thyroid function outcome in children with congenital hypothyroidism and a normally located thyroid gland: a regional cohort studyCarole Saba Carole Received Received
  248-P3 Prediction of response to growth hormone treatment in Korean girls with Turner syndrome Mo Kyung Jung Received Received
  249-P2 GrowInform a campaign for early diagnosis and treatment of growth disorders Rosica Stoycheva Received Received
  250-P2 Growth and body composition of term healthy Indian infants from birth to 2 years of age Vandana Jain Received Received
  250-P3 Prader-Willi Patient with Rectal Bleeding Experience in Center for Rare Endocrine Disordesrs in Varna, Bulagria. Nikolinka Yordanova Received Received
  250-P1 Thyroid scintigraphy in the diagnosis of Congenital Hypothyroidism Chris Worth Received Received
  251-P3 MOSAICISM 47XXX/45X0, A CASE REPORT Renata Pinto Received Received
  251-P1 Congenital hypothyroidism (CH) with delayed TSH elevation: the importance of the second-screening strategy and the evolution of CH in preterm infants Silvana Caiulo Received Received
  251-P2 Growth, body composition and metabolic parameters during childhood in a cohort of children born with a small for gestational age M. Loredana Marcovecchio Received Received
  252-P3 Factors Affecting the Selection of Injection Location during Self-Therapy for Growth Hormone Therapy among Patients 10-15 Years old Rotem Diamant Received Received
  252-P2 Final Results of NordiNet International Outcome Study: Key Outcomes in Paediatric Patients Michel Polak Received Received
  252-P1 Morning versus Bedtime Levothyroxine Administration: What is the Choice of Children? ONUR AKIN Received Received
  253-P2 INFLUENCE OF PUBERTY ON ADULT HEIGHT OF SGA CHILDREN TREATED WITH GH Juan Pedro Lopez Siguero Received Received
  253-P3 Tall Stature: A Diagnosis Is Somtimes Difficult kherra sakina Received Received
  253-P1 LONG TERM COMPARISON BETWEEN LIQUID AND TABLET FORMULATIONS OF L-THYROXINE (L-T4) IN THE TREATMENT OF CONGENITAL HYPOTHYROIDISM (CH) Maria Cristina Vigone Received Received
  254-P3 Title: Woodhouse-Sakati Syndrome: Clinical and Molecular Study on a Qatari Family with C2orf37Gene MutationMCEPASTEBIN Katarina Gluic Received Received
  254-P2 BURDEN AND IMPACTS OF DAILY RECOMBINANT HUMAN GROWTH HORMONE (r-hGH) INJECTIONS IN GROWTH HORMONE DEFICIENT (GHD) PAEDIATRIC PATIENTS Roger Lamoureux Received Received
  254-P1 Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH beta subunit Gene TARIK KIRKGOZ Received Received
  255-P1 Patterns of thyroglobulin levels in infants referred with high TSH on newborn screening, compared with iodine-sufficient healthy controls wafa kallali Received Received
  255-P3 Factors affecting height velocity in normal prepubertal children Seul Ki Kim Received Received
  255-P2 Clinical and cost-effectiveness of GH treatment for children in Wales Raluca-Monica Pop Received Received
  256-P3 Low dose Growth Hormone using IGF1 dose titration is associated with sustained optimal growth in a child with both Turner and Down syndrome. Sharon Lim Received Received
  256-P2 Bone mineral density and body composition of young adults who were born small for gestational age and treated with growth hormone, after treatment completion.AN ANGELA ASCASO MATAMALA Received Received
  257-P1 Results of the hTPO mutational screening in Bulgarian patients with congenital hypothyroidism (CH) Iva Stoeva Received Received
  258-P3 LATE REFERRAL OF SIBILINGS WITH COMBINED PITUITARY HORMONE DEFICIENCY (PROP1) Snijezana Hasanbegovic Received Received
  258-P2 Clinical and Molecular Analyses of 24 Patients with Beckwith-Wiedemann Syndrome WEI LU Received Received
  259-P3 17p13.1 Microduplication Syndrome in a child with familial short stature and growth hormone deficiency: A short case report SOFIA LEKA Received Received
  259-P2 Unusual case of combination of Beckwith-Wiedemann Syndrome and SHOX gene deficiency Marco Pitea Received Received
  259-P1 A novel mutation of IGSF1 gene ELLADA SOTIRIDOU Received Received
  260-P3 PRADER WILLI SYNDROME: CLINICAL PROFILE Vasundhara Chugh Received Received
  260-P2 An Irish regional study of Paediatric Growth Hormone Deficiency (CO-GHD): Classification of causes and factors associated with persistent GHD at transition mariana Grace Received Received
  260-P1 Multinodular goiter in childhood: a diagnostic gateway for screening DICER1 syndrome isabelle OLIVER PETIT Received Received
  261-P1 A novel DICER1 mutation identified in a family with the multinodular goiter of children Keisuke Nagasaki Received Received
  261-P2 Two different variants of short stature homeobox-containing gene (SHOX) mutation in the same family Stefanie Graf Received Received
  261-P3 Leri-Weill Syndrome phenotype with atypical cytogenetic finding Vilhelm Mladenov Received Received
  262-P2 Identification of a novel heterozygous ACAN mutation in a patient with non-syndromic short stature Partenop Cristina Received Received
  262-P3 Deletion of 12q12 increases the risk of growth retardation and intellectual disability Ying Weng Received Received
  263-P1 Expression of ZnT8 transporter in thyroid tissues from patients with immune and non-immune thyroid diseases Artur Bossowski Received Received
  263-P2 Genetic investigation of Short Stature: a case report of Complex Constitutive rearrangement involving chromosome 15 Renata Pinto Received Received
  264-P2 Targeted/exome sequencing identified mutations in 55 Chinese children diagnosed with Noonan syndrome and a autosomal recessive form associated with LZTR1 variants Xin Li Received Received
  265-P3 Insulinoma as initial presentation of Multiple Endocrine Neoplasia type 1 Ada Borowiec Received Received
  265-P2 A Novel Heterozygous Missense Variant in the LZTR1 Gene as a Cause of Noonan SyndromeA Novel Heterozygous Missense Variant in the LZTR1 Gene as a Cause of Noonan Syndrome Sumito Dateki Received Received
  265-P1 HLA alleles and amino acid variants of HLA-A, -B, -C, -DRB1, -DQB1, -DPB1 molecules in early-onset autoimmune thyroid disease. Won Kyoung Cho Received Received
  266-P1 Childhood thyroid autoimmunity and relation to islet autoantibodies in children at risk for type 1 diabetes Berglind Jonsdottir Received Received
  266-P2 A novel FGFR1 mutation in Kallmann syndrome with growth hormone deficiency Maria Chiara Pellegrin Received Received
  266-P3 Assessment of ovarian reserve in young women with Hashimoto thyroiditis - a pilot study Anna Wedrychowicz Received Received
  267-P3 Unusual clinical presentation of autoimmune polyendocrinopathy type 1. Federico Baronio Received Received
  267-P1 Evaluation of serum concentrations of ed cytokines OPG and sRANKL in the diagnosis of autoimmune thyroid disease in children Marek Niedziela Received Received
  268-P2 A new mutation in IHH gene causing severe short stature. adalgisa festa Received Received
  268-P1 Analysis of zinc- transporter ZnT8 autoantibodies in children and adolescents with autoimmune thyroid diseases Justyna Michalak Received Received
  268-P3 Glycemic abnormalities and Normal Thyroid Function in Adolescent Survivors of Childhood Acute Lymphocytic Leukemia Who Required Repeated Packed Red Cell Transfusion during treatment Ashraf Soliman Received Received
  269-P1 The association between TSHR, IFIH1 and ETV5 polymorphisms with Graves disease and diabetes mellitus type 1 in children Karolina Stozek Received Received
  269-P2 CASE REPORT: ELLIS VAN CREVELD SYNDROME WITH A NOVEL MUTATION elif sb Received Received
  269-P3 GRAVES DISEASE IN CHILDREN WITH T1DM: A REPORT OF THREE CASES Ngoc Can Thi Bich Received Received
  270-P3 Case report: Neonatal McCune-Albright syndrome with juvenile ovarian granulosa cell tumor in a 4 months old girl Esther Schulz Received Received
  270-P2 A homozygous pathogenic variant in the TRHR gene in a boy who presented with severe familial short stature and central hypothyroidism Luká Plach Received Received
  271-P3 Polyostotic Fibrous Dysplasia of McCune Albright Syndrome responding to intravenous Zoledronate therapy Ganesh HK Received Received
  271-P2 Unexpected growth patterns in Branchio-Oto-Renal syndrome. Emma Clarke Received Received
  272-P3 Two Cases of Costello Syndromeand Literatures Review Zhuan-nan Jiang Received Received
  272-P2 Mild autistic spectrum disorder in a 33 year-old male Japanese patient with Temple syndrome Shuichi Yatsuga Received Received
  273-P3 ENDOCRINE COMPLICATIONS IN BETA-THALASSAEMIA MAJOR CHILDREN Mirela Iancu Received Received
  273-P2 Seventeen-year observation in a Japanese female case of Tatton-Brown-Rahman syndrome: an overgrowth syndrome with intellectual disability Yoko Miyoshi Received Received
  274-P2 KBG syndrome: our experience and unreported clinical features. emanuela scarano Received Received
  274-P3 The case of combination of multinodular goiter and Sertoli-Leydig cell ovarian tumor due to mutation in DICER1 gene Nina Makretskaya Received Received
  275-P3 Unusual case of Autoimmune Polyglandular Syndrome. Nino Abdushelishvili Received Received
  275-P2 Growth of Infants Born by Intracytoplasmic sperm injection (ICSI) Technique Ashraf Soliman Received Received
  276-P3 AUTOIMMUNEPOLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY: A CASE REPORT Ozlem Nalbantoglu Received Received
  276-P2 Earlier mothers age at menarche is a risk factor of daughters early menarche and short stature in young Korean female: Epidemiologic study JUNG SUB LIM Received Received
  277-P2 Pulling the brakes Catch down growth: a phenomenon for achieving mid-parental height centile after acquired, all-cause, brain injury Fabian Bernhard Thaddus Kraus Received Received
  277-P3 WOLMAN DISEASE: LONG-TERM ENDOCRINE AND METABOLIC COMORBIDITIES Rachel Bello Received Received
  278-P2 Effects of inhaled corticosteroids and montelukast on growth and body mass index in children with asthma onur AKIN Received Received
  279-P3 NEAR ELECTROMAGNETIC FIELDS - INDUCED SYNDROME: UNSUSPECTED AND NEWLY RECOGNISED STYLIANI GERONIKOLOU Received Received
  280-P3 POLYCYSTIC OVARY SYNDROME GENE/GENE PRODUCTS INTERACTION NETWORK STYLIANI GERONIKOLOU Received Received
  280-P2 Skeletal Disproportion And Growth Impairment In Glucocorticoid Treated Boys With Duchenne Muscular Dystrophy Kao Kung-Ting Received Received
  281-P3 BASAL METABOLIC RATE AS MODERATOR OF INFLAMMATION IN PCOS STYLIANI GERONIKOLOU Received Received
  281-P2 A Novel Mutation in the SLC2A2 gene in a 19-year-old Female with Diabetes Mellitus and Renal Tubular Acidosis: A Therapeutic Conundrum Sanaa Sharari Received Received
  282-P3 Insight of differential diagnosis of DAX-1 from two patients with elevated testosterone in early infancy Tang Li Received Received
  282-P2 VESICO-URETERAL REFLUX AND EFFECT ON GROWTH INDICES. Georges Nicolas Received Received
  283-P3 Rapid onset and progression of chronic kidney disease in a child with Autoimmune Polyglandular Syndrome Type 1. Vasiliki Rengina Tsinopoulou Received Received
  284-P3 Infant with osteogenesis imperfecta and panhypopituitarism: a case report Noor Arliena Mat Amin Received Received
  284-P2 ENDOCRINE AND METABOLIC COMPLICATIONS IN CHILDREN AND ADOLESCENTS WITH SICKLE CELL DISEASE: AN ITALIAN COHORT STUDY Lorenzo Iughetti Received Received
  285-P2 Bone marrow failure in Mc Cune Albright Syndrome Katja Wechsung Received Received
  285-P3 PANHYPOPITUITARISM WITH TALL STATURE DIAGNOSED IN A 20 YEARS OLD BOY Andrea Forrester Received Received
  286-P3 Post-traumatic hypopituitarism caused by pituitary stalk transection Anna Ruszala Received Received
  286-P2 Final adult height, Insulin-like Growth Factor 1 (IGF-I) concentration and endocrine complications in adolescents and young adults with -thalassemia major (BTM) who received oral iron chelation (OIC) in comparison with those who did not use OIC ashraf soliman Received Received
  287-P3 Invasive macroprolactinoma with cabergoline induced cerebrospinal fluid rhinorrhoea in childhood Antonia Dastamani Received Received
  287-P2 Endocrine challenges in patients with thalassemia Tanja Christa Haamberg Received Received
  288-P3 Bilateral optic nerve hypoplasia revealing septo optic dysplasia or De Morsier syndrome: A case report. ARIBI YAMINA Received Received
  288-P2 Can oral iron chelation therapies reduce endocrine complications in -thalassemia major patients? PARASTOO ROSTAMI Received Received
  289-P2 Statural Growth and Endocrinopathies in Relation to Liver Iron Content (LIC) and Insulin-Like Growth Factor 1 (IGF-I) Concentration in Adolescents with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD) ASHRAF Soliman Received Received
  290-P3 An Interesting Etiology in Childhood Central Diabetes Insipidus HIBERNOMA Aya Trel Ergr Received Received
  290-P2 Successful treatment of severe atopic dermatitis with calcitriol and paricalcitol in an 8-year old girl. Christina Bothou Received Received
  291-P3 Neonatal panhypopituitarism with hypoglycemia, edema, inspiratory stridor and cholestasis Benita Momm Received Received
  291-P2 Hypoglycemia in adolescence as the presenting sign of familial MEN1 Justine BAILLEUL Received Received
  292-P3 MRI changes in time after cranial irradiation, and their relation with pituitary function in survivors of childhood medulloblastoma Christi van Ommen Received Received
  292-P2 ALDOSTERONE, RENIN, SODIUM AND POTASSIUM EXCRETION IN NORMOTENSIVE PREPUBERTAL CHILDREN Alejandro Martinez-Aguayo Received Received
  294-P2 BRITISH SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY AND DIABETES PEER REVIEW OF SPECIALISED PAEDIATRIC ENDOCRINOLOGY SERVICES IN THE UK - EVALUATION OF THE PROCESS John Schulga Received Received
  294-P3 Growth hormone deficit associated to complex arteriovenous malformation case report Mirela Mogoi Received Received
  296-P3 Analysis of Influencing Factors on Bone Maturation in Girls with Central Precocious Puberty(CPP) Gi-min Lee Received Received
  296-P2 Military conflict at the east of ukraine and physical development of children and adolescents Svetlana Turchina Received Received
  297-P3 Is Prematre Adrenarch Associated With Precocious Puberty Via Kisspeptin? GUL D&304;REK Received Received
  297-P2 POLYCYSTIC OVARY SYNDROME METABOLIC SYNDROME PREDISPOSITION IN PUBERTY STYLIANI GERONIKOLOU Received Received
  298-P2 Fanconi-Bickel Syndrome in Sudanese children, Case series Salwa Elhassan Received Received
  299-P2 The N309K Pro-Protein Convertase Type 1 (PCSK1) Gene Mutation Causes Lack of Spontaneous Puberty and Primary Amenorrhea Ulla Najwa Abdulhag Received Received
  299-P3 A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding Harjoedi Harjoedi Received Received
  300-P3 Evaluation of Cases with Pubertal Gynecomastia Havva Nur Kendirci Received Received
  300-P2 Somatostatin Experiment in Prohormone Convertase Deficiency emine demet akba&351; Received Received
  301-P3 A case of central diabetes insipidus developed 4 years after the non-CNS-risk unifocal bone lesion of Langerhans cell histiocytosis Hisae Nakatani Received Received
  301-P2 Efficacy and safety of triptorelin 3-monthformulationin patients with centralprecocious puberty and BMI evaluation. Rossella Gaudino Received Received
  302-P3 EFFECT OF TRIPTORELINE IN PATIENTS WITH CENTRAL PRECOCIOUS PUBERTY AT CHILDRENS HOSPITAL 1.HCMC.VIET NAM Huyen Tran Received Received
  302-P2 Triptorelin Test in Diagnosing Central Precocious Puberty Rade Vukovic Received Received
  303-P3 Morning unstimulated hormone, a good screening tool for diagnosing central precocious puberty. Dong Min Lee Received Received
  303-P2 Foot length growth is a novel marker of early puberty Ben Balzer Received Received
  304-P2 Ultrasound-based measurements of testicular volumeObserver agreement and comparison with Prader orchidometry Ninnie Oehme Received Received
  307-P3 Premature adrenarche and pseudohypoparathyroidism mechanistically linked or coincidence? Jessica Odone Received Received
  307-P2 The effect of GnRH-analogue therapy on the quality of life of patients with Central precocious puberty and their families Laura Lucaccioni Received Received
  308-P2 A NOVEL INACTIVATING COMPOUND HETEROZYGOUS MUTATION IN KISS1R/GPR54: CASES OF THREE SIBLINGS Ozlem Nalbantoglu Received Received
  309-P3 GLP-1 receptor agonist in a patient with craniopharyngioma-related obesity. Maria-Christina Antoniou Received Received
  309-P2 MKRN3 gene mutations in a cohort of patients with central precocious puberty Magdalena Avbelj Stefanija Received Received
  310-P2 Can basal levels of luteinizing hormone (LH) replace the GnRH test in the diagnosis of precocious puberty in girls? Juan Llano Received Received
  311-P2 Incidence of delayed puberty. A population-based study in a county in central Sweden. Maria Rodanaki Received Received
  311-P3 Congenital hypopituitarism associated with complex cranio-vertebral junction anomalies Mariella Valenzise Received Received
  312-P2 Observer agreement in ultrasound assessment of pubertal breast development Ingvild Srvold Bruserud Received Received
  312-P3 Premature thelarche followed by acute lymphoblastic leukemia in a 1,5 year old girl Ana Stamatova Received Received
  313-P3 Two cases of non-syndromic congenital unilateral hypoplasia in one family Ana Stamatova Received Received
  313-P2 Neuroendocrine consequences of Hypothalamic Hamartoma and their Imaging (MRI) and Surgery Correlates. Beatriz Corredor Andrés Received Received
  314-P3 Klinefelter Syndrome with Ambiguous Genitalia in a Child nur rochmah Received Received
  314-P2 THE START PREDICTORS OF PUBERTY IN BOYS WITH CONSTITUTIONAL DELAY OF PUBERTY Oleg Latyshev Received Received
  315-P3 The change in growths velocity in patients with premature puberty receiving treatment with analogues of lyuliberin Olga Berseneva Received Received
  316-P2 Gonadotropin Levels And Frequency Of Testosterone Supplementation In Adolescents With Klinefelter Syndrome XANTHIPPI TSERETOPOULOU Received Received
  316-P3 THE EFFICACY OF TREATMENT IN VIETNAMESE CHILDREN WITH CENTRAL PRECOCIOUS PUBERTY Quynh Huynh Thi Vu Received Received
  317-P3 THE CHARACTERISTICS OF CENTRAL PRECOCIOUS PUBERTY AT CHILDRENS HOSPITAL 2 IN VIETNAM Quynh Huynh Thi Vu Received Received
  318-P2 SOX3 gene duplication associated with midline CNS malformations, hypopituitarism and neurodevelopmental abnormalities: 5 unrelated cases Garima Chawla Received Received
  318-P3 SIG (Special Interest Group)-ENDOPED/RUTE (Brazil): Seven years integrating pediatric endocrinology centers throughout the country Ricardo Arrais Received Received
  319-P2 AN 18 MONTH OLD BOY WITH HYPOGLYCEMIC CONVULSION AND OBESITY DUE TO POMC DEFICIENCY Sare Betul Kaygusuz Received Received
  319-P3 The relationship between prolactin and development of puberty in girls with early breast development Seong Yong Lee Received Received
  320-P3 Central Precocious Puberty appeared in infancy period in a patient of Sotos Syndrome tu&287;ba etin Received Received
  320-P2 Pituitary stalk interruption syndrome (PSIS) is not a rare cause of the congenital hypopituitarism Erdal Eren Received Received
  321-P2 Pallister Hall syndrome: an unusual case of central precocious puberty, prolonged vaginal bleeding, gelastic seizures and polysyndactyly in a 7 month old infant. María Clemente Received Received
  321-P3 Gonadal tumor incidence in patients with disorders od sex development containing Y chromosome or Y-derived sequences - experience from one clinical center Aleksandra Antosz Received Received
  322-P3 New method of surgical correction of female hypospadias in girls with disorders of sex development and stenosis of artificial introitus Alexander Anikief Received Received
  322-P2 PRIMARY EMPTY SELLA SYNDROME AND CLNICAL ENDOCRINE POLYMORPHISMS IN CHILDREN. A REPORT OF 15 CASES. SIMON KAYEMBA-KAYS Received Received
  323-P2 Growth hormone deficiency (GHD) in a patient with persistence of the craniopharyngeal canal with cephalocele Silvana Caiulo Received Received
  324-P2 Endocrine-metabolic characterization of pediatric patients with craniopharyngioma. A single-centre cohort study. Stefania Pedicelli Received Received
  324-P3 Challenges in managing 46, XY Partial gonadal dysgenesis in Saudi Arabia AMIR BABIKER Received Received
  325-P2 Growth Hormone (GH) secreting pituitary adenomas in Paediatric Practice: 5 cases over 20 years in a single tertiary NeuroEndocrine Centre. Elspeth Brooker Received Received
  325-P3 A paternally inherited NR5A1 mutation in a case of 46,XY partial gonadal dysgenesis Andréa Maciel-Guerra Received Received
  326-P3 CLINICAL PRESENTATION AND CHARACTERISTICS OF DSD IN KENYAN CHILDREN AND ADOLESCENTS Anjumanara Omar Received Received
  326-P2 Pituitary adenomas in children and adolescents: a retrospective single-centre analysis Thomas Breil Received Received
  327-P2 Changes in body composition in male adolescents with GH deficiency are diagnostic during transition Gerhard Binder Received Received
  327-P3 Evolutive profile of pauci-symptomatic forms of Mc Cune Albright syndrome audrey cartault Received Received
  328-P3 A 45X0/46XY Girl Diagnosed with Prepubertal FSH Elevation Belma Haliloglu Received Received
  328-P2 Serum levels of antimllerian hormone and inhibin B in central precocious puberty before and during treatment with GnRH agonist. Hwal Rim Jeong Received Received
  329-P2 Gender-related differences in etiological distribution of organic causes of central precocious puberty Dogus Vuralli Received Received
  329-P3 About a case of Leydig cell tumor associated with central precocious puberty bensalah Meryem Received Received
  330-P2 Final adult height in girls with idiopathic central precocious puberty treated with monthly leuprorelin acetate VS triptorelin acetate Voraluck Phatarakijnirund Received Received
  330-P3 Gender dysphoria Birgit Lidwall Received Received
  331-P2 The impact of Central Precious Puberty on health-relatedqualityoflifeand social, emotive and behavioral competences among children treated with GnRHa. Rossella Gaudino Received Received
  331-P3 GnRH Analogues and Cross-Sex Hormonal therapy: side effects in Transgender Youth Cristina Mora Palma Received Received
  332-P3 Klinefelter syndrome with low gonadotropin levels Daria Berdyugina Received Received
  332-P2 Basal Serum LH Level as a Diagnostic Test for Girls with Early Phase of Central Precocious Puberty Somboon Wankanit Received Received
  333-P2 Determination of urinary metabolic profiles of children with central and peripheral precocious puberty derya bulu&351; Received Received
  333-P3 YOUNG MALE ADOLESCENT WITH GENDER DYSPHORIA (GD)/GENDER INCONGRUENCE- A CASE PRESENTATION Eirini Dikaiakou Received Received
  334-P3 Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty and early puberty Eun Young Kim Received Received
  334-P2 Hypertension during GNRH analogues therapy in a 10-year-old girl massimo barreca Received Received
  335-P2 The Effect Of Polychlorinobiphenyls On Premature Puberty In Girls Samim zen Received Received
  335-P3 DSD in Ukraine: our experience Evgenia Globa Received Received
  336-P2 A novel mutation in 5 untranslation region of Makorin ring finger 3 gene associated with the familial precocious puberty wenli Lu Received Received
  336-P3 A Turkish family with 46,XY disorder of sex development due to 17b-hydroxysteroid dehydrogenase type 3 deficiency fatih grbz Received Received
  337-P2 A case of testotoxicosis due to a constitutive mutation of the LH receptor initially presented as a central precocious puberty at 3 years old. Valérie Porquet-Bordes Received Received
  337-P3 Normal External Genitalia in a Female with Classic, Salt-Wasting 21-hydroxylase deficiency Hadeel Alsarraj Received Received
  338-P2 Physical assessment in Chinese children with 5a-reductase type 2 de?ciency Xiu Zhao Received Received
  338-P3 OVARIAN LEYDIG CELL TUMOR IN AN 8 YEARS OLD GIRL MISDIAGNOSED AS CONGENITAL ADRENAL HYPERPLASIA DUE TO ELEVATED 17-HYDROXI-PROGESTERONE Hernan Garcia Received Received
  339-P3 Analysis of genetic mutations in a Chinese pedigree affected with idiopathic hypogonadotropic hypogonadism Syndrome HUI HUANG Received Received
  339-P2 Results of exome sequencing in disorders of sex development Marlies Kempers Received Received
  340-P2 Awareness is the key: Heavy delay in diagnosis of 17--Hydroxysteroid-Dehydrogenase III deficiency (17bHSD3D) and other insights and conclusions from a cohort of ten 17bHSD3D patients in Germany. Jakob Meinel Received Received
  341-P3 Cytogenetic spectrum of Ovotesticular Disorder of Sex Development in Egyptian DSD patients inas mazen Received Received
  341-P2 Evaluation of Three Patients with 46,XY Gonadal Dysgenesis Due to Desert Hedgehog Gene Mutations SUKRAN POYRAZOGLU Received Received
  342-P2 In-silico gene-protein analysis and clinical phenotype characterisation of three novel NR5A1/SF1 gene mutations presenting with 46,XY DSD Rieko Tadokoro Cuccaro Received Received
  343-P2 Clinical, biochemical, structural and functional characterization of a novel P450 oxidoreductase mutation causing virilization in a 46,XX patient Núria Camats Received Received
  343-P3 Genital abnormalities and management outcomes as seen in the University of Port Harcourt Teaching Hospital Iroro Yarhere Received Received
  344-P3 A case report: A girl with 46,XY karyotype and disorder of androgen synthesis Jasna uput Omladi&269; Received Received
  344-P2 Copy-Number Variations of the Human Olfactory Receptor Gene Family in Patients with Macromastia and Prepubertal Gynecomastia Asl&305; Derya Kardelen Received Received
  345-P3 THE POSITIVE EFFECT OF THE LOW-DOSE CONTRACEPTIVE ON THE COURSE OF CYSTIC FIBROSIS IN THE ADOLESCENT FEMALE Juliana Ferenczova Received Received
  345-P2 Histopathologic characterization of patients with 46,XX testicular and ovotesticular disorders of sex development. Esperanza Berensztein Received Received
  346-P2 Current medical care of children and adolescents with disorders/differences of sex development in Switzerland Grit Sommer Received Received
  346-P3 Ovotesticular Disorder of Sexual Development: 31 cases followed-up in a single-center in Brazil Leandra Steinmetz Received Received
  347-P2 Clinical, Laboratory and Molecular Genetic Findings of Patients with 17-Hydroxysteroid Dehydrogenase3 Deficiency SUKRAN POYRAZOGLU Received Received
  347-P3 Genital swelling and ovarian stimulation syndrome in an extremely preterm infant Maria Cristina Azcona Received Received
  348-P3 Significant penile growth with local DHT-gel in an infant with 17beta-HSD-deficiency Maria Halldin Stenlid Received Received
  348-P2 Revisiting The Diagnosis: Next Generation Sequencing (NGS) Identifies Concurrence Of PAIS In A Previously Reported Case Of Klinefelter Syndrome (47,XXY) With Hypospadias. Zainaba Mohamed Received Received
  349-P2 A 46,XX female with WT1 mutation, congenital nephrotic syndrome and a complex disorder of sex development Sara Ciccone Received Received
  349-P3 Mother and baby diagnosed Noonan syndrome with dysmorphic findings Mehmet Keskin Received Received
  350-P2 Psychological gender features and social abilities and in adolescent girls influence of obesity and hyperandrogenism Agnieszka Zachurzok Received Received
  351-P3 A Case Report of Spironolactone Treatment for Beckers Nevus Associated Ipsilateral Breast Hypoplasia Abhilasha Banerjee Received Received
  351-P2 Two unrelated cases of severe insulin resistance due to insulin receptor mutation discovered during adolescence azgal maryam Received Received
  352-P2 A Systematic Review Of Reported Outcomes For Hypospadias Tina Lund Leunbach Received Received
  352-P3 NEW MUTATIO IN 5 ALFA REDOCTASE: A five-month-old infant with a karyotype of 46 xy setila dalili Received Received
  353-P3 A NOVEL COMPOUND HETEROZYGOUS MUTATION IN CYP19A1 RESULTING IN AROMATASE DEFICIENCY WITH NORMAL GONADOTROPIN LEVELS AND OVARIAN TISSUE Sezer Acar Received Received
  353-P2 Young transgender peoples attitudes to fertility preservation and practice elena Monti Received Received
  354-P2 ETIOLOGY OF DISORDERS OF SEX DEVELOPMENT IN KENYAN CHILDREN AND ADOLESCENTS Anjumanara Omar Received Received
  354-P3 Emblematic case CAH Silvia Chahin Received Received
  355-P3 The Republic of Colombia has a constitutional jurisprudential precedent identified as T622 of 2014, this sentence reaffirms the importance of the accurate diagnosis of INTERSEXUAL patients and updates how the state looks at them. Silvia Chahin Received Received
  355-P2 Adiponectin as a marker of peripheral insulin resistance in adolescents with polycystic ovarian syndrome (PCOS) and as a tool to suspect insulin receptor defects Analía Freire Received Received
  356-P3 Paediatric doctors experience and knowledge of the initial management of neonatal ambiguous genitalia Sinead McGlacken-Byrne Received Received
  356-P2 Diagnostic experiences and concerns in adolescents with polycystic ovary syndrome Alexia Pena Received Received
  357-P3 A case of Transverse Testicular Ectopia with Persistant Mllerian Duct Syndrome: A novel AMH gene mutation Suna KILIN Received Received
  357-P2 Impact of hydrocortisone treatment on clitoral size during first year of life in girls with Congenital adrenal hyperplasia (CAH) Johan Svensson Received Received
  358-P3 Argentinean first experience with transgender children and youths Veronica Figueroa Received Received
  358-P2 Persistent Mullerian duct syndrome: Rare but important aetiology of an inguinal hernia and cryptorchidism in boys Abdullah Bereket Received Received
  359-P3 Long-term follow-up in a Chinese child with lipoid congenital adrenal hyperplasiadue to STARmutation Xiu Zhao Received Received
  359-P2 CLINICAL, HORMONAL AND METABOLIC PROFILE IN ADOLESCENT GIRLS TREATED WITH GONADOTROPIN RELEASING HORMONE AGONIST FOR IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY Madalina Vintila Received Received
  360-P2 SPONTANEOUS PREGNANCIES IN FEMALE SURVIVORS OF CHILDHOOD HEMATOLOGICAL MALIGNANCIES POST ALLOGENEIC HAEMOPOIETIC STEM CELL TRANSPLANTATION Samantha Lai Ka Lee Received Received
  361-P2 Towards an integrated approach to diagnosis of 46,XY disorder of sex development. Zofia Kolesinska Received Received
  362-P3 Graves Disease in a Pediatric Population: results from the last 17 years at a Pediatric Endocrinology Unit Ana Antunes Received Received
  363-P3 Acquired severe hypothyroidism in children forgotten or unbelievable diagnosis in a time of large and easy availability of thyroid tests? Anna Kucharska Received Received
  363-P2 The human genital tubercle is steroidogenic organ at early pregnancy Iuliia Savchuk Received Received
  364-P3 Thyroid Disorders and autoimmunity in Children and Adolescents with Type 1 (T1DM) and type 2 Diabetes mellitus (T2DM) Ashraf Soliman Received Received
  364-P2 Transgender medicine is a significant part of paediatric endocrinology Ralph Decker Received Received
  365-P3 The Reference and Follow-up Signs and Symptoms of the Cases Who Are Diagnosed as Hyperthyroidism Ayla Guven Received Received
  365-P2 Prospective investigation of the the influence of triptorelin treatment on body weight and body mass index of girls who were diagnosed with idiopathic precocious puberty or early puberty. seok jin kang Received Received
  366-P3 Clinical Features in Childhood Graves Disease emine demet akba&351; Received Received
  366-P2 Genetic etiologies and gender outcomes of patients with disorders of sex development presenting with asymmetric gonads Arum Oh Received Received
  367-P3 GENERAL CHARACTERISTICS OF AUTOIMMUNE THYROID DISEASES AND EVALUATION OF ACCOMPANIED MORBIDITIS BERAY SELVER EKL&304;O&286;LU Received Received
  367-P2 A rare form of ovotesticular DSD: diagnostic and management challenges Kruthika Narayan Received Received
  368-P2 A CASE OF GONADAL DYSGENESIS DUE TO A NOVEL HOMOZYGOUS MUTATION IN NR5A2 GENE Friederike Denzer Received Received
  368-P3 Amiodarone induced hyperthyroidism in a pediatric patient Bernardo Marques Received Received
  369-P2 Assessment of initial investigation requested in adolescents with menstrual disorders MARIA CHARAMANTA Received Received
  370-P2 Persistent Mllerian Duct Syndrome in twin brothers caused by a novel mutation in the AMHR2 gene. Karolien Van De Maele Received Received
  370-P3 THYROID CARCINOMA IN CHILDREN. 7 YEARS EXPERIENCE OF A SINGLE CENTER. Cristina Preda Received Received
  371-P3 Autoimmune thyroiditis (Hashimoto thyroiditis) in a known case of autoimmune hemolytic anemia Dina Fawzy Received Received
  371-P2 Are hypospadias associated with differences in gender role behaviour and sex typical cognitive abilities? Anna Strandqvist Received Received
  372-P2 Assessment of the gonadotrophingonadal axis and Sertoli cell function in partial androgen insensitivity syndrome Doaa Khater Received Received
  374-P2 EVALUATION OF SERUM ANTI-MULLERIAN HORMONE AND ANDROSTENEDIONE LEVELS IN ADOLESCENTS GIRLS WITH MENSTRUAL IRREGULARITIES Betul Ersoy Received Received
  375-P2 Could basal AMH replace hCG stimulation test in patients with XY disorder of sex development? Shaymaa Mahfouz Received Received
  376-P3 An impressive recovery of arrested growth and puberty in a 13 year old boy after being treated for simultaneously diagnosed severe hypothyroidism and coeliac disease. Eleni panagouli Received Received
  376-P2 LONG TERM MONITORING OF GRAVES DISEASE IN CHILDREN AND ADOLESCENTS: SINGLE CENTER EXPERIENCE Selma Tun Received Received
  377-P2 Effects of Thyroid Autoimmunity on Non-Alcoholic Fatty Liver Disease in Euthyroid Girls with Hashimotos Thyroiditis Isgven Pinar Received Received
  377-P3 A Very Rare Thyroid Hormone Resistance Case Having Heterozygous Mutation in THRB Genes emel hatun aytac kaplan Received Received
  378-P3 Clinical Case (childrens endocrinology)Ieva Strauhmane Resident of child endocrinologyGunda Zvigule-Neidere - Pediatric residentIeva Kravale - Pediatric residentIveta Dzivite-Krisane, Dr.med., Assoc.prof., BKUS EndocrinologistInita Kaze - Childrens Ga Ieva Strauhmane-Brence Received Received
  378-P2 The prevalence of clinically significant anti-TPO positivity in children with HLA-conferred susceptibility to type 1 diabetes Liisa Saare Received Received
  379-P2 Encephalopathy Associated with Autoimmune Thyroid Disease: A Case Report Michael Yafi Received Received
  379-P3 Thyroid Imaging Study for the Diagnosis of Congenital Hypothyroidism with Thyroid Dysgenesis Jeesuk Yu Received Received
  380-P3 A Case of permanent congenital hypothyroidism with compound heterozygous mutations in the DUOX2 gene Jeesuk Yu Received Received
  380-P2 Celiac disease screening should be routinely offered in pediatric population with autoimmune thyroid disease Maria Resta Received Received
  381-P3 Growth catch-up on acquired hypothyroidism presenting with growth delay Joana Serra-Caetano Received Received
  381-P2 Autoimmune thyroiditis in Klippel-Feil syndrome with Arnold Chiari and syringomyelia Elisa Guidoni Received Received
  382-P3 Thyroid disease in children and adolescences with Down Syndrome 16 years of follow up in a single service Maria Claudia Schmitt-Lobe Received Received
  382-P2 Neonatal monitoring of newborns born from mothers with Graves disease. Results of a retrospective monocentric study. dominique simon Received Received
  383-P3 Corticosteroid resistant Immune Thrombocytopenic Purpura, is it a marker of future Graves Disease? María Cristina Azcona Received Received
  384-P3 Neonatal hypothyroidism following transplacental amiodarone treatment for supraventricular tachyarrhythmia. Maria Korpal-Szczyrska Received Received
  384-P2 Gravess disease during pregnancy: the impact on the fetus and the newborn Florine Belin Received Received
  385-P3 Rare case of thyroiditis De Quervain in a six-year-old girl Maria Liapi Received Received
  385-P2 Thyroid Hormone Receptor (THRB) mutation: two new cases of heterozygous mutation with significant family history James Blackburn Received Received
  386-P3 Papillary thyroid carcinoma in a 7 year old boy presenting with a goiter without microcalcifications and enlarged cervical lymph nodes Marianne Becker Received Received
  386-P2 Triac Treatment Response to Thyroid Hormone Resistantance emine demet akba&351; Received Received
  387-P2 Phenotype and genotype of four patients with thyroid hormone resistance syndrome due to mutations in the THRB gene Meropi Toumba Received Received
  387-P3 Graves disease, Methimazole and SLE-like reaction: A case report Michael Yafi Received Received
  388-P2 Clinical course in a girl with two hTPO mutations - homozygous c.1268GA (p.Gly393Arg) and heterozygous c.208CG (p.Ala70Pro): 27 years of follow up Iva Stoeva Received Received
  388-P3 A rare case of pediatric hyperthyroidism Sara Ciccone Received Received
  389-P3 AllanHerndonDudley syndrome in a patient with Global delay development a case report shahab noorian Received Received
  389-P2 A Neurological Disease Mimicking Central Hypothyroidism: MCT8 Deficiency ozgecan demirbas Received Received
  390-P2 Multinodular goiter in childhood: look for DICER1 mutation Valentine SUTEAU Received Received
  391-P2 Application of elastography in assesment of different benign thyroid lesions in children and adolescents. Hanna Borysewicz-Sa&324;czyk Received Received
  391-P3 LEVOTHYROXINE TREATMENT OF SUBCLINICAL (SH) AND OVERT (OH ) HYPOTHYROIDISM IN CHILDREN WITH AUTOIMMUNE HASHIMOTO THYROIDITIS (AHT): A RETROSPECTIVE STUDY IN REGARD WITH TSH AND FREE T4 (FT4) AT DIAGNOSIS SOFIA LEKA Received Received
  392-P2 Clinical Characteristics and Predictive Factors for the Detection of Thyroid Cancer in Children with Thyroid nodules Junghwan Suh Received Received
  392-P3 Hashitoxicosis: A rare diagnosis in childhood Stefanos Stergiotis Received Received
  393-P3 An assay led astray: a curious case of biotin-induced hyperthyroidism. Tashunka Taylor-Miller Received Received
  393-P2 THYROID NODULES IN PRADER-WILLI SYNDROME. Graziano Grugni Received Received
  394-P3 A case of steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) in a girl with newly diagnosed Hashimoto thyroiditis Yijuan Yvonne Lim Received Received
  394-P2 Early Medullary thyroid Carcinoma (MTC) in an infant with Multiple endocrine neoplasia type 2B (MEN2B, RETS Mutation codon 891) fawziya Alkhalaf Received Received
  395-P2 SERUM LEVEL OF BIOTIN RATHER THAN THE DAILY DOSE IS THEMAIN DETERMINANT OFTHEINTERFERENCE ON THYROID FUNCTION ASSAYS IN PATIENTS WITHBIOTINIDASE DEFICIENCY AHU PAKET&304; Received Received
  395-P3 Intellectual outcome at childhood in congenital hypothyroidism according to etiology and treatment related factors. Yong Hee Hong Received Received
  396-P2 THYROID FUNCTION TESTS AND AFFECTING FACTORS IN TWINS AND TRIPLETS Zeynep Atay Received Received
  397-P3 Head Circumference, Birth Length, and Weight of Neonates of Mothers with Hypothyroidism Zvi Laron Received Received
  397-P2 Hypothyroidism in a child during treatment with nivolumab for a glioblastoma. Niels Birkebaek Received Received
  398-P3 Recombinant growth hormone therapy in prepubertal children with idiopathic short stature in Korea : a phase III randomized trial Minji Im Received Received
  398-P2 Amiodarone-induced hyperthyroidism Diagnosis and clinical course in three adolescents Julia Gesing Received Received
  399-P2 Allogenic Bone Marrow Transplantation in children: Effect on thyroid function Elpis Athina Vlachoapapadopoulou Received Received
  400-P2 Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism Erdal Kurnaz Received Received
  400-P3 CLINICAL AND MOLECULAR CHARACTERIZATION OF ONE NR5A1 GENE MUTATION FOUND IN A PATIENT WITH 46, XY DSD AMAYA VELA Received Received
  401-P3 Is using a specific growth charts a chance to be more precise in evaluation the growth of the children and adolescence with Down syndrome?Comparison of the Downs syndrome growth charts with the growth charts for Polish population. Barg Ewa Received Received
  401-P2 Clinical management of childhood hyperthyroidism: A longitudinal study at a single center Tiago Jeronimo dos Santos Received Received
  402-P2 Association of Thyroid Stimulating Hormone and Free Thyroxine with Cardiometabolic Risk Factors in Euthyroid Korean Children and Adolescents Aged 10-18 years: The Korean National Health and Nutrition Examination Survey 2015 Young Suk Shim Received Received
  403-P2 Asymptomatic hyperthyrotropinaemia in children, does it correlate to true thyroid gland dysfunction? Zacharoula Karabouta Received Received
  403-P3 Epidemiology, Demographic Criteria and Risk Factors in Type 1 DM Egyptian Children: A Single Center Study Yomna Shaalan Received Received
  404-P3 Clinical and biochemical phenotype of aldosterone synthase deficiency Katharina Foertsch Received Received
  404-P2 Hearing Loss among Patients with Congenital Hypothyroidism Tal Almagor Received Received
  405-P3 Lessons from Wolfram Syndrome: Initiation of DDAVP therapy causes Renal Salt Wasting due to elevated ANP levels, rescued by fludrocortisone treatment. Kleanthis Kleanthous Received Received
  406-P3 Two siblings with Prader-Willi syndrome caused by microdeletion derived from the paternal grandmother Guanping Dong Received Received
  407-P2 Bannayan-Riley-Ruvalcaba syndrome with PTEN mutation in a patient affected by Congenital Hypothyroidism due to TPO gene alteration Maria Cristina Vigone Received Received
  407-P3 DEGLUDEC VERSUS GLARGINE IN PEDIATRIC AND ADOLESCENT PATIENTS WITH TYPE 1 DIABETES Estela Gil-Poch Received Received
  408-P3 GENETIC TESTING BY SNP ARRAY ANALYSIS IN A GROUP OF ROMANIAN PATIENTS WITH DISORDERS OF SEXUAL DEVELOPMENT Diana Miclea Received Received
  409-P3 A novel gene mutation and atypical clinical phenotype of Kallmann syndrome Yumiko Terada Received Received
  409-P2 Do Insulin like Growth Factors also influence growth in children with Congenital hypothyroidism: A cohort analysis Ruchi Goel Received Received
  410-P3 A novel detrimental homozygous mutation of WFS1 gene in two sisters from non-consanguineous parents with untreated Diabetes Insipidus Kleanthis Kleanthous Received Received
  410-P2 Study of Hearing function in children with Congenital Hypothyroidism attending Alexandria University Childrens Hospital Shaymaa Elsayed Received Received
  411-P2 Awareness of the risks of acquired iodine deficiency in strict Vegan diets Agnieszka Brandt-Varma Received Received
  412-P2 Thyroid function in the Korean obese children and adolescents: Korea National Health and Nutrition Examination Survey 2013 to 2015 JI EUN LEE Received Received
  414-P3 Is the third time really a charm? The story about three brothers suffering from adrenoleukodystrophy and about HSCT being a chance to stop the unstoppable disease. Barg Ewa Received Received
  415-P3 Case Report: Novel ACAN mutation in a SGA short stature without accelerated skeletal maturation So Eun Park Received Received
  417-P3 STUDY OF CHILDREN WITH TYPE 1 DIABETES MELLITUS OF LONG DURATION ATTENDING ALEXANDRIA UNIVERSITY CHILDRENS HOSPITAL Dina Fawzy Received Received
  418-P3 Clinical and Endocrinological Manifestations of Partial Ectopic Posterior Pituitary: A New Imaging Entity Marina Ybarra Received Received
  419-P3 A rare and unexpected cause of diabetes in childhood Supriyo Basu Received Received
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EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

57th Annual ESPE Meeting 2018

 

27 - 29 September 2018 Athens
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    ACTIVE FROM 27/09/2018 TO 27/09/2019
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                   DOI: 10.3252/pso.eu.57ESPE.2018 
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