PosterSessionOnline

EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

57th Annual ESPE Meeting 2018

27 - 29 September 2018 Athens

N. Poster

Poster title

Applicant name

Status


1-RFC14	Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer	Flora Bacopoulou	Received

1-P1	Evaluation of long term metabolic effects after prenatal dexamethasone treatment in the context of CAH - the Swedish cohort.	Lena Wallensteen	Received

1-RFC11	DIAGNOSIS AND MANAGEMENT OF PSEUDOHYPOPARATHYROIDISM AND RELATED DISORDERS: FIRST INTERNATIONAL CONSENSUS STATEMENT	Susanne Thiele-Schmitz	Received

1-RFC10	Patients with GH Insensitivity and IGF-1 Resistance Harbour Copy Number Variants Causing a Silver-Russell-Like Phenotype	Emily Cottrell	Received

1-RFC6	Allelic variation in key fitness genes is linked with increased severity of obesity in overweight/obese youth	Christoph Saner	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

1-RFC12	Use of acid-suppressivemedications during infancy and early childhood and its association with type 1 diabetes	Sruthi Menon	Received

1-RFC5	SERUM LEVELS OF THE SOLUBLE RECEPTOR FOR ADVANCED GLYCATION END PRODUCTSARE REDUCED IN CHILDREN WITH HASHIMOTOS THYROIDITIS	Tommaso Aversa	Received

1-RFC7	Next generation sequencing results in 142 patients with congenital hyperinsulinism	Diliara Gubaeva	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

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

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

1-RFC4	Metabolomic changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment	Jesús Argente	Received

2-RFC11	NATIONWIDE HYPOPHOSPHATEMIC RICKETS STUDY	SIKLAR ZEYNEP	Received

2-P1	Obesity and cardio-metabolic risk factors among Children and Adolescents with Non Classic 21-Hydroxylase Deficiency	Liat de Vries	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

2-P3	An extremely rare cause of Cushing Syndrome in chidhood	Amith Ramcharan	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

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

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

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

2-RFC6	IGF-I at 4 months associates to visceral and subcutaneous adipose tissue at 7 years of age	Emma Kjellberg	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

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

2-RFC3	Personalized and predictive medicine for pediatric diabetes through a genetic test using next generation sequencing	Valerie Schwitzgebel	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

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

2-RFC1	Changes in CYP19A1 and CYP3A4 activities due to population genetic variations in human P450 Oxidoreductase	Shaheena Parween	Received

2-RFC9	Novel variant in GNRHR gene regulatory region in a pedigree with maternally inherited precocious puberty	Magdalena Avbelj Stefanija	Received

2-P2	GnRH-analogue treatment in children with congenital adrenal hyperplasia (CAH): data from a multicenter CAH registry	Eva Hortas	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

2-RFC12	Bone mineral density is increased in 276 Danish children and adolescents with Type-1-Diabetes.	Jens Otto Broby Madsen	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

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

3-RFC12	BARRIERS AND SOURCES OF SUPPORT FOR THE PERFORMANCE OF PHYSICAL ACTIVITY IN PEDIATRIC TYPE 1 DIABETES	Michal Cohen	Received

3-RFC11	Increased levels of bone formation and resorption markers in patients with hypophosphatemic rickets.	Signe Sparre Beck-Nielsen	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

3-RFC3	Significant prevalence of severe monogenic immune defects among children with Type 1 diabetes and low T1D-genetic risk score	Stepanka Pruhova	Received

3-RFC1	Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction	Avinaash Maharaj	Received

3-P3	Nelsons syndrome after bilateral adrenalectomy for Cushings Disease in pediatric age report of a case	Catarina Machado	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

3-RFC5	Incidence and treatment outcome of childhood thyrotoxicosis	Maria Lodefalk	Received

3-RFC13	CIRCULATING MKRN3, KISSPEPTIN AND IGF-1 LEVELS IN GIRLS DURING THE CLINICAL ONSET OF PUBERTY.	Lixue Ouyang	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

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

3-RFC14	Dysregulated glucose homeostasis in Congenital Central Hypoventilation Syndrome	Yassmin Musthaffa	Received

3-RFC7	Central venous cathether-associated thrombosis in children with congenital hyperinsulinism	Daphne Yau	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

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

3-P2	Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia: a systematic Cochrane review	Sze Ng	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

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

4-RFC12	Use of telemonitoring via a mobile device app reduces HbA1c in type 1 diabetic children and adolescents	Philippe Klee	Received

4-RFC1	Mass spectrometry-based assessment of childhood androgen excess in 487 consecutive patients over 5 years	Jan Idkowiak	Received

4-RFC5	The value of cytological, histological and US examination to determine of management children with nodular goiter	Alexander Anikiev	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

4-RFC2	Novel severe skeletal dysplasia with under-mineralisation associated with reduced in utero calcium transport and TRPV6 compound heterozygous variants	Philippa Bowen	Received

4-P1	Carriers of CYP21A2 mutations have decreased mortality in infectious diseases, anational population registry study	Anna Nordenstrm	Received

4-RFC3	Functional characterization of a novel KLF11 mutation identified in a family with autoantibody-negative type 1 diabetes	Kikumi Ushijima	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

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

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

4-RFC8	Establishing age, sex, and method related reference ranges for anogenital distance - a marker of in utero androgen action	Marie Lindhardt Ljubicic	Received

4-RFC11	A new form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency caused by abolished Store-Operated Ca2 Entry	Mario Cuk	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

4-P2	Hydrocortisone (HC) dose in children with congenital adrenal hyperplasia (CAH)	Heike Hoyer-Kuhn	Received

4-RFC14	A novel germline DICER1 mutation in a girl with multinodular goiter and ovarian Sertoli-Leydig cell tumor.	katarina Gluic	Received

4-RFC6	Functionality and phenotypic characteristics of mutations in the human leptin receptor	Adriana Nunziata	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

5-RFC15	Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths	Bradley Miller	Received

5-RFC2	Identification of characteristic neurological complications in infants with Achondroplasia by routine MRI screening.	Harry Dougherty	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

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

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

5-RFC11	The Determinants Of Skeletal Fragility In Children With Type 1 Diabetes Mellitus	Suet Ching Chen	Received

5-RFC7	Alteration of Renal Corticosteroid Signaling Pathways in Preterm Infants: Neonatal Adaptation and Developmental Programming of Hypertension.	Laurence Dumeige	Received

5-RFC3	Recent changes in the pre- and postnatal growth trajectories of Offspring from Gestational Diabetic Mothers	Laurentya Olga	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

5-P2	Perioperative Care of CAH Incongruencies of Practices among Canadian Specialists	Munier Nour	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

5-RFC6	High-throughput untargeted plasma metabolomics unravels gender dimorphic metabolic trajectories in naturally conceived and ICSI prepubertal children	Alexandra Gkourogianni	Received

5-RFC12	Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes	Konstantina Mouzaki	Received

5-P1	Adrenal steroid precursors with glucocorticoid activity are able to preventadrenal crises in untreated congenital adrenal hyperplasia (CAH) patients	Manon Engels	Received

5-RFC14	Natural course of MEN type 2B syndrome; a Dutch single-center cohort.	Annemarie Verrijn Stuart	Received

5-RFC13	Pubertal voice break: Temporal relation of secondary sexual characteristics in healthy boys	Alexander Siegfried Busch	Received

5-RFC5	Evidence for a founder effect in Multiple Endocrine Neoplasia 2	Vassos Neocleous	Received

5-RFC9	Non-isolated central precocious puberty: prevalence of brain lesions and other associated disorders	Selmen Wannes	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

6-RFC5	DUOX2 Deficiency in Quebec: From Life-threatening Compressive Goiter in Infancy to Lifelong Euthyroidism	Gabrielle Dufort	Received

6-RFC2	The novel R211Q POP1 homozygous mutation causes severe short stature but uniquely only subtle skeletal dysplasia	Maha Abdulhadi-Atwan	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

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

6-P2	Analysis of phenotypes and genotypes in 84 patients with 21-hydroxylase deficiency	Lele Hou	Received

6-RFC4	Effect of 2 years of Growth Hormone Treatment on Glucose Tolerance in Adults with Prader-Willi Syndrome	Layla Damen	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

6-P3	An adrenal tumor presenting as a premature pubarche in a 7 year-old girl.	Marie-Neige CAMPAS	Received

6-LB	Sex hormone levels in young children: a pilot study of the Japan Environment and Childrens Study	Tadayuki Ayabe	Received

6-P1	Genome-wide investigation of DNA Methylation in peripheral T-cells from patients with CAH	Leif Karlsson	Received

6-RFC11	Reference Values of Automated Bone Age and Bone Health Index for Mexican children and adolescents.	América Liliana Miranda Lora	Received

6-RFC7	Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases	FLAVIA NAPOLI	Received

6-RFC9	CAN NEUROIMAGING PREDICT ENDOCRINE MORBIDITY IN CONGENITAL HYPOTHALAMO-PITUITARY (H-P) DISORDERS?	Manuela Cerbone	Received

6-RFC13	Close correlation between salivary and blood steroids in normal boys: Salivary testosterone best characterizes male puberty	Katarina Gluic	Received

6-RFC12	AMGLIDIA, a suspension of glibenclamide for patients with neonatal diabetes, long term data on efficiency and tolerance	jacques beltrand	Received

6-RFC14	Identification of epithelial sodium channel (ENaC) in endometrial pipelle biopsy samples	Aaron Hanukoglu	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

7-P2	Miscarriages in families with a child with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH)	Theresa Penger	Received

7-LB	Mutational analysis of SRD5A2 and AR genes in Indian children with 46 XY disorders of sex development	Vandana Jain	Received

7-P1	Birth Incidence, Age at diagnosis, Mortality in Congenital Adrenal Hyperplasia in Korea: A Nationwide Population-Based Study	Jihyun Kim	Received

8-P1	Impact of puberty on final height in children and adolescents with congenital adrenal hyperplasia (CAH)	Julia Rohayem	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

8-LB	Pharmacokinetics of Diazoxide Choline Controlled-Release Tablets, a Once Daily Treatment Being Evaluated in Patients with Prader Willi Syndrome	Parisa Salehi	Received

8-P3	Topical corticosteroid-induced adrenal insufficiency	Chiraz Ghaddhab	Received

9-P3	Early diagnosis of Duchenne muscular dystrophy in 6-months-old male with primary adrenal insufficiency	Eda Yanar	Received

9-LB	Two siblings with congenital syndromic hypopituitarism and TBC1D32 mutations	Johanna Hietamki	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

10-P3	LIPOID ADRENAL HYPERPLASIA DIAGNOSED WITH SEVERE CHOLESTASIS IN NEWBORN	emel hatun aytac kaplan	Received

10-LB	The influence of oil-soluble iodinated contrast medium (Lipiodol) on childs thyroid function in mice	Tadashi Hongyo	Received

10-P1	The circadian rhythm of cortisol binding globulin has little impact on cortisol exposure after hydrocortisone dosing	Richard Ross	Received

11-LB	Metabolic profile in survivors of pediatric hematopoietic stem cells transplantation after chemotherapy-only conditioning	LUMINITA-NICOLETA CIMA	Received

11-P1	Characterizing the Steroidome in Amniotic Fluid of Mid-Gestation by LC-MS/MS	Rong Wang	Received

11-P3	Severe hyponatraemia with absence of hyperkalaemia in a patient with Addisons disease	Hakan Dneray	Received

11-P2	Neonatal screening for congenital adrenal hyperplasia in Turkey: a pilot study with 38,935 infants	TULAY GURAN	Received

12-LB	Disrupting the Norm: The experience of young people with DSD	Esko Wiltshire	Received

12-P2	Autoantibodies against 21-hydroxylase in prediction of adrenal failure in APECED patients.	Leila Sozaeva	Received

12-P3	Deep bronze skin without sun exposition in a 16-year old girl	Hildegard Jasser-Nitsche	Received

12-P1	Pediatric Adrenocortical Tumors. A single tertiary center experience: Clinical, Biological and Pathologic Characteristics Analysis.	Maria Celeste Mattone	Received

13-P3	Case of primary pigmented nodular adrenocortical	Huyen Tran	Received

13-LB	Clinical and endocrine characteristics and genetic analysis of Korean children with McCuneAlbright syndrome	Minji Im	Received

13-P2	A first combination case of 21-hydroxilase deficiency and CHARGE syndrome confirmed by genetic analysis	Miyuki Kitamura	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

14-P3	Two Case Report of Adrenocortical Adenoma	Huyen Tran	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

14-P2	Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients	Melek Yildiz	Received

15-P2	Study of Cardiovascular Risk Factors and Carotid Intima-media Thickness in Children with Congenital Adrenal Hyperplasia	Shaymaa Elsayed	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

15-P1	New insights into Low Dose Dexamethasone Suppression Test in paediatric Cushings Syndrome (CS)	Ingrid Wilkinson	Received

16-LB	Successful treatment of Alopecia Totalis with calcitriol and paricalcitol in two girls aged 3 and 7-years	Eleni Dermitzaki	Received

16-P1	Recurrent hypoglycemia in a preschooler girl with overgrowth: Isolated ACTH-deficiency with a novel TPIT mutation	ZEHRA YAVAS ABALI	Received

16-P3	Adrenals and HPA axisa; Atypical presentation of adrenal insufficiency.	Khalid Khan	Received

16-P2	The spectrum of genetic defects in Congenital Adrenal Hyperplasia in the population of Cyprus: A retrospective analysis	NICOS SKORDIS	Received

17-LB	Protein-Induced Hypoglycemia Secondary to Hyperinsulinism-Hyperammonemia (HI/HA) Syndrome: a GLUD1 Gene Mutation	Fabiola DAmbrosio	Received

17-P2	Childhood Growth Advancement in Girls with Premature Adrenarche Heralds Anabolic Effects by Adulthood	Jani Liimatta	Received

17-P3	Non-classic congenital adrenal hyperplasia causing alleles among adolescent girls with PCOS genetical study.	Lasma Lidaka	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

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

18-P2	Title: A Novel Mutation in the MC2R Gene in a Two-Year-Old Boy with Adrenal Insufficiency	Katarina Gluic	Received

18-P3	Adequate interpretation of cortisol levels in children	Maria J. Chueca	Received

19-P3	ERYTHROCYTOSIS AS FIRST MANIFESTATION OF ADRENAL MASS	Mariella Valenzise	Received

19-P2	Two cases of apparent mineralocorticoid excess due to novel mutations in HSD11B2 gene	Nina Makretskaya	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

19-LB	Characterization and clinical course of prolactinoma in Korean adolescents	Minji Im	Received

20-P3	A neonatal case with Familial Glucocorticoid Deficiency Type 1 having adrenal crisis in early period	Mehmet Keskin	Received

20-LB	The efficacy and safety of octreotide treatment for diazoxide-unresponsive congenital hyperinsulinism in China	Bingyan Cao	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

20-P1	High DHEAS (HD) in girls determines earlier pubertal maturation and mild hyperandrogenism throughout pubertal development	Veronica Mericq	Received

21-P1	HIGHER DEHYDROEPIANDROSTERONE LEVELS IN PREPUBERTAL CHILDREN BORN VERY PRETERM	Veronica Mericq	Received

21-P2	Borderline peak plasma cortisol following Synacthen stimulation single-centre analysis of three years data.	Sarah Burn	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

22-P3	Identification of X-linked adrenoleukodystrophy in boys presenting with adrenal insufficiency in the absence of adrenal antibodies	Michelle Kinahan	Received

22-P2	Unilateral Adrenalectomy for primary pigmented nodular adrenocortical disease causing Cushing Syndrome	Shinji Higuchi	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

23-P2	Adrenal crisis in children with adrenal insufficiency: prevalence and risk factors	Ori Eyal	Received

23-P3	Secondary hyperaldosteronism in the course of Cystic Fibrosis	Michal Erazmus	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

24-P1	Gonadotropin-Dependent Pubertal Disorders are Common in Patients with Virilizing Adrenocortical Tumors in Childhood	Stecchini Monica	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

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

25-P3	Congenital adrenal hyperplasia due to a rare homozygous mutation R483P in the CYP21A2 gene and coexisting growth hormone deficiency	Natallia Akulevich	Received

25-P2	Very high dehydroepiandrosterone sulfate (DHEAS) in serum of an overweight female adolescent without a tumor	Daniel Iliev	Received

26-P1	Duration of breastfeeding and bone mineral density in childhood- a prospective study among preschool children	MYA THWAY TINT	Received

26-P2	Early recognition of adrenal insufficiency after hematopoietic stem cell transplantation during childhood	Yujung Choi	Received

26-P3	Rare Case of Androgen Producing Tumor in 14 Month Old Girl	Nino Kheladze	Received

27-P2	Reference values for serum 17-alfa hydroxyprogesterone and adrenal size in healthy newborns	Glay Karagzel	Received

27-P1	Bone health in adolescents born small for gestational age (SGA)	Indre Petraitiene	Received

27-P3	Adrenocortical tumours in children a case series	Rashida Farhad Vasanwala	Received

28-P2	A rare case of ACTH- independent Cushings syndrome due to bilateral micronodular adrenal hyperplasia and myoclonic dystonia	IOANNIS- ANARGYROS VASILAKIS	Received

28-P1	Longitudinal study of bone mass in Swedish children treated with modified ketogenic diet	Anna Svedlund	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

29-P1	Fracture epidemiology for children in Western Australia between 2005-2015: do we need to be concerned about bone health?	Aris Siafarikas	Received

29-P3	A New Methodology for Early Identification of Steroid Resistant Acute Graft-Versus-Host Disease Patients	Steven Ghanny	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

30-P1	Bone biochemistry in children with fractures presenting with suspected non-accidental injury	Owen Forbes	Received

30-P3	Delayed diagnosis of a patient with Antley-Bixler Syndrome	TARIK KIRKGOZ	Received

30-P2	Ganglioneuroma presenting as an adrenal incidentaloma in a 10-year-old boy-a rare entity	MEGHNA CHAWLA	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

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

32-P2	Adrenal hypoplasia seemingly first as a primary hypoaldosteronism	Silvia Ciancia	Received

32-P3	A NOVEL HOMOZYGOUS MUTATION IN THE CASR GENE IN A NEONATE WITH SEVERE PRIMARY HYPERPARATHYROIDISM ; A CASE REPORT.	Ali Alqadi	Received

32-P1	Bone mineral density and glycemic control in children and adolescents with type 1 diabetes mellitus	Gitte Fuusager	Received

33-P1	Comparison of manual and automated bone age assessment in 1285 children and adolescents aged 5 to 16 years.	Klara Maratova	Received

33-P3	A 13 Year-Old Boy Diagnosed As Osteogenesis Imperfecta With Normal Bone Mineral Density	Berna Filibeli	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

34-P1	Is Plasma C-Type Natriuretic Peptide Level Available for Typing and Diagnosis of Skeletal Dysplasia Cases?	Sukran Darcan	Received

34-P3	A rare cause of hypercalcemia in childhood: hypercalcemia associated with parathormon-related peptid	Berna Filibeli	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

35-P1	Long-term Outcomes of Osteogenesis Imperfecta in the Bisphosphonate Era	margaret zacharin	Received

36-P1	Novel LRP5 loss-of-function mutation causes Osteoporosis-pseudoglioma syndrome	Débora Braslavsky	Received

36-P2	Length estimation based on clinical and anthropometric measures in newborns.	Martha Baauregard.Paz	Received

37-P2	VITAMIN D DEFICIENT ( NUTRITIONAL) RICKETS PRESENTING IN INFANCY	Gangoda Liyanage Dilusha Chaturani Prematilake	Received

37-P3	Hypophosphatemic Hypercalciuric Ricket: 3 brothers with Dents Disease.	Claudia Godoy	Received

37-P1	Hypercalcaemia after treatment with Denosumab in children: Bisphosphonates as an option for therapy and/or prevention?	Carmen Sydlik	Received

38-P2	The Effect Of Vitamin D Receptor Polymorphism On Bone Mineral Density in Egyptian Patients With Beta Thalassemia Major	Omneya Omar	Received

38-P1	Disease Burden and Systemic Manifestations of HPP in Children Enrolled in the Global HPP Registry	Megan Cowell	Received

39-P1	3-epi-25 serum 25-hydroxyvitamin D3 concentrations in Chilean children between 5 and 8 years	Cristian Seiltgens	Received

39-P2	Vitamin D in adolescents: a comprehensive review of guidelines and recommendations	Magdalini Patseadou	Received

39-P3	Carbonic anhydrase deficiency: Three Siblings	Derya Bulus	Received

40-P3	A novel p.Gly775Glu missense COL1A2 mutation causes severe osteogenesis imperfecta in a prepubertal girl.	Eleni Kotanidou	Received

40-P2	X-Linked Hypophosphatemia Registry an international prospective patient registry	Raja Padidela	Received

40-P1	Poor metabolic control in children and adolescents with type 1 diabetes and psychiatric comorbidity	Grete Teilmann	Received

41-P2	Clinical and Biological Parameters Associated to the Severity of X-linked Hypophosphatemia in Children	Anya Rothenbuhler	Received

41-P3	SHOX gene deletion screening by FISH in children with short stature and characteristics of patients	Erdal Kurnaz	Received

41-P1	Concealment of Type 1 Diabetes in Adolescence Affects Adherence to Treatment, Metabolic Control, and Quality of Life	Judith Nir	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

42-P3	Pseudoachondroplasia	emine demet akba&351;	Received

42-P1	RISKY BEHAVIORS OF ADOLESCENTS WITH TYPE 1 DIABETES IN COMPARISON WITH THEIR HEALTHY PEERS	Betina Kandyla	Received

43-P1	The effect of social burden on paediatric diabetes outcomes	Madalena Sales-Luis	Received

43-P2	Metabolic syndrome in children with X-linked hypophosphatemic rickets (XLHR)	Anne-Sophie Lambert	Received

43-P3	LOW LEVEL OF VITAMIN D IN CHILDREN INCREASES THE RISK OF BONE FRACTURES.	Georges Nicolas	Received

44-P1	Parental anxiety about hypoglycemia of children and adolescents with type 1 diabetes mellitus (T1DM) and the associated factors.	Evangelia Ntinou	Received

44-P2	High incidence of Cranial Synostosis and Chiari Malformation in Children with X-linked Hypophosphatemic rickets	Anya Rothenbuhler	Received

44-P3	Clinical Evaluation of Eight Patients with Parathyroid Adenoma	GUL D&304;REK	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

45-P2	AN UNUSUAL CASE OF HYPOPHOSPHATEMIA IN A CHILD AFFECTED BY DI GEORGE SYNDROME	Mila Kalapurackal	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

46-P2	Novel SLC34A1 mutation in a girl infant with idiopathic infantile hypercalcemia	seok jin kang	Received

46-P1	Phenotypes of diabetes and determinants of glycemic control and diabetes complications in Haitian youth living in Haiti	Marie-Pier Dumas	Received

47-P2	A Novel Variant of SLC34A1 Gene in an Infant with Idiopathic Infantile Hypercalcemia	Gi-Min Lee	Received

47-P3	Evaluation of Bone Mineral Density and Bone Metabolism Markers in Children Diagnosed as Celiac Disease	Havva Nur Peltek Kendirci	Received

47-P1	SMOKE EXPOSURE AND CARDIO-METABOLIC PROFILE IN YOUTH WITH TYPE 1 DIABETES	Valeria Calcaterra	Received

48-P2	Infantile Arterial Calcification and Subsequent Hypophosphatemia Due to ENPP1 mutation A case followed through to adulthood	Munier Nour	Received

48-P1	Menstrual cycle disorders in young women with type 1 diabetes mellitus	Ioanna Kosteria	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

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

49-P2	Pediatric Quality Of Life Inventory In Children With Osteogenesis Imperfect In Dr Soetomo Hospital Surabaya	nur rochmah	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

50-P2	Osteoporosis-pseudoglioma Syndrome (OPPG): Improvement of Osteoporosis on Biphosphonate Therapy	Esin Karakilic-Ozturan	Received

50-P3	Hypocalcemia secondary to maternal vitamin D deficiency	Khalid Khan	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

52-P3	A rare case of familial hypocalcemia.	Leila Sozaeva	Received

52-P1	Genetic susceptibility to Type 1 Diabetes in children: analysis of polymorphisms rs1990760 - IFIH1, rs20541 - IL13 , rs231775 - CTLA 4	Aleksandra Goralczyk	Received

52-P2	Evaluation of bone mineral density in a cohort of children with Growth Hormone deficiency	Valentina Cenciarelli	Received

53-P1	Neonatal diabetes as a first symptom of IPEX syndrom	Agnieszka Brandt-Varma	Received

53-P3	HDR Syndrome: A Case Report of Hypoparathyroidism, Hearing Loss and Renal Agenesis	Mihaela Dimitrova-Mladenova	Received

53-P2	Follow-up on bone health in children with acute lymphoblastic leukemia (ALL)	Hamilton Cassinelli	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

54-P3	Growth in the coeliac disease of the child	Mimouna Bessahraoui	Received

54-P2	Effect of Pubertal inductionn bone mass accrual, in adolescent boys with Duchenne muscular dystrophy	Margaret Zacharin	Received

55-P3	The British OsteoNEcrosis Study: A Multi-Centre Prospective Study	Nadia Amin	Received

55-P1	Wolfram Syndrome case with hypergonadotropic hypogonadism: A novel mutation	ZEYNEP UZAN TATLI	Received

56-P3	Response to pamidronate therapy and pharmacogenetics in patients with Osteogenesis Imperfecta	Nalini M Selveindran	Received

56-P2	First reported cases of a novel variant of GNAS 1 gene	Argyro Panagiotakou	Received

56-P1	Different Clinical Findings in Maturity Onset Diabetes of The Young due to B-Lymphocyte Kinase Gene Mutations	Ayla Guven	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

57-P2	AN UNUSUAL CAUSE OF SHORT STATURE	Serap Turan	Received

57-P3	Results of 22 weeks of burosumab therapy in a patient with severe bone deformities due to XLH	Pablo Ruiz-Ocaña	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

58-P3	Severe neonatal hypercalcemia: a challenging case	Raihana Hashim	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

59-P2	Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism	emine demet akba&351;	Received

59-P1	Impact of diabetes during pregnancy in women affected with GCK-MODY on neonatal health outcome.	Agnieszka Brandt-Varma	Received

59-P3	Assessment of Vitamin D Status in Healthy Pre-pubertal Egyptian Children	Rasha Hamza	Received

60-P3	Are Caucasian children at risk of sub-optimal vitamin D levels?	Krutika Shrikhande	Received

60-P2	Incidence of Childhood Type 1 and Type 2 Diabetes Mellitus in Qatar between 2012- 2016	ASHRAF TAWFIK SOLIMAN	Received

61-P3	Incidence of vitamin D deficiency in 12-year old children in Japan	Satomi Koyama	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

61-P2	The Prevalence of Double Diabetes in Children and Adolescents in Qatar	Ashraf Soliman	Received

62-P3	Idiopathic Juvenile Osteoporosis: Common Symptoms in an Uncommon Condition	SAURABH UPPAL	Received

62-P2	Prevalence of Diabetes Type 1 and type 2 in children and adults in Kazakhstan in 2016	Akmaral Nurbekova	Received

63-P1	Glucose Intolerance in Survivors of Childhood Hematologic Disorders	Seonhwa Lee	Received

63-P2	Detection of the pathogenic genes in the diagnosis and treatment of hyperglycemia infants and children	Zhuhui Zhao	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

64-P2	Early diagnosis of diabetes type 2 in children with progeria syndromes	Martin Bald	Received

65-P1	Evaluation of Diabetes Related complications and Endothelial dysfunction in Adolescents with Type 1 Diabetes	Nehad Metwally	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

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

66-P3	A case of Turner syndrome with Graves disease and primary hyperparathyroidism	Shigeru Nagaki	Received

66-P1	Complexities in the management of New-Onset Diabetes After Transplantation (NODAT) in an adolescent with Senior-Loken syndrome	Philippa Bowen	Received

67-P2	Pathogenetic heterogeneity of diabetes mellitus in children of Saint-Petersburg city.	Mariia Turkunova	Received

67-P1	INSULIN RESISTANCE PARAMETERS IN CHILDREN WHO WERE BORN VERY PRETERM AND ADEQUATE FOR GESTATIONAL AGE	Hernan Garcia	Received

67-P3	Neonatal hypocalcemia revealing a malignant osteopetrosis.	Valérie Porquet-Bordes	Received

68-P3	Frontal behavior dysfunctions revealing a dramatic progression of complex cranial base abnormalities in a severe osteogenesis imperfecta.	Valérie Porquet-Bordes	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

69-P1	Triglyceride glucose index as a predictor of impaired glucose tolerance in overweight and obese adolescents	Voraluck Phatarakijnirund	Received

69-P3	Ionized calcium and 25-hydroxyvitamin D3 in children with steroid-sensitive nephrotic syndrome.	Yasmine Abdelmeguid	Received

69-P2	Features of Japanese patients with early-onset, MODY-like diabetes without mutations in the major MODY genes.	Tohru Yorifuji	Received

70-P1	Birth weight in offsprings of mothers with gestational diabetes mellitus due to mutations in GCK gene.	Natalia Zubkova	Received

70-P2	Frequency and etiologic spectrum of monogenic diabetes in pediatric diabetes in a single academic center	Jin-Ho Choi	Received

70-P3	Hypercalcemia due to six newly identified inactivating mutations in the CaSR gene	Y&305;lmaz Kor	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

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

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

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

73-P3	Effects of Diabetes mellitus Type--1..on vitamin D status amomng children ....	Katarina Gluic	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

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

74-P2	The application of Next Generation Sequencing MODY Gene Panel in Greek Patients	Elizabeth Tatsi	Received

74-P1	Catheter site ion and anthropometric measurements at subjects with type 1 diabetes and continuous subcutaneous insulin infusion	Maria Xatzipsalti	Received

74-P3	Association between prior Toxic Stressors and development of T2DM in Adolescents	Adam Adamidis	Received

75-P1	OPEN SOURCE ARTIFICIAL PANCREAS SYSTEMS USED FROM BULGARIAN CHILDREN AND YOUNG PEOPLE WITH DIABETES	Maia Konstantinova	Received

75-P3	First 4 cases of neonatal diabetes from Kazakhstan, Almaty with proven mutations in KCNJ11 and INS genes	Akmaral Nurbekova	Received

75-P2	TYPE 5 MONOGENIC DIABETES: REPORT OF 7 CASES.	Eduard Mogas Viñals	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

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

76-P1	National Survey of usage of continuous glucose monitoring in children and adolescents at non reimbursed setting	Yuliya Bazdarska	Received

77-P2	Clinical and Genetic Characterizations of Maturity Onset Diabetes of The Young: Single Center Results	Ayla Guven	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

78-P2	Protein and fat effects on post - prandial glucose responses among Egyptian children and adolescents with Type 1 diabetes mellitus	Noha Arafa	Received

79-P1	A Novel SLCA16A1 mutation in An Infant with Hypoglycemia and Severe Metabolic Ketoacidosis.	Reem Hasnah	Received

79-P2	Amino acids plasma profile in children with type 1 diabetes	Teodoro Durá-Travé	Received

80-P2	Betatrophin as a new biomarker of Type 1 Diabetes Mellitus in Paediatrics	Laura Bosch i Ara	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

80-P3	Clinical and Biochemical Characteristics of Familial Type 1 Diabetes Mellitus (FT1DM) compared to Non-Familial Type 1 DM (T1DM).	ashraf soliman	Received

81-P2	Vitamin D status among lraqi children and adolescent with T1DM	Mohamed AlAbadi	Received

81-P1	ZFP57-associated transient neonatal diabetes is responsive to oral sulfonylurea treatment	Christina Reinauer	Received

82-P2	IGF-1 relationship with growth velocity in precocious puberty with GnRHa treatment	nursel muratoglu sahin	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

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

83-P3	Real world clinical evolution of type 1 diabetes patients on twentyyears	Beatriz Garcia Cuartero	Received

83-P2	Relation between hypomagnesemia and increased level of HbA1c in patients with diabetes mellitus	seok jin kang	Received

83-P1	HERV-W-Env protein expression in pediatric type 1 diabetes patients	Michael Hauschild	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

84-P3	Diabetic capilaropathy: a case report	Carlos Andrés	Received

84-P2	PID1 alters antilipolytic action of insulin and increases lipolysis via Inhibited the activation of AKT/PKA Pathway	chunyan yin	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

85-P1	T and B-Lymphocytes Levels in Children with Type 1 Diabetes in association with Candida infection	Stanimira Elkina	Received

85-P3	A sibling case of Wolfram syndrome with diabetes mellitus diagnosed within 10 months in early childhood	DAI SUZUKI	Received

86-P1	Coincidence of Newly Diagnosed Type 1 Diabetes Mellitus with Enteroviruses and Respiratory Tract Viruses	Murat Karaoglan	Received

86-P3	Continuous Subcutaneous Insulin Infusion in Children and Adolescents:Analysis of Initial and Follow up Basal Rates	Damla Gk&351;en	Received

87-P1	Investigation into -cell adaptation during puberty	Anne-Laure Castell	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

87-P2	Translating the A1C Assay into Estimated Average Glucose Values in Children with Type 1 Diabetes Mellitus	Ashraf Soliman	Received

88-P2	Relationship between residual endogenous insulin secretion and glycemic control in Japanese children and adolescents with type 1 diabetes.	Ikuma Musha	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

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

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

89-P1	FEATURES OF T2DM IN ADOLESCENTS WITH LOW TITER OF ICA AND IAA	Irina Eremina	Received

89-P2	A Curious Case of Persistent Lactic Acidosis in a Child with Diabetic Ketoacidosis	Andrew Sng	Received

90-P2	An unusual case of an exclusively vegan child with diabetic acidosis	Maria Xatzipsalti	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

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

91-P1	Screening for T2D in high risk Egyptian children and adolescents using strip HbA1c and OGTT	Noha Musa	Received

91-P3	Clinical and Epidemiological Features of Children with Type 1 Diabetes	emine demet akba&351;	Received

92-P2	Hypertriglyceridemia in Type 1 Diabetes children during Diabetic Ketoacidosis; Relation to DKA severity and Glycemic control.	Noha Musa	Received

92-P3	Predictors of Optimal Glycemic Control in Children with Diabetes Mellitus Type 1 Receiving Pump Insulin Therapy.	Evgeniya Evsyukova	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

93-P2	Acute mononeuropathy in an 8-year-old-girl with newly diagnosed type 1 diabetes	Styliani Giza	Received

93-P3	Symptomatic cerebral infarction: A Rare Complication of Diabetic Ketoacidosis	Gamze Celmeli	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

94-P3	OUR CLINICAL EXPERIENCES IN TYPE 2 DIABETES	gl direk	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

94-P2	HLA- G gene promoter methylation status in children and adolescents with Type 1 Diabetes	Konstantina Mouzaki	Received

95-P2	Impaired adrenal function in pediatric patients with Diabetes Mellitus type 1 evaluated with low-dose Synacthen test	MARIALENA KALYMNIOU	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

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

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

96-P1	KISSPEPTIN AND THE GENETIC OBESIDOME	STYLIANI GERONIKOLOU	Received

96-P3	Serum trace element levels in children presenting with diabetic ketozis and diabetic ketoacidosis: A longitudinal controlled study	Hakan Dneray	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

97-P2	Higher percentage of insulin pump users at Isle of Man (IOM) Two years observational data	Arundoss Gangadharan	Received

97-P1	Circulating Exosomal miRNAs Involved in the Pathogenesis of Children Nonalcoholic Steatohepatitis	Xuelian Zhou	Received

98-P3	A CASE OF CHILDHOOD TYPE 1 DIABETES MELLITUS WHO DEVELOPED GRANULOMA ANNULARE	Havva Nur Kendirci	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

98-P1	PLACENTAL FATTY ACID PROFILE, DNA METHYLATION AND ADVERSE METABOLIC OUTCOMES IN THE OFFSPRING AT SCHOOL AGE	Abel Lopez-Bermejo	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

99-P3	CASE REPORT: DE NOVO MUTATION OF FOXP3 CAUSING MILD PHENOTYPE OF IMMUNODYSREGULATION, POLYENDOCRINOPATHY, ENTEROPATHY, X-LINK SYNDROME	HOANG THI DIEM THUY	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

100-P1	Serum catestatin levels in obese children and adolescents	Marko Simunovic	Received

100-P2	The glycemic variability in children with diabetes mellitus	Oleg Dianov	Received

100-P3	Is there a relationship between Immune-mediated Type 1 Diabetes Mellitus and Congenital Rubella Infection?	Huseyin Anil Korkmaz	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

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

101-P1	Circulating MOTS-c levels are decreased in obese male children and adolescents and associated with insulin resistance.	Caiqi Du	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

102-P1	Plasma adropin levels are associated with lipid characteristics amongst children with obesity	Ruimin Chen	Received

102-P3	WHEN TYPE MODY II DIABETES SIMULATES TYPE I DIABETES	IRENE PILAR FERNANDEZ VISERAS	Received

103-P2	Donohue syndrome With Hypertrophic Cardiomyopathy	Derya Bulus	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

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

105-P1	Effect of a Melanocortin-4 Receptor (MC4R) Agonist, Setmelanotide, on Obesity and Hyperphagia in Individuals Affected by Alstrm Syndrome	Katie Fleming	Received

105-P2	Post-prandial hyperinsulinaemic hypoglycaemia after oesophageal surgery in children	Antonia Dastamani	Received

105-P3	MONOGENIC DIABETES CAUSE BY MUTATION OF THE GENE HNF1A	Juan Manuel Narvaez Echeverri	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

106-P3	REVERSIBILITY OF EARLY ACUTE DIABETIC NEUROPATHY (DN) IN ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS (T1D)	Maria Louraki	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

107-P1	Serum uric acid level and its association with metabolic syndrome in Korean adolescents	So Yoon Jung	Received

107-P2	Congenital Hyperinsulinism in a child with Alagille Syndrome	Antonia Dastamani	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

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

108-P2	Severe stress-induced insulin resistance in an eight year old boy with T1DM, reversed after psychiatric treatment	Christi van Ommen	Received

109-P2	A case of neonatal diabetes due to pancreatic hypoplasia	Zacharoula Karabouta	Received

109-P1	EFFICIENCY OF ALPHA-LIPOIC ACID IN METABOLIC SYNDROME TREATMENT IN CHILDREN	Olena Tolstikova	Received

110-P3	Diabetes Mellitus, Autoimmune Hemolytic Anemia, Hepatosplenomegaly and Lymphadenopathy: a Rare Association in Chinese Children	Miaoying Zhang	Received

110-P2	Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins	Shira London	Received

110-P1	Lipid accumulation product is a predictor of non-alcoholic fatty liver disease in childhood obesity	Bahar Ozcabi	Received

111-P1	Selected serum adipokines in children with irritable bowel syndrome	Joanna Oswiecimska	Received

111-P3	Type 1 diabetes and central precocious puberty a rare association	Mimouna Bessahraoui	Received

112-P1	Role of urinary NGAL and KIM-1 as early kidney injury biomarkers in obese prepubertal children	Francesco Chiarelli	Received

112-P3	DIABETIC KETOACIDOSIS AMONG EGYPTIAN CHILDREN WITH TYPE 1 DIABETES: 3-YEARS STUDY	Mona Karem	Received

112-P2	A RARE CASE OF DIABETES MELLITUS TYPE 1 IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1	ELENI PANOUTSOU	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

113-P3	Fructosamine Level In Type 1 Diabetes Mellitus Children Performing Ramadhan Fasting	nur rochmah	Received

114-P1	Intrauterine metformin exposure and offspring metabolic health at 8-years follow-up	Liv Guro Engen Hanem	Received

114-P2	Gender characteristics of responsibility for their own health of adolescents with type I diabetes mellitus	Svitlana Chumak	Received

114-P3	Metformin Therapy in A lean Adolescent girl with prediabetes dysglycemia treated: Good Response.	ashraf soliman	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

115-P2	Favorable outcome despite prolonged hypoglycemic episodes following a massive insulin overdose: a case series	Heike Vollbach	Received

115-P3	Association Between Thyroid Stimulating Hormone and Hemoglobine A1c in Type 1 Diabetes Mellitus Children	nur rochmah	Received

116-P1	Rapid BMI gain during later infant accelerates skeletal maturation at prepubertal obese children	Toru Kikuchi	Received

116-P2	The Effect of a Reduced Fluid Replacement Regimen on the Resolution of DiabeticKetoacidosis (DKA) in Children	Danica Shanee Hapuarachchi	Received

116-P3	Monogenic Diabetes in 2 Years and 4 Months Old Girl: Is it DEND?	nur rochmah	Received

117-P1	The more obese -the less pubertal height gain	Anton Holmgren	Received

117-P2	Prevalence of and Risk Factors for Nonadherence to Insulin among Paediatric Type 1 Diabetes Patients in Singapore	Brandon Chua	Received

117-P3	Compliance for monitoring of glycemic control in children with type 1 diabetes	Oleg Latyshev	Received

118-P3	Ketogenic Diet in a child with Diabetes and Global developmental delay	Myat Win	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

118-P1	LONGITUDINAL CHANGES IN ABDOMINAL FAT DISTRIBUTION IN THE FIRST TWO YEARS OF LIFE	Inge van Beijsterveldt	Received

119-P1	Telemedicine Therapy for Overweight Adolescents: First Results of a Novel Smartphone App Intervention using a Behavioural Health Platform	Katrin Heldt	Received

119-P2	Parental Knowledge and Attitudes toward Diabetes Mellitus type 1: a cross sectional study	Norah Albanyan	Received

120-P1	Cardiorespiratory fitness effectiveness is related to abdominal adiposity and insulin sensitivity in overweight adolescents	Tetyana Chaychenko	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

121-P3	Pediatric stroke as the presenting symptom of new onset diabetes without DKA	Sonum Bharill	Received

121-P1	Promoting Healthy Lifestyles in Youth: Preliminary Findings from the CIRCUIT Program	Marina Ybarra	Received

122-P1	Determinants of Attrition from a Healthy Lifestyle Intervention: Experience from the CIRCUIT Program	Marina Ybarra	Received

122-P3	Challenges In Educating New Onset Type 1 Diabetes MellitusPatients: Can The Use Of a Tablet Be The Answer?	Steven Ghanny	Received

122-P2	A Young Type 1 Diabetic with Acute Hemichorea: Rare central nervous system complications	Andrew Sng	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

123-P2	Allopurinol Ameliorates Non-alcoholic Fatty Liver Disease in Rats	Huseyin Anil Korkmaz	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

124-P3	Continuous glucose monitoring results of our cases with MODY type 2 diabetes	ZEYNEP UZAN TATLI	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

125-P2	Angiotensin- Converting Enzyme Insertion/Deletion Gene Polymorphism in Egyptian Obese Children and Adolescents: Relation to Hypertension Risk	Rasha Hamza	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

126-P2	Serum calprotectin level in children: marker of obesity and its metabolic complications.	Valeria Calcaterra	Received

126-P1	Effect of hormonal changes on exocrine pancreatic function in girls with anorexia nervosa	Ma&322;gorzata Stojewska	Received

127-P1	PCSK9 and Lp(a) levels of children born after ?ssisted Reproduction Technologies	Ioanna Kosteria	Received

127-P3	BigO: Big Data Against Childhood Obesity	Anastasios Delopoulos	Received

127-P2	Pediatric Continuous Metabolic Syndrome Score (PsiMS score): Use in Everyday Clinical Practice	Rade Vukovic	Received

128-P3	Exposure to bisphenol-A and phtalates in obese girls	annalisa deodati	Received

128-P1	Rate of accumulation of abdominal fat is associated with fasting glucose levels in early childhood	Suresh Anand Sadananthan	Received

128-P2	LEPTIN AND CYTOKINES ARE NOT THE BEST MARKERS FOR METABOLIC S.	Beatriz Garcia Cuartero	Received

129-P1	Early menarche is associated with insulin resistance and non-alcoholic fatty liver disease in obese adolescents	ANNA DI SESSA	Received

129-P2	Early-life risk factors and their association with hypertension in Spanish children and adolescents	Gloria Bueno-Lozano	Received

129-P3	OBESITY OF CHILDHOOD and AMBULATORY GLUCOSE MONITORIZATION	Aya Trel Ergr	Received

130-P3	Familial Partial Lipodystrophy, Importance of family history - a case report	Camilla Stockley	Received

130-P1	The frequency of obstructive sleep apnea in children with hypothalamic and exogenous obesity	DICLE CANORUC	Received

130-P2	A rare case of diabetes mellitus in an adolescent: partial lipodystrophy	Samim zen	Received

131-P1	THE IMPORTANCE OF UNIVERSAL LIPID PROFILE SCREENING IN TWO TO TEN YEARS OLD LEBANESE CHILDREN.	Georges Nicolas	Received

131-P2	Visfatin, RBP4 and STRA6 polymorphisms in relation with childhood obesity	Ionela Pascanu	Received

131-P3	Development of severe obesity in a child with a brainstem tumor	Catherine Pihoker	Received

132-P2	CHARACTERISTICS OF BLOOD LIPIDS IN BOYS WITH HYPOANDROGENIA	Olena Budreiko	Received

132-P3	CORRELATION BETWEEN OBESITY, BODY MASS INDEX AND INSULIN RESISTANCE IN BULGARIAN CHILDREN	Desislava Yordanova	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

133-P3	Nonclassical manifestation of PWS	Elena Bogova	Received

133-P2	Tri-Ponderal Mass Index. A good anthropometric index to evaluate adiposity in children and adolescents.	Miguel Klnder	Received

133-P1	Severe Obesity and Cardiometabolic Comorbidities in Adolescents: Chronology of an Epidemic	Orit Pinhas-Hamiel	Received

134-P3	Metabolic parameters in children with syndromic obesity	Elena Sukarova-Angelovska	Received

134-P2	Serum Spexin Concentrations in Adolescent Females with Metabolic Syndrome, Polycystic Ovary Syndrome and Anorexia Nervosa	FLORA BACOPOULOU	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

135-P3	Cut-off for the follow-up of obese children: cynicism or realism?	Francesco Gallo	Received

135-P2	A SIMPLE RELAXATION EXERCISE REDUCES STRESS IN OBESE YOUTH - A PATH TO A HEALTHY LIFESTYLE?	Aikaterini Stasinaki	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

136-P2	Dyslipidemia and Its Related Factors in Chinese Children and Adolescents with Turner Syndrome	Siqi Huang	Received

136-P3	PROXIMAL MICRODELECTION 16p11.2 SYNDROME	Francesco Leo	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

137-P2	Severity, duration and phenotype of obesity promote precocious cardiovascular sonographic alterations in childhood obesity.	Domenico Corica	Received

137-P1	NEONATAL SCREENING TESTS IN PREMATURE NEWBORNS IN SOUTHERN BRASIL	Suzana Nesi-Frana	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

138-P3	A compound heterozygote mutation in a Chinese patient affected with Methylmalonic acidemia	HUI HUANG	Received

138-P2	Physical activity determined by accelerometry before and after an integral treatment program in children with abdominal obesity	María Cristina Azcona	Received

139-P1	Transient neonatal iatrogenic hypothyroidism due to iodinated contrast	Ulrika Hrenstam	Received

139-P3	LYMPOSOMAL ACID LIPASE DEFICIT IN PATIENTS WITH HYPERCHOLESTEROLEMIA	Ignacio Diez	Received

140-P2	Sex-related differences and effect of puberty on Metabolic Syndrome in obese children and adolescents	Chiara Guzzetti	Received

140-P1	SEXUAL DIMORPHISM OF IGF1 AND IGF2 EXPRESSION IN THE NEONATAL RAT BRAIN	Julie Chowen	Received

140-P3	HEPATIC STEATOSIS AND ITS RELATIONSHIP WITH THE METABOLIC SYNDROME	IRENE PILAR FERNANDEZ VISERAS	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

141-P3	Serum hepcidin and ferritin in prepubertal obese children	Joanna Gajewska	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

142-P3	Osse Registry for Patients with Lipodystrophy run by the European Consortium of Lipodystrophy (ECLip)	Julia von Schnurbein	Received

142-P2	Children with obesity are taller in early childhood with subsequent catch-down growth until adolescence	Elena Kempf	Received

142-P1	GROWTH HORMONE DEFICIENCY DUE TO WHOLE-GENE DELETION OF GHRHR	Sezer Acar	Received

143-P1	Severe pre- and postnatal growth retardation in a child harboring a novel homozygous IGF1 gene mutation.	Ana Claudia Keselman	Received

143-P3	Acanthosis nigricans in obese children and adolescents in relation to severity of obesity and insulin resistance.	Kyung Hee Park	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

144-P3	Serum uric acid and its correlation with metabolic syndrome factors in simple obesity children	ZULIN LIU	Received

144-P2	Efficacy, safety and tolerability of Liraglutide, GLP-1 Analogue, in Indian adolescent population with obesity	Inderpal Kochar	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

145-P3	Thyroid function, lipid profile and carbohydrate metabolism parameters in patients with Alstrom syndrome.	Maja Oko&324;ska	Received

145-P1	Response to growth hormone in patients with isolated familial growth hormone deficiency due to RNPC3 mutations	Gabriel Á. Martos-Moreno	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

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

146-P1	Laron syndrome patients have an abnormal plasma amino acid pattern	Laron Zvi	Received

147-P3	Bariatric surgery as treatment of primary Pseudotumor cerebri in a male adolescent: case report	Marina Ybarra	Received

147-P2	Relation between cardiac function and anthropometric parameters in overweight and obese school boys	Viktoriya Furdela	Received

147-P1	Serum IGFBP-2 concentration in neonates with potential diagnosis of growth hormone deficiency (GHD).	MARIA GABRIELA BALLERINI	Received

148-P3	Investigation of Pubertal Effect on Thyroid Volume and IGF-1 Changes in Morbid Obese Children	Murat Karaoglan	Received

148-P2	EVALUATION OF HYDRATION STATUS OF OBESE CHILDREN- A PILOT STUDY	Ayse Nurcan Cebeci	Received

149-P2	GALANIN IS POSITIVELY CORRELATED WITH INSULIN RESISTANCE AND TRIGLYCERIDE LEVELS IN OBESE CHILDREN	Sezer Acar	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

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

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

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

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

151-P3	LIPIDOGRAM, LEPTIN-AND ADIPONECTINAEMIA IN TEENAGERS AND ADOLESCENTS WITH METABOLIC SYNDROM	Olena Tolstikova	Received

152-P3	Metabolic Endotoxemia in Egyptian Obese Children And Adolescents	Omneya Omar	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

152-P1	MICROALBUMINURIA AND GLOMERULAR FILTRATION RATE IN SGA BORN YOUNG ADULTS	Wesley Goedegebuure	Received

153-P2	Early BMI Trajectory Classes are Linked to Distinct Body Fat Partitioning Later in Childhood	Navin Michael	Received

153-P3	Resting metabolic rate and the development of metabolic disorders in obese children	Pavel Okorokov	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

154-P1	Early onset GH replacement in GH deficiency: Is neonatal hypoglycemia important for long term follow-up?	Dicle EMET	Received

154-P2	Hair Cortisol Concentrations in Overweight and Obese Children and Adolescents	Sofia Genitsaridi	Received

154-P3	Relation Of Screen-Time(Phone-Computer-TV-Online Games) And Physical Activity With Childhood Obesity	Mehmet mustafa YILMAZ	Received

155-P2	Associations between body fat mass and internalizing and externalizing behaviors and anxiety in children and adolescents	Eirini Christaki	Received

155-P3	Effect of three-month diet and physical activity on adipokines and inflammatory status in children with metabolic syndrome	Ramona Stroescu	Received

155-P1	Prevalence of diabetes among children treated with growth hormone in Israel	Zvi Laron	Received

156-P2	Pharmacotherapy and the effects on LDL levels and growth in 2 children with severe Familial Hypercholesterolemia	Aravind Venkatesh Sreedharan	Received

156-P3	NECK CIRCUMFERENCE AND LIPID PROFILE IN ADOLESCENTS WITH OVERWEIGHT / OBESITY	Ricardo Arrais	Received

156-P1	The effect of growth hormone treatment in children after hematopoietic stem cell transplantation	Sabine Hannema	Received

157-P3	A not so simple obesity	Silvia Poluzzi	Received

157-P1	Easypod Connect Observational Study: The Italian Experience	Giovanna Orlando	Received

157-P2	Brown tumors in children on hemodialysis	russka shumnalieva	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

158-P2	The role of fibroblast growth factor 21 and irisin in the pathogenesis of obesity in childhood and adolescence	Sofia-Iliada Karampatsou	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

159-P2	Serum NAMPT levels are not associated with parameters of liver function in children and adolescents	Antje Garten	Received

159-P3	COMPLIANCE OF OBESE CHILDREN AND THEIR FAMILY TO THE DIRECTIONS OF A PEDIATRIC ENDOCRINOLOGY MEDICAL OFFICE	Sotiria Giannopoulou	Received

160-P2	Obesogenic environment and its influence on adiposity on Mexican children and adolescents.	América Miranda_Lora	Received

160-P3	RISK FACTORS AND COMORBIDITIES OF CHILDHOOD OBESITY	Sotiria Giannopoulou	Received

161-P3	AUTONOMIC NERVOUS SYSTEM -INFLAMMATION LINK: A NEW INDEPENDENT MECHANISM FOR HOMEOSTASIS	STYLIANI GERONIKOLOU	Received

161-P2	Metabolic alterations and weight status in children at 8 years: a prospective cohort study	ISOLINA RIAÑO-GALAN	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

162-P2	Correlation of dietary habits with systolic blood pressure in healthy children	Maria Efthymia Katsa	Received

162-P3	Effects of a brief Physician delivered counseling on childhood obesity	SUNETRA MONDAL	Received

163-P2	Evaluation of voiding dysfunction in obese children	bayram ozhan	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

164-P1	Changing patterns of growth in Prader-Willi syndrome	Georgia Irene Neophytou	Received

164-P2	Comparison of antropometric and biochemical parameters in obese children with or without primary headache	onur AKIN	Received

165-P2	The protective effect of exclusive breastfeeding for overweight/ obesity in children with high birth weight	Hae Soon Kim	Received

166-P2	Determinants and consequences of exaggerated adrenarche in simple obesity.	Jean De Schepper	Received

166-P3	Assessment of obesity in children with achondroplasia and hypochondroplasia	Yukako Nakano	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

167-P1	Improved mental and motor development during 3 years of GH treatment in very young children with Prader-Willi syndrome	Stephany Donze	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

167-P2	Metabolic alteration in Patients affected by PseudoHypoParathyroidismo 1a (PHP1a): a preliminary data	Danilo Fintini	Received

168-P2	Weight loss outcomes in two-year multidisciplinary lifestyle intervention program involving obese children and their parents	Katja Dumic Kubat	Received

168-P1	GH response to GHRH and Arginine in previously GH-treated young adults with Prader-Willi syndrome	Stephany Donze	Received

168-P3	Beneficial effect of metformin treatment in obese children and adolescents	Zdravka Todorova	Received

169-P1	A novel type of Pubertal Height, Weight, and BMI Reference, aligned for Onset of Puberty.	Anton Holmgren	Received

169-P2	Relationship between glucose and lipid metabolism, inflammatory factors and adipokines in children with obesity	Ruimin Chen	Received

170-P1	Evaluating cut-offs for automatic growth screening in Swedish children using the Finnish growth monitoring algorithm	Lars Gelander	Received

170-P2	Development of resistance to Sorafenib, a multikinase inhibitor, in hepatocellular carcinoma is mediated by SIRT	Antje Garten	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

171-P3	COMPARISON OF METABOLIC PARAMETERS OF OFFSPRINGS BLOOD DEPENDING ON THE LEVEL OF GLYCEMIA DURING PREGNANCY	Alisa Masel	Received

171-P1	Prospective study of growth in Swedish children treated with modified ketogenic diet	Anna Svedlund	Received

172-P2	Iron metabolism disorders in prepubertal obese children with and without NAFLD	Francesco Chiarelli	Received

172-P1	Early Gut Mycobiota and Childhood Growth	Kasper Schei	Received

172-P3	Forty patients with persistent, non-focal congenital hyperinsulinism: Urgent need for new treatment modalities	Amalie Greve Rasmussen	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

173-P2	Familial hypercholesterolemia due to homozygous LDLRAP1 mutation: variability of phenotype and response to medical therapy.	Evangelia Panou	Received

173-P1	Clinical and radiological manifestations in a large Swedish family with a pathogenic heterozygous ACAN variant	Alexandra Gkourogianni	Received

174-P2	CAN TRIPONDERAL MASS INDEX BE A NEW INDICATOR IN THE PREDICTING CARDIOMETABOLIC RISK IN OBESE ADOLESCENTS?	Berna Filibeli	Received

174-P1	IDENTIFICATION OF ADAMTS6 AS A NOVEL CANDIDATE GENE FOR IDIOPATHIC SHORT STATURE WITH ADVANCED BONE MATURATION	Diana Monica Warman	Received

175-P2	Social Networks, Social Support and Weight-Related Outcomes among Adolescents	Marina Ybarra	Received

175-P3	NEONATAL DIABETES MELLITUS IN VIETNAM NATIONAL CHILDREN HOSPITAL	Ngoc Can Thi Bich	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

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

176-P2	Identification of A Novel Homozygous Mutation in BBS10 in Five Children With Bardet-Biedl Syndrome	glay can y&305;lmaz	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

177-P2	THE EFFECTS OF THE BIRTH WEIGHT ON THE FAT DISTRIBUTION AND FATNESS PARAMETERS OF THE BODY	GUL D&304;REK	Received

177-P1	Genetic investigation of children with syndromic prenatal onset short stature	THAIS HOMMA	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

178-P3	Congenital Hyperinsulinism in Children with Beckwith-Wiedemann syndrome	Diliara Gubaeva	Received

178-P2	Oxidative homeostasis dysregulation may promote pathogenesis of cardio-metabolic complications in childhood obesity	Domenico Corica	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

179-P3	Comparison of the phenylketonuria phenotypes in Qazvin province before and after neonatal screening until 2017	Fatemeh Saffari	Received

179-P1	Beckwith Wiedemann syndrome: first international consensus regarding diagnosis and clinical management.	FREDERIC BRIOUDE	Received

179-P2	Body composition parameters, systemic inflammation and metabolic syndrome manifestations in children and adolescents	Eirini Christaki	Received

180-P1	Silver Russell and Beckwith-Wiedemann syndromes: Mosaic distribution of epigenetic anomalies	PHAM Aurélie	Received

180-P2	Relationships between Obesity Parameters and Urinary Concentrations of Phthalates and Phenols in Korean Girls	Mi-Jung Park	Received

180-P3	From Hypoglycemia to Hyperglycemia	Ho-chung YAU	Received

181-P3	Population screening of hypophosphatasia. A metabolopathy to consider.National multicentric study	Ignacio Diez	Received

181-P2	Clinical characteristics of congenital hyperinsulinism caused by dominant KCNJ11/ABCC8 mutations.	Maria Melikyan	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

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

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

182-P3	Dumping Syndrome in a neonate with Esophageal Atresia Surgery	Jennyfer Monroy Espejo	Received

183-P2	CONGENITAL HYPERINSULINISM: MANAGEMENT & OUTCOME IN WEST OF SCOTLAND	Khadiga Eltonbary	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

183-P3	Diagnosis and treatment of persistent hyperkalemia in newborn twins ----Rare case report of Gordon syndrome	jun zhang	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

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

184-P2	20 cases of congenital hyperinsulinism in Ukraine	Evgenia Globa	Received

185-P3	HYPERINSULINEMIC HYPOGLYCAEMIA SYNDROME IN SMALL-FOR-GESTATIONAL AGE NEWBORNS: CLINICAL CHARACTERISTICS AND GENETIC STUDY	Pamela Yesquen Salcedo	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

186-P2	Potentially modifiable predictors of adverse neonatal outcomes in women with gestational diabetes mellitus (GDM).	Maria-Christina Antoniou	Received

186-P1	Maternal uniparental disomy for chromosome 20: physical and endocrinological characteristics of six patients	Sayaka Kawashima	Received

186-P3	Pediatric insulinoma: A case report	Pathikan Dissaneevate	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

187-P2	A boy with diazoxide unresponsive congenital hyperinsulinism due to a homozygous ABCC8 missense mutation previously reported to be dominant	Sonya Galcheva	Received

188-P2	Diazoxide unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation.	YASMINE OUAREZKI	Received

188-P1	Mutations in SHOX, GHR and IGFALS genes among Indian children with idiopathic short stature	Vandana Jain	Received

188-P3	Weight outcome ininfants with prolonged hyperinsulinemic hypoglycemia treated with Diazoxide versus those with spontaneous resolution	SURESH CHANDRAN	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

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

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

190-P1	Overview of leading causes of death among French patients with Prader-Willi Syndrome, 2004-2014	Dibia Liz Pacoricona Alfaro	Received

190-P2	Hepatoblastoma and Wilms Tumour in an infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism	SAURABH UPPAL	Received

191-P3	Transient Central Hypothyroidism due to Maternal Graves disease	YUKIE IZUMITA	Received

191-P2	Association between Rubenstein-Taybi Syndrome and hyperinsulinaemic hypoglycaemia	Ranna El-Khairi	Received

192-P3	Good Growth Response to Growth Hormone Therapy in Short Children with Normal Growth Hormone Secretion	AHMED EL AWWA	Received

192-P2	Hyperinsulinemic hypoglycemia in congenital disorder of glycosylation type-1a (CDG-1a)	Dogus Vuralli	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

193-P2	A rare cause of hyperinsulinemic hypoglycemia: Costello syndrome	Dogus Vuralli	Received

193-P1	McCune-Albright-Syndrome: clinical and genetic study in a large cohort of pediatric patients.	Nadezhda Makazan	Received

194-P3	Growth hormone treatment: does timing matter?	Bernardo Marques	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

195-P2	THE BENEFIT OF UNIVERSAL NEONATAL SCREENING FOR HYPOGLYCEMIA	Georges Nicolas	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

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

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

196-P2	Prematurity of 23 or less weeks gestation is a risk for transient late-onset hyperglycemia in neonates	Takeru Yamauchi	Received

196-P3	Main discrepancies between predicted and observed growth responses with iGRO in children treated with GHr in Spain	Cristina Mora Palma	Received

197-P1	A single centre experience of managing a series of childhood macro/giant-prolactinoma	Antonia Dastamani	Received

197-P2	An unusual cause of neonatal hyperglycemia case report	Joana Matos	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

198-P3	Growth hormone deficiency in neurofibromatosis: report of four cases	Elisa Guidoni	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

198-P2	NEONATAL HYPOCALCEMIA DUE TO MATERNAL HYPOVITAMINOSIS D: A COHORT OF CHILDREN IN A REGION OF NORTHERN SPAIN	maria laura Bertholt	Received

199-P2	Evaluation of vitamin D status and its correlation with gonadal function in children at mini-puberty	Suna KILIN	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

200-P3	Small for gestational age patients with premature treatment discontinuation: their journey in French, real-life settings	Jean-Pierre Salles	Received

200-P2	Systemic pseudohypoaldosteronism type 1 due to 3 novel mutations in SCNN1A and SCNN1B genes; report of 3 cases	Atilla Cayir	Received

200-P1	PROKR2 Mutations in Patients with Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency	Asl&305; Derya Kardelen	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

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

201-P2	Postnatal Growth of Infants with Neonatal Diabetes: Insulin pump (CSII) versus Multiple Daily Injection (MDI) therapy	ashraf soliman	Received

202-P2	Serum vaspin concentration in full-term, appropriate-for-gestational-age newborns: effect of early-onset infections	Ma&322;gorzata Stojewska	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

202-P3	Final adult height after growth hormone treatment in patients with Turner syndrome	Jungmin Ahn	Received

203-P1	Serum concentrations of the endocrine disruptors-organochlorine pesticides (OCPs) in Greek children with Neurodevelopmental Disorders	Gerasimos Makris	Received

203-P3	Results of mecasermin treatment in pediatric patients evaluated for severe and partial primary deficiency of IGF-1	Karolina Stozek	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

204-P2	Assessment of the stretched penile length in Sri Lankan newborns	Dona Udeni Anuruddhika Kollurage	Received

204-P3	Children born small for gestational age treated with growth hormone: evolutionary aspects.	Verónica María Padín Vázquez	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

205-P1	A paternally inherited familial precocious puberty caused by a novel MKRN3 frameshift variant	Jessica Odone	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

206-P1	MKRN3 levels in girls with central precocious puberty during GnRHa treatment: a longitudinal study	anna grandone	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

206-P2	Identification of three novel GLI2 gene variants associated with Hypopituitarism	Lidia Castro-Feijoo	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

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

208-P3	Cost-effectiveness of growth hormone therapy in children in Russia	Maria Vorontsova	Received

208-P1	Testicular Development And Puberty In Boys With Duchenne Muscular Dystrophy: Results From The ScOT-DMD Study	Melissa Denker	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

209-P1	Exposure to BPA and phthalates and timing of puberty in girls	annalisa deodati	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

209-P3	Vitamin D status in children with isolated idiopathic Growth hormone deficiency (GHD) in North and Central Greece	Maria Xatzipsalti	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

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

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

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

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

211-P2	Growth hormone treatment for short stature associated with TRNT1 deficiency: a case series	Yuezhen Lin	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

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

212-P2	Novel case of short stature and co-occurrence of SHOX gene mutation and Fanconi Anemia	Aristotle Panayiotopoulos	Received

213-P2	Different genetic causes of short stature in a family	Alev Tulun	Received

213-P3	Role of Insulin like growth factors on the growth parameters in children with acquired hypothyroidism: An analysis.	Ruchi Goel	Received

213-P1	Insights in promoter transactivation activity of CBX2.	Dirk Hart	Received

214-P3	Two Siblings With Short Stature	V. SRI NAGESH	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

214-P2	Incidence of Cranial MRI abnormalities in Patients with Isolated Growth Hormone Deficiency: 20 Years of Results	Nadia Amin	Received

215-P2	SYSTEMATIC PROSPECTIVE STUDY OF EYE FUNDUSCOPY BEFORE AND AFTER STARTING TREATMENT WITH GROWTH HORMONE IN 289 PATIENTS.	Eduard Mogas Viñals	Received

215-P3	RHGH replacement therapy and side- effects: ? retrospective study of 10 years	STAVROULA PARASTATIDOU	Received

215-P1	Mutations involving nuclear receptors and their cofactors as a major cause of 46,XX DSD	Ken McElreavey	Received

216-P1	SDgeneMatch, a new tool to aid the identification of the genetic causes of DSD	Ken McElreavey	Received

216-P2	Incidence and prevalence of growth hormone deficiency in the Russian Federation an analysis of two registries	Maria Vorontsova	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

217-P2	The BSPED National Growth Hormone (GH) Audit: Trends in prescribing from 2013-2016	Leena Patel	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

218-P2	The Rationale and Design of TransCon GH	Eva Mortensen	Received

218-P1	Primary gonadal dysgenesis in male 46,XY patients with NR5A1 variants predominantly affects Sertoli cell function	Julia Hoppmann	Received

219-P1	Evaluation of Genetic Etiology in Patients with 46,XY Disorders of Sex Development:One Center Experience	SUKRAN POYRAZOGLU	Received

219-P2	Baseline Demographics of the TransCon Growth Hormone Phase 3 heiGHt Trial	Eva Mortensen	Received

219-P3	IS GROWTH HORMONE DEFICIENCY A CONTRIBUTOR TO SHORT STATURE IN CUTIS LAXA SYNDROME?	Alice Albu	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

220-P3	EFFECT OF SICKLE CELL DISEASE ON GROWTH AND PUBERTY	Anjumanara Omar	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

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

221-P3	Two Siblings with Alstrm Syndrome	Ayse Nurcan Cebeci	Received

221-P2	GROWTH HORMONE TREATMENT IN CHILDREN BORN SMALL FOR GESTATIONAL AGE (SGA)	Aleksandra Janchevska	Received

222-P2	Height perception of children with Growth Hormone Deficiency: influencing factors and links to psychosocial functioning	Chrysoula Drosatou	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

222-P3	Development of an Online Learn-pro Module to support Health Care Professionals knowledge about Growth and Puberty	barbara Wardhaugh	Received

223-P2	Health lifestyle and obesity of adult patients with Congenital Isolated Growth Hormone Deficiency treated in childhood	Zvi Laron	Received

223-P3	COELIAC DISEASE IN TURNER SYNDROME MORE FREQUENT THAN EXPECTED.	BAZ OUIDAD	Received

223-P1	Sex-Differences in Reproductive Hormones during Mini-Puberty in Infants with Normal and Disordered Sex Development	Marie Lindhardt Ljubucuc	Received

224-P2	Factors influencing Health Related Quality of Life in children/adolescents with Growth Hormone Deficiency	Chrysoula Drosatou	Received

224-P3	A 14-year-old boy with Simpson- Golabi- Behmel syndrome- case report	Beata Sawicka	Received

224-P1	TheExternalGenitaliaScoreto describe external genitalia in male and female infants. A Europeanmulticenter validation study	Saskia van der Straaten	Received

225-P3	Central precocious puberty in a girl with Silver Russell syndrome	Beata Wikiera	Received

225-P2	HEALTH-RELATED QUALITY OF LIFE AND PSYCHOSOCIAL FUNCTIONING IN YOUNG ADULTS BORN SGA AFTER GH/GNRHA TREATMENT	Wesley Goedegebuure	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

226-P1	You can put ideas into their heads: Parental concerns about childrens participation in DSD research.	Maia Thornton	Received

226-P3	Etiologies of Short Stature in Pedaitric Endocrine Clinic in Northwest Region (Trakya) of Turkey	Emine Dilek	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

227-P3	Auditing presentation, investigations and management of Turners syndrome	Buddhi Gunasekara	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

227-P1	Testosterone levels in newborn boys and girls related to penile length, Anogenital distance (AGD) and External Genitalia Score (EGS)	Jon Sigurdsson	Received

228-P2	Reliability of Clonidine Testing for the Diagnosis of Growth Hormone Deficiency in Children and Adolescents	Anastasia Ibba	Received

228-P1	Clinical Factors That Determine Surgical Outcome Following Hypospadias Repair	Fahad Aljuraibah	Received

228-P3	CHILDREN BORN SMALL FOR GESTATIONAL AGE: CATCH-UP GROWTH DURING THE FIRST FOUR YEARS OF LIFE	concepcion martin	Received

229-P2	Area Under the Curve of Growth Hormone, an additional tool in assessing stimulation test results.	Yonatan Yeshayahu	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

229-P1	Prevalence of hypogonadism in prepubertal boys with cryptrochdism.	Romina Grinspon	Received

230-P3	ENDOCRINOLOGICAL EVALUATION OF GIRLS WITH TURNER SYNDROME ATTENDING ALEXANDRIA UNIVERSITY CHILDRENS HOSPITAL	Doaa Khater	Received

230-P1	Testicular ultrasound to stratify gonadal hormone references in a Norwegian study of male puberty	Andre Madsen	Received

230-P2	Evaluation of Spontaneous Nocturnal GH Secretion: One versus two consecutive Nights	Gunter Simic-Schleicher	Received

231-P3	A long follow-up in a young patient with Atypical Progeroid Syndrome	scarano emanuela	Received

231-P1	Altered vascular function in boys with hypospadias- role of reactive oxygen species	Angela Lucas-Herald	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

232-P1	Gonadectomy for Adults With DSD Conditions In The International Disorders of Sex Development Registry	Angela Lucas-Herald	Received

232-P2	The predictive role of IGF-1 on irradiation-dependent growth hormone deficiency (GHD) in childhood cancer survivors (CCS)	Alessandro Cattoni	Received

232-P3	GH treatment in Kabuki syndrome: a case report	Elisa Guidoni	Received

233-P3	GH treatment in oto-spondylo-megaepiphyseal dysplasia: a case report	Elisa Guidoni	Received

233-P1	Phenotypic And Genetic Assessment Of Boys With A Suspected XY Disorder Of Sex Development	Malika Alimussina	Received

234-P1	Pediatricians Attitudes and Beliefs towards Transgender Persons	Nitsan Landau	Received

234-P3	Hepatic glycogen synthasedeficiency associated with growth hormone deficiency: A case report	Hakan Dneray	Received

234-P2	HIGH PROTEIN NUTRITIONAL SUPPLEMENTATION INCREASES SERUM IGF-I CONCENTRATIONS IN SHORT CHILDREN WITH LOW IGF-I	Elin Mattsson	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

235-P3	Analysis of genetic mutations in a Chinese patient affected with Noonan Syndrome	HUI HUANG	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

236-P2	Artificial neural networks for prediction final height in children with growth hormone deficiency.	Anna Gavrilova	Received

236-P3	A novel homozygous mutation in ERCC8 cause Cockayne Syndrome a in a Chinese family	HUI HUANG	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

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

238-P2	TITLE-Growth Hormone therapy and its challenges in GH Deficient cases in a multinational population-a sneak-peek	DEEPTI CHATURVEDI	Received

238-P3	Title: Hypothyroidism and Growth Hormone (GH) Deficiency, A Spotlight on De Novo Chromosomal 20p11.2 Deletion	Idris Mohammed	Received

238-P1	Effect of intrauterine growth restriction on ovarian follicle pool in rats	Valentina Pampanini	Received

239-P2	HEART AND AORTA ANOMALIES IN TURNER SYNDROME AND RELATION WITH KARYOTYPE	Asl&305; Derya Kardelen	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

239-P3	PHARMACOECONOMIC AND ADHERENCE ANALYSIS in GROWTH HORMONE ACCORDING TO GALENIC PRESENTATION In vivo study vs in vitro	Ignacio Diez	Received

240-P3	The expression of cytokines in SGA children throughout lactation allows to characterize early the type of cath-up	Ignacio Diez	Received

240-P2	The validation of an automated bone age assessment in girls with Turner syndrome a pilot study	Ondrej Soucek	Received

240-P1	Anti-Mullerian Hormone (AMH) concentrations and reduced Appendix Testis Estrogen Receptor expression in Cryptorchidism	Eirini Kostopoulou	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

241-P3	SMALL STATURE: A singular difference for accessing to job	Ignacio Diez	Received

241-P2	Turner Syndrome and Autoimmune Thyroid Disease: pecularities of evolution in 93 Turner Syndrome patients.	CRISTINA DUMITRESCU	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

242-P2	Unusual clinical manifestations in Turner syndrome	Natallia Akulevich	Received

242-P1	AMH LEVEL OF INFANTS WITH PREMATURE THELARCHE AND POSSIBLE RELATIONSHIP BETWEEN AMH AND MINI-PUBERTY	nursel muratoglu sahin	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

243-P3	Increased serum activity of liver aminotransferases in young patients with Turner Syndrome	Ma&322;gorzata Wójcik	Received

243-P1	Circulating makorin ring finger protein 3 levels predict central precocious puberty in girls	Hwal Rim Jeong	Received

244-P2	Familial Turner Syndrome: Case Report	Jimena Lopez Dacal	Received

244-P1	Polycystic Ovarian Syndrome in Adolescents: Characterising the Clinical Phenotype and the Role of Precision Medicine	Harriet Gunn	Received

245-P2	Clinical review of 7 patients affected with 49,XXXXY syndrome	Jacobo Pérez Sánchez	Received

245-P1	Thyroid function in central precocious puberty girls	Hyo-Kyoung Nam	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

246-P2	Poor weight gain in Prader-Willi Syndrome not always over-restriction consider Coeliac Disease	Mina Lateva	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

247-P2	Growth Hormone Unmasked Laryngomalacia and Worsened Obstructive Sleep Apnea in Infants with Prader-Willi Syndrome	Parisa Salehi	Received

247-P3	A Rare Chromosomal Disorder, Trisomy 4p	MERVE NUR HEPOKUR	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

248-P3	Prediction of response to growth hormone treatment in Korean girls with Turner syndrome	Mo Kyung Jung	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

249-P2	GrowInform a campaign for early diagnosis and treatment of growth disorders	Rosica Stoycheva	Received

250-P2	Growth and body composition of term healthy Indian infants from birth to 2 years of age	Vandana Jain	Received

250-P3	Prader-Willi Patient with Rectal Bleeding Experience in Center for Rare Endocrine Disordesrs in Varna, Bulagria.	Nikolinka Yordanova	Received

250-P1	Thyroid scintigraphy in the diagnosis of Congenital Hypothyroidism	Chris Worth	Received

251-P3	MOSAICISM 47XXX/45X0, A CASE REPORT	Renata Pinto	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

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

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

252-P2	Final Results of NordiNet International Outcome Study: Key Outcomes in Paediatric Patients	Michel Polak	Received

252-P1	Morning versus Bedtime Levothyroxine Administration: What is the Choice of Children?	ONUR AKIN	Received

253-P2	INFLUENCE OF PUBERTY ON ADULT HEIGHT OF SGA CHILDREN TREATED WITH GH	Juan Pedro Lopez Siguero	Received

253-P3	Tall Stature: A Diagnosis Is Somtimes Difficult	kherra sakina	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

254-P3	Title: Woodhouse-Sakati Syndrome: Clinical and Molecular Study on a Qatari Family with C2orf37Gene MutationMCEPASTEBIN	Katarina Gluic	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

254-P1	Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH beta subunit Gene	TARIK KIRKGOZ	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

255-P3	Factors affecting height velocity in normal prepubertal children	Seul Ki Kim	Received

255-P2	Clinical and cost-effectiveness of GH treatment for children in Wales	Raluca-Monica Pop	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

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

257-P1	Results of the hTPO mutational screening in Bulgarian patients with congenital hypothyroidism (CH)	Iva Stoeva	Received

258-P3	LATE REFERRAL OF SIBILINGS WITH COMBINED PITUITARY HORMONE DEFICIENCY (PROP1)	Snijezana Hasanbegovic	Received

258-P2	Clinical and Molecular Analyses of 24 Patients with Beckwith-Wiedemann Syndrome	WEI LU	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

259-P2	Unusual case of combination of Beckwith-Wiedemann Syndrome and SHOX gene deficiency	Marco Pitea	Received

259-P1	A novel mutation of IGSF1 gene	ELLADA SOTIRIDOU	Received

260-P3	PRADER WILLI SYNDROME: CLINICAL PROFILE	Vasundhara Chugh	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

260-P1	Multinodular goiter in childhood: a diagnostic gateway for screening DICER1 syndrome	isabelle OLIVER PETIT	Received

261-P1	A novel DICER1 mutation identified in a family with the multinodular goiter of children	Keisuke Nagasaki	Received

261-P2	Two different variants of short stature homeobox-containing gene (SHOX) mutation in the same family	Stefanie Graf	Received

261-P3	Leri-Weill Syndrome phenotype with atypical cytogenetic finding	Vilhelm Mladenov	Received

262-P2	Identification of a novel heterozygous ACAN mutation in a patient with non-syndromic short stature	Partenop Cristina	Received

262-P3	Deletion of 12q12 increases the risk of growth retardation and intellectual disability	Ying Weng	Received

263-P2	Genetic investigation of Short Stature: a case report of Complex Constitutive rearrangement involving chromosome 15	Renata Pinto	Received

263-P1	Expression of ZnT8 transporter in thyroid tissues from patients with immune and non-immune thyroid diseases	Artur Bossowski	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

265-P3	Insulinoma as initial presentation of Multiple Endocrine Neoplasia type 1	Ada Borowiec	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

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

266-P1	Childhood thyroid autoimmunity and relation to islet autoantibodies in children at risk for type 1 diabetes	Berglind Jonsdottir	Received

266-P2	A novel FGFR1 mutation in Kallmann syndrome with growth hormone deficiency	Maria Chiara Pellegrin	Received

266-P3	Assessment of ovarian reserve in young women with Hashimoto thyroiditis - a pilot study	Anna Wedrychowicz	Received

267-P3	Unusual clinical presentation of autoimmune polyendocrinopathy type 1.	Federico Baronio	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

268-P2	A new mutation in IHH gene causing severe short stature.	adalgisa festa	Received

268-P1	Analysis of zinc- transporter ZnT8 autoantibodies in children and adolescents with autoimmune thyroid diseases	Justyna Michalak	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

269-P2	CASE REPORT: ELLIS VAN CREVELD SYNDROME WITH A NOVEL MUTATION	elif sb	Received

269-P3	GRAVES DISEASE IN CHILDREN WITH T1DM: A REPORT OF THREE CASES	Ngoc Can Thi Bich	Received

269-P1	The association between TSHR, IFIH1 and ETV5 polymorphisms with Graves disease and diabetes mellitus type 1 in children	Karolina Stozek	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

270-P3	Case report: Neonatal McCune-Albright syndrome with juvenile ovarian granulosa cell tumor in a 4 months old girl	Esther Schulz	Received

271-P2	Unexpected growth patterns in Branchio-Oto-Renal syndrome.	Emma Clarke	Received

271-P3	Polyostotic Fibrous Dysplasia of McCune Albright Syndrome responding to intravenous Zoledronate therapy	Ganesh HK	Received

272-P3	Two Cases of Costello Syndromeand Literatures Review	Zhuan-nan Jiang	Received

272-P2	Mild autistic spectrum disorder in a 33 year-old male Japanese patient with Temple syndrome	Shuichi Yatsuga	Received

273-P3	ENDOCRINE COMPLICATIONS IN BETA-THALASSAEMIA MAJOR CHILDREN	Mirela Iancu	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

274-P2	KBG syndrome: our experience and unreported clinical features.	emanuela scarano	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

275-P3	Unusual case of Autoimmune Polyglandular Syndrome.	Nino Abdushelishvili	Received

275-P2	Growth of Infants Born by Intracytoplasmic sperm injection (ICSI) Technique	Ashraf Soliman	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

276-P3	AUTOIMMUNEPOLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY: A CASE REPORT	Ozlem Nalbantoglu	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

277-P3	WOLMAN DISEASE: LONG-TERM ENDOCRINE AND METABOLIC COMORBIDITIES	Rachel Bello	Received

278-P2	Effects of inhaled corticosteroids and montelukast on growth and body mass index in children with asthma	onur AKIN	Received

279-P3	NEAR ELECTROMAGNETIC FIELDS - INDUCED SYNDROME: UNSUSPECTED AND NEWLY RECOGNISED	STYLIANI GERONIKOLOU	Received

280-P3	POLYCYSTIC OVARY SYNDROME GENE/GENE PRODUCTS INTERACTION NETWORK	STYLIANI GERONIKOLOU	Received

280-P2	Skeletal Disproportion And Growth Impairment In Glucocorticoid Treated Boys With Duchenne Muscular Dystrophy	Kao Kung-Ting	Received

281-P3	BASAL METABOLIC RATE AS MODERATOR OF INFLAMMATION IN PCOS	STYLIANI GERONIKOLOU	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

282-P3	Insight of differential diagnosis of DAX-1 from two patients with elevated testosterone in early infancy	Tang Li	Received

282-P2	VESICO-URETERAL REFLUX AND EFFECT ON GROWTH INDICES.	Georges Nicolas	Received

283-P3	Rapid onset and progression of chronic kidney disease in a child with Autoimmune Polyglandular Syndrome Type 1.	Vasiliki Rengina Tsinopoulou	Received

284-P3	Infant with osteogenesis imperfecta and panhypopituitarism: a case report	Noor Arliena Mat Amin	Received

284-P2	ENDOCRINE AND METABOLIC COMPLICATIONS IN CHILDREN AND ADOLESCENTS WITH SICKLE CELL DISEASE: AN ITALIAN COHORT STUDY	Lorenzo Iughetti	Received

285-P2	Bone marrow failure in Mc Cune Albright Syndrome	Katja Wechsung	Received

285-P3	PANHYPOPITUITARISM WITH TALL STATURE DIAGNOSED IN A 20 YEARS OLD BOY	Andrea Forrester	Received

286-P3	Post-traumatic hypopituitarism caused by pituitary stalk transection	Anna Ruszala	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

287-P3	Invasive macroprolactinoma with cabergoline induced cerebrospinal fluid rhinorrhoea in childhood	Antonia Dastamani	Received

287-P2	Endocrine challenges in patients with thalassemia	Tanja Christa Haamberg	Received

288-P3	Bilateral optic nerve hypoplasia revealing septo optic dysplasia or De Morsier syndrome: A case report.	ARIBI YAMINA	Received

288-P2	Can oral iron chelation therapies reduce endocrine complications in -thalassemia major patients?	PARASTOO ROSTAMI	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

290-P2	Successful treatment of severe atopic dermatitis with calcitriol and paricalcitol in an 8-year old girl.	Christina Bothou	Received

290-P3	An Interesting Etiology in Childhood Central Diabetes Insipidus HIBERNOMA	Aya Trel Ergr	Received

291-P3	Neonatal panhypopituitarism with hypoglycemia, edema, inspiratory stridor and cholestasis	Benita Momm	Received

291-P2	Hypoglycemia in adolescence as the presenting sign of familial MEN1	Justine BAILLEUL	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

292-P2	ALDOSTERONE, RENIN, SODIUM AND POTASSIUM EXCRETION IN NORMOTENSIVE PREPUBERTAL CHILDREN	Alejandro Martinez-Aguayo	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

294-P3	Growth hormone deficit associated to complex arteriovenous malformation case report	Mirela Mogoi	Received

296-P3	Analysis of Influencing Factors on Bone Maturation in Girls with Central Precocious Puberty(CPP)	Gi-min Lee	Received

296-P2	Military conflict at the east of ukraine and physical development of children and adolescents	Svetlana Turchina	Received

297-P3	Is Prematre Adrenarch Associated With Precocious Puberty Via Kisspeptin?	GUL D&304;REK	Received

297-P2	POLYCYSTIC OVARY SYNDROME METABOLIC SYNDROME PREDISPOSITION IN PUBERTY	STYLIANI GERONIKOLOU	Received

298-P2	Fanconi-Bickel Syndrome in Sudanese children, Case series	Salwa Elhassan	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

299-P3	A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding	Harjoedi Harjoedi	Received

300-P3	Evaluation of Cases with Pubertal Gynecomastia	Havva Nur Kendirci	Received

300-P2	Somatostatin Experiment in Prohormone Convertase Deficiency	emine demet akba&351;	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

301-P2	Efficacy and safety of triptorelin 3-monthformulationin patients with centralprecocious puberty and BMI evaluation.	Rossella Gaudino	Received

302-P3	EFFECT OF TRIPTORELINE IN PATIENTS WITH CENTRAL PRECOCIOUS PUBERTY AT CHILDRENS HOSPITAL 1.HCMC.VIET NAM	Huyen Tran	Received

302-P2	Triptorelin Test in Diagnosing Central Precocious Puberty	Rade Vukovic	Received

303-P2	Foot length growth is a novel marker of early puberty	Ben Balzer	Received

303-P3	Morning unstimulated hormone, a good screening tool for diagnosing central precocious puberty.	Dong Min Lee	Received

304-P2	Ultrasound-based measurements of testicular volumeObserver agreement and comparison with Prader orchidometry	Ninnie Oehme	Received

307-P3	Premature adrenarche and pseudohypoparathyroidism mechanistically linked or coincidence?	Jessica Odone	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

308-P2	A NOVEL INACTIVATING COMPOUND HETEROZYGOUS MUTATION IN KISS1R/GPR54: CASES OF THREE SIBLINGS	Ozlem Nalbantoglu	Received

309-P3	GLP-1 receptor agonist in a patient with craniopharyngioma-related obesity.	Maria-Christina Antoniou	Received

309-P2	MKRN3 gene mutations in a cohort of patients with central precocious puberty	Magdalena Avbelj Stefanija	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

311-P2	Incidence of delayed puberty. A population-based study in a county in central Sweden.	Maria Rodanaki	Received

311-P3	Congenital hypopituitarism associated with complex cranio-vertebral junction anomalies	Mariella Valenzise	Received

312-P2	Observer agreement in ultrasound assessment of pubertal breast development	Ingvild Srvold Bruserud	Received

312-P3	Premature thelarche followed by acute lymphoblastic leukemia in a 1,5 year old girl	Ana Stamatova	Received

313-P3	Two cases of non-syndromic congenital unilateral hypoplasia in one family	Ana Stamatova	Received

313-P2	Neuroendocrine consequences of Hypothalamic Hamartoma and their Imaging (MRI) and Surgery Correlates.	Beatriz Corredor Andrés	Received

314-P2	THE START PREDICTORS OF PUBERTY IN BOYS WITH CONSTITUTIONAL DELAY OF PUBERTY	Oleg Latyshev	Received

314-P3	Klinefelter Syndrome with Ambiguous Genitalia in a Child	nur rochmah	Received

315-P3	The change in growths velocity in patients with premature puberty receiving treatment with analogues of lyuliberin	Olga Berseneva	Received

316-P2	Gonadotropin Levels And Frequency Of Testosterone Supplementation In Adolescents With Klinefelter Syndrome	XANTHIPPI TSERETOPOULOU	Received

316-P3	THE EFFICACY OF TREATMENT IN VIETNAMESE CHILDREN WITH CENTRAL PRECOCIOUS PUBERTY	Quynh Huynh Thi Vu	Received

317-P3	THE CHARACTERISTICS OF CENTRAL PRECOCIOUS PUBERTY AT CHILDRENS HOSPITAL 2 IN VIETNAM	Quynh Huynh Thi Vu	Received

318-P2	SOX3 gene duplication associated with midline CNS malformations, hypopituitarism and neurodevelopmental abnormalities: 5 unrelated cases	Garima Chawla	Received

318-P3	SIG (Special Interest Group)-ENDOPED/RUTE (Brazil): Seven years integrating pediatric endocrinology centers throughout the country	Ricardo Arrais	Received

319-P2	AN 18 MONTH OLD BOY WITH HYPOGLYCEMIC CONVULSION AND OBESITY DUE TO POMC DEFICIENCY	Sare Betul Kaygusuz	Received

319-P3	The relationship between prolactin and development of puberty in girls with early breast development	Seong Yong Lee	Received

320-P3	Central Precocious Puberty appeared in infancy period in a patient of Sotos Syndrome	tu&287;ba etin	Received

320-P2	Pituitary stalk interruption syndrome (PSIS) is not a rare cause of the congenital hypopituitarism	Erdal Eren	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

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

322-P2	PRIMARY EMPTY SELLA SYNDROME AND CLNICAL ENDOCRINE POLYMORPHISMS IN CHILDREN. A REPORT OF 15 CASES.	SIMON KAYEMBA-KAYS	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

323-P2	Growth hormone deficiency (GHD) in a patient with persistence of the craniopharyngeal canal with cephalocele	Silvana Caiulo	Received

324-P2	Endocrine-metabolic characterization of pediatric patients with craniopharyngioma. A single-centre cohort study.	Stefania Pedicelli	Received

324-P3	Challenges in managing 46, XY Partial gonadal dysgenesis in Saudi Arabia	AMIR BABIKER	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

325-P3	A paternally inherited NR5A1 mutation in a case of 46,XY partial gonadal dysgenesis	Andréa Maciel-Guerra	Received

326-P3	CLINICAL PRESENTATION AND CHARACTERISTICS OF DSD IN KENYAN CHILDREN AND ADOLESCENTS	Anjumanara Omar	Received

326-P2	Pituitary adenomas in children and adolescents: a retrospective single-centre analysis	Thomas Breil	Received

327-P3	Evolutive profile of pauci-symptomatic forms of Mc Cune Albright syndrome	audrey cartault	Received

327-P2	Changes in body composition in male adolescents with GH deficiency are diagnostic during transition	Gerhard Binder	Received

328-P3	A 45X0/46XY Girl Diagnosed with Prepubertal FSH Elevation	Belma Haliloglu	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

329-P2	Gender-related differences in etiological distribution of organic causes of central precocious puberty	Dogus Vuralli	Received

329-P3	About a case of Leydig cell tumor associated with central precocious puberty	bensalah Meryem	Received

330-P2	Final adult height in girls with idiopathic central precocious puberty treated with monthly leuprorelin acetate VS triptorelin acetate	Voraluck Phatarakijnirund	Received

330-P3	Gender dysphoria	Birgit Lidwall	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

331-P3	GnRH Analogues and Cross-Sex Hormonal therapy: side effects in Transgender Youth	Cristina Mora Palma	Received

332-P3	Klinefelter syndrome with low gonadotropin levels	Daria Berdyugina	Received

332-P2	Basal Serum LH Level as a Diagnostic Test for Girls with Early Phase of Central Precocious Puberty	Somboon Wankanit	Received

333-P2	Determination of urinary metabolic profiles of children with central and peripheral precocious puberty	derya bulu&351;	Received

333-P3	YOUNG MALE ADOLESCENT WITH GENDER DYSPHORIA (GD)/GENDER INCONGRUENCE- A CASE PRESENTATION	Eirini Dikaiakou	Received

334-P3	Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty and early puberty	Eun Young Kim	Received

334-P2	Hypertension during GNRH analogues therapy in a 10-year-old girl	massimo barreca	Received

335-P2	The Effect Of Polychlorinobiphenyls On Premature Puberty In Girls	Samim zen	Received

335-P3	DSD in Ukraine: our experience	Evgenia Globa	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

336-P3	A Turkish family with 46,XY disorder of sex development due to 17b-hydroxysteroid dehydrogenase type 3 deficiency	fatih grbz	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

337-P3	Normal External Genitalia in a Female with Classic, Salt-Wasting 21-hydroxylase deficiency	Hadeel Alsarraj	Received

338-P2	Physical assessment in Chinese children with 5a-reductase type 2 de?ciency	Xiu Zhao	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

339-P3	Analysis of genetic mutations in a Chinese pedigree affected with idiopathic hypogonadotropic hypogonadism Syndrome	HUI HUANG	Received

339-P2	Results of exome sequencing in disorders of sex development	Marlies Kempers	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

341-P2	Evaluation of Three Patients with 46,XY Gonadal Dysgenesis Due to Desert Hedgehog Gene Mutations	SUKRAN POYRAZOGLU	Received

341-P3	Cytogenetic spectrum of Ovotesticular Disorder of Sex Development in Egyptian DSD patients	inas mazen	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

343-P2	Clinical, biochemical, structural and functional characterization of a novel P450 oxidoreductase mutation causing virilization in a 46,XX patient	Núria Camats	Received

343-P3	Genital abnormalities and management outcomes as seen in the University of Port Harcourt Teaching Hospital	Iroro Yarhere	Received

344-P3	A case report: A girl with 46,XY karyotype and disorder of androgen synthesis	Jasna uput Omladi&269;	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

345-P3	THE POSITIVE EFFECT OF THE LOW-DOSE CONTRACEPTIVE ON THE COURSE OF CYSTIC FIBROSIS IN THE ADOLESCENT FEMALE	Juliana Ferenczova	Received

345-P2	Histopathologic characterization of patients with 46,XX testicular and ovotesticular disorders of sex development.	Esperanza Berensztein	Received

346-P2	Current medical care of children and adolescents with disorders/differences of sex development in Switzerland	Grit Sommer	Received

346-P3	Ovotesticular Disorder of Sexual Development: 31 cases followed-up in a single-center in Brazil	Leandra Steinmetz	Received

347-P2	Clinical, Laboratory and Molecular Genetic Findings of Patients with 17-Hydroxysteroid Dehydrogenase3 Deficiency	SUKRAN POYRAZOGLU	Received

347-P3	Genital swelling and ovarian stimulation syndrome in an extremely preterm infant	Maria Cristina Azcona	Received

348-P3	Significant penile growth with local DHT-gel in an infant with 17beta-HSD-deficiency	Maria Halldin Stenlid	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

349-P2	A 46,XX female with WT1 mutation, congenital nephrotic syndrome and a complex disorder of sex development	Sara Ciccone	Received

349-P3	Mother and baby diagnosed Noonan syndrome with dysmorphic findings	Mehmet Keskin	Received

350-P2	Psychological gender features and social abilities and in adolescent girls influence of obesity and hyperandrogenism	Agnieszka Zachurzok	Received

351-P3	A Case Report of Spironolactone Treatment for Beckers Nevus Associated Ipsilateral Breast Hypoplasia	Abhilasha Banerjee	Received

351-P2	Two unrelated cases of severe insulin resistance due to insulin receptor mutation discovered during adolescence	azgal maryam	Received

352-P2	A Systematic Review Of Reported Outcomes For Hypospadias	Tina Lund Leunbach	Received

352-P3	NEW MUTATIO IN 5 ALFA REDOCTASE: A five-month-old infant with a karyotype of 46 xy	setila dalili	Received

353-P2	Young transgender peoples attitudes to fertility preservation and practice	elena Monti	Received

353-P3	A NOVEL COMPOUND HETEROZYGOUS MUTATION IN CYP19A1 RESULTING IN AROMATASE DEFICIENCY WITH NORMAL GONADOTROPIN LEVELS AND OVARIAN TISSUE	Sezer Acar	Received

354-P2	ETIOLOGY OF DISORDERS OF SEX DEVELOPMENT IN KENYAN CHILDREN AND ADOLESCENTS	Anjumanara Omar	Received

354-P3	Emblematic case CAH	Silvia Chahin	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

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

356-P3	Paediatric doctors experience and knowledge of the initial management of neonatal ambiguous genitalia	Sinead McGlacken-Byrne	Received

356-P2	Diagnostic experiences and concerns in adolescents with polycystic ovary syndrome	Alexia Pena	Received

357-P3	A case of Transverse Testicular Ectopia with Persistant Mllerian Duct Syndrome: A novel AMH gene mutation	Suna KILIN	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

358-P3	Argentinean first experience with transgender children and youths	Veronica Figueroa	Received

358-P2	Persistent Mullerian duct syndrome: Rare but important aetiology of an inguinal hernia and cryptorchidism in boys	Abdullah Bereket	Received

359-P3	Long-term follow-up in a Chinese child with lipoid congenital adrenal hyperplasiadue to STARmutation	Xiu Zhao	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

360-P2	SPONTANEOUS PREGNANCIES IN FEMALE SURVIVORS OF CHILDHOOD HEMATOLOGICAL MALIGNANCIES POST ALLOGENEIC HAEMOPOIETIC STEM CELL TRANSPLANTATION	Samantha Lai Ka Lee	Received

361-P2	Towards an integrated approach to diagnosis of 46,XY disorder of sex development.	Zofia Kolesinska	Received

362-P3	Graves Disease in a Pediatric Population: results from the last 17 years at a Pediatric Endocrinology Unit	Ana Antunes	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

363-P2	The human genital tubercle is steroidogenic organ at early pregnancy	Iuliia Savchuk	Received

364-P2	Transgender medicine is a significant part of paediatric endocrinology	Ralph Decker	Received

364-P3	Thyroid Disorders and autoimmunity in Children and Adolescents with Type 1 (T1DM) and type 2 Diabetes mellitus (T2DM)	Ashraf Soliman	Received

365-P3	The Reference and Follow-up Signs and Symptoms of the Cases Who Are Diagnosed as Hyperthyroidism	Ayla Guven	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

366-P3	Clinical Features in Childhood Graves Disease	emine demet akba&351;	Received

366-P2	Genetic etiologies and gender outcomes of patients with disorders of sex development presenting with asymmetric gonads	Arum Oh	Received

367-P3	GENERAL CHARACTERISTICS OF AUTOIMMUNE THYROID DISEASES AND EVALUATION OF ACCOMPANIED MORBIDITIS	BERAY SELVER EKL&304;O&286;LU	Received

367-P2	A rare form of ovotesticular DSD: diagnostic and management challenges	Kruthika Narayan	Received

368-P2	A CASE OF GONADAL DYSGENESIS DUE TO A NOVEL HOMOZYGOUS MUTATION IN NR5A2 GENE	Friederike Denzer	Received

368-P3	Amiodarone induced hyperthyroidism in a pediatric patient	Bernardo Marques	Received

369-P2	Assessment of initial investigation requested in adolescents with menstrual disorders	MARIA CHARAMANTA	Received

370-P2	Persistent Mllerian Duct Syndrome in twin brothers caused by a novel mutation in the AMHR2 gene.	Karolien Van De Maele	Received

370-P3	THYROID CARCINOMA IN CHILDREN. 7 YEARS EXPERIENCE OF A SINGLE CENTER.	Cristina Preda	Received

371-P3	Autoimmune thyroiditis (Hashimoto thyroiditis) in a known case of autoimmune hemolytic anemia	Dina Fawzy	Received

371-P2	Are hypospadias associated with differences in gender role behaviour and sex typical cognitive abilities?	Anna Strandqvist	Received

372-P2	Assessment of the gonadotrophingonadal axis and Sertoli cell function in partial androgen insensitivity syndrome	Doaa Khater	Received

374-P2	EVALUATION OF SERUM ANTI-MULLERIAN HORMONE AND ANDROSTENEDIONE LEVELS IN ADOLESCENTS GIRLS WITH MENSTRUAL IRREGULARITIES	Betul Ersoy	Received

375-P2	Could basal AMH replace hCG stimulation test in patients with XY disorder of sex development?	Shaymaa Mahfouz	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

376-P2	LONG TERM MONITORING OF GRAVES DISEASE IN CHILDREN AND ADOLESCENTS: SINGLE CENTER EXPERIENCE	Selma Tun	Received

377-P2	Effects of Thyroid Autoimmunity on Non-Alcoholic Fatty Liver Disease in Euthyroid Girls with Hashimotos Thyroiditis	Isgven Pinar	Received

377-P3	A Very Rare Thyroid Hormone Resistance Case Having Heterozygous Mutation in THRB Genes	emel hatun aytac kaplan	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

378-P2	The prevalence of clinically significant anti-TPO positivity in children with HLA-conferred susceptibility to type 1 diabetes	Liisa Saare	Received

379-P3	Thyroid Imaging Study for the Diagnosis of Congenital Hypothyroidism with Thyroid Dysgenesis	Jeesuk Yu	Received

379-P2	Encephalopathy Associated with Autoimmune Thyroid Disease: A Case Report	Michael Yafi	Received

380-P3	A Case of permanent congenital hypothyroidism with compound heterozygous mutations in the DUOX2 gene	Jeesuk Yu	Received

380-P2	Celiac disease screening should be routinely offered in pediatric population with autoimmune thyroid disease	Maria Resta	Received

381-P3	Growth catch-up on acquired hypothyroidism presenting with growth delay	Joana Serra-Caetano	Received

381-P2	Autoimmune thyroiditis in Klippel-Feil syndrome with Arnold Chiari and syringomyelia	Elisa Guidoni	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

382-P2	Neonatal monitoring of newborns born from mothers with Graves disease. Results of a retrospective monocentric study.	dominique simon	Received

383-P3	Corticosteroid resistant Immune Thrombocytopenic Purpura, is it a marker of future Graves Disease?	María Cristina Azcona	Received

384-P3	Neonatal hypothyroidism following transplacental amiodarone treatment for supraventricular tachyarrhythmia.	Maria Korpal-Szczyrska	Received

384-P2	Gravess disease during pregnancy: the impact on the fetus and the newborn	Florine Belin	Received

385-P3	Rare case of thyroiditis De Quervain in a six-year-old girl	Maria Liapi	Received

385-P2	Thyroid Hormone Receptor (THRB) mutation: two new cases of heterozygous mutation with significant family history	James Blackburn	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

386-P2	Triac Treatment Response to Thyroid Hormone Resistantance	emine demet akba&351;	Received

387-P2	Phenotype and genotype of four patients with thyroid hormone resistance syndrome due to mutations in the THRB gene	Meropi Toumba	Received

387-P3	Graves disease, Methimazole and SLE-like reaction: A case report	Michael Yafi	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

388-P3	A rare case of pediatric hyperthyroidism	Sara Ciccone	Received

389-P2	A Neurological Disease Mimicking Central Hypothyroidism: MCT8 Deficiency	ozgecan demirbas	Received

389-P3	AllanHerndonDudley syndrome in a patient with Global delay development a case report	shahab noorian	Received

390-P2	Multinodular goiter in childhood: look for DICER1 mutation	Valentine SUTEAU	Received

391-P2	Application of elastography in assesment of different benign thyroid lesions in children and adolescents.	Hanna Borysewicz-Sa&324;czyk	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

392-P2	Clinical Characteristics and Predictive Factors for the Detection of Thyroid Cancer in Children with Thyroid nodules	Junghwan Suh	Received

392-P3	Hashitoxicosis: A rare diagnosis in childhood	Stefanos Stergiotis	Received

393-P3	An assay led astray: a curious case of biotin-induced hyperthyroidism.	Tashunka Taylor-Miller	Received

393-P2	THYROID NODULES IN PRADER-WILLI SYNDROME.	Graziano Grugni	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

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

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

395-P3	Intellectual outcome at childhood in congenital hypothyroidism according to etiology and treatment related factors.	Yong Hee Hong	Received

396-P2	THYROID FUNCTION TESTS AND AFFECTING FACTORS IN TWINS AND TRIPLETS	Zeynep Atay	Received

397-P3	Head Circumference, Birth Length, and Weight of Neonates of Mothers with Hypothyroidism	Zvi Laron	Received

397-P2	Hypothyroidism in a child during treatment with nivolumab for a glioblastoma.	Niels Birkebaek	Received

398-P3	Recombinant growth hormone therapy in prepubertal children with idiopathic short stature in Korea : a phase III randomized trial	Minji Im	Received

398-P2	Amiodarone-induced hyperthyroidism Diagnosis and clinical course in three adolescents	Julia Gesing	Received

399-P2	Allogenic Bone Marrow Transplantation in children: Effect on thyroid function	Elpis Athina Vlachoapapadopoulou	Received

400-P2	Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism	Erdal Kurnaz	Received

400-P3	CLINICAL AND MOLECULAR CHARACTERIZATION OF ONE NR5A1 GENE MUTATION FOUND IN A PATIENT WITH 46, XY DSD	AMAYA VELA	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

401-P2	Clinical management of childhood hyperthyroidism: A longitudinal study at a single center	Tiago Jeronimo dos Santos	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

403-P2	Asymptomatic hyperthyrotropinaemia in children, does it correlate to true thyroid gland dysfunction?	Zacharoula Karabouta	Received

403-P3	Epidemiology, Demographic Criteria and Risk Factors in Type 1 DM Egyptian Children: A Single Center Study	Yomna Shaalan	Received

404-P3	Clinical and biochemical phenotype of aldosterone synthase deficiency	Katharina Foertsch	Received

404-P2	Hearing Loss among Patients with Congenital Hypothyroidism	Tal Almagor	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

406-P3	Two siblings with Prader-Willi syndrome caused by microdeletion derived from the paternal grandmother	Guanping Dong	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

407-P3	DEGLUDEC VERSUS GLARGINE IN PEDIATRIC AND ADOLESCENT PATIENTS WITH TYPE 1 DIABETES	Estela Gil-Poch	Received

408-P3	GENETIC TESTING BY SNP ARRAY ANALYSIS IN A GROUP OF ROMANIAN PATIENTS WITH DISORDERS OF SEXUAL DEVELOPMENT	Diana Miclea	Received

409-P3	A novel gene mutation and atypical clinical phenotype of Kallmann syndrome	Yumiko Terada	Received

409-P2	Do Insulin like Growth Factors also influence growth in children with Congenital hypothyroidism: A cohort analysis	Ruchi Goel	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

410-P2	Study of Hearing function in children with Congenital Hypothyroidism attending Alexandria University Childrens Hospital	Shaymaa Elsayed	Received

411-P2	Awareness of the risks of acquired iodine deficiency in strict Vegan diets	Agnieszka Brandt-Varma	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

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

415-P3	Case Report: Novel ACAN mutation in a SGA short stature without accelerated skeletal maturation	So Eun Park	Received

417-P3	STUDY OF CHILDREN WITH TYPE 1 DIABETES MELLITUS OF LONG DURATION ATTENDING ALEXANDRIA UNIVERSITY CHILDRENS HOSPITAL	Dina Fawzy	Received

418-P3	Clinical and Endocrinological Manifestations of Partial Ectopic Posterior Pituitary: A New Imaging Entity	Marina Ybarra	Received

419-P3	A rare and unexpected cause of diabetes in childhood	Supriyo Basu	Received

57th Annual ESPE Meeting 2018

27 - 29 September 2018 Athens

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DOI: 10.3252/pso.eu.57ESPE.2018



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