EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

58th Annual ESPE Meeting

 

19-21 September 2019 Viena
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N. Poster
Poster title
Applicant name
Status
  RFC13-001 Children and adolescents in the United States with congenital adrenal hyperplasia are not at increased risk for attention-deficit/hyperactivity disorder Lauren Harasymiw Received Received
  RFC11-001 National United Kingdom evidence- and consensus-based guidelines for the investigation, treatment and long-term follow-up of paediatric craniopharyngioma Hoong-Wei Gan Received Received
  RFC10-001 Contemporary surgical approach in CAH 46XX Results from the I-DSD/I-CAH Registries Alexander Springer Received Received
  P2-001 Gender identity, sexual orientation and quality of life in women with non-classic congenital adrenal hyperplasia Anat Segev-Becker Received Received
  RFC7-001 Accuracy of glucose sensor estimate of HbA1c in children with type 1 diabetes Sarah Ehtisham Received Received
  RFC8-001 Trade-off between Olfactory Bulb and Eyeball Volume in Precocious Puberty murat karao&287;lan Received Received
  LB-001 A trial investigating the long-term efficacy and safety of two doses of Norditropin (somatropin; recombinant human growth hormone) in Japanese children with short stature due to Noonan syndrome over four years of treatment Physicians World Europe Received Received
  T-001 Circulating miR-451a: a biomarker to guide diagnosis and treatment of polycystic ovary syndrome in adolescent girls Marta Díaz Received Received
  RFC6-001 EFTUD2 gene deficiency disturbs maturation of osteoblast and inhibits chondrocyte differentiation via activated p53 signaling Jing Wu Received Received
  RFC9-001 Targeted next-generation sequencing for congenital hypothyroidism with positive neonatal TSH screening results Takeshi Yamaguchi Received Received
  RFC12-001 Ovarian follicles of young patients with Turner Syndromecontain normal oocytes but monosomic 45,X granulosa cells Sapthami Nadesapillai Received Received
  P3-001 A case of Cushing syndrome in a Wilms tumour Yvonne Lim Received Received
  RFC5-001 HURTHLE CELL CARCINOMA IN CHILDHOOD: RETROSPECTIVE ANALYSIS OF A LARGE SERIES Giorgia Pepe Received Received
  RFC14-001 Papp-a2 deficiency results in sex-dependent modifications in hypothalamic regulation of energy homeostasis. Jesús Argente Received Received
  P1-001 Could a Glucocorticoid Receptor Polymorphism be Protective against Hypothalamic-Pituitary-Adrenal Axis Suppression in Asthmatic Children on Corticosteroids? Ekkehard Zllner Received Received
  RFC1-001 Low prevalence of maternal microchimerism in Japanese children with type 1 diabetes Kikumi Ushijima Received Received
  RFC3-001 European Registries For Rare Endocrine Conditions (EuRRECa): Results From The Pilot Phase Of The Platform For e-Reporting Of Rare Endocrine Conditions (e-REC) Salma Ali Received Received
  RFC4-002 Circulating Exosomal miRNAs profiles of Childrens Nonalcoholic Steatohepatitis Xuelian Zhou Received Received
  RFC10-002 Cryptorchid boys with abrogated mini-puberty display differentially expressed genes involved in sudden infant death syndrome. Faruk Hadziselimovic Received Received
  P2-002 CYP11A1 (side-chain cleavage enzyme) defect in three brothers causing glucocorticoid and mineralocorticoid deficiency and development of testicular adrenal rest testicular tumour wafa kallali Received Received
  RFC2-002 Does the treatment with recombinant human growth hormone improve final height in patients affected by X-linked hypophosphatemia? JULIA ANDRE Received Received
  P1-002 Software-assisted Analysis of the urinary Steroid Metabolom in treated children with classic Congenital Adrenal Hyperplasia Clemens Kamrath Received Received
  RFC3-002 Factors affecting loss to follow-up in children and adolescents with chronic endocrine conditions: a regional cohort study. Laura ATGER-LALLIER Received Received
  P3-002 A rare cause of primer adrenal insufficiency: NROB1 (DAX1) mutation Ozge Koprulu Received Received
  RFC14-002 Deciphering genetic aetiology among children born small-for-gestational-age with persistent short stature (SGA-SS): Phenotypic characteristics at diagnosis in a large single-centre cohort. Ledjona Toni Received Received
  RFC11-002 Prevalence and predicting factors of endocrine dysfunction in children with NF1 and optic gliomas. Anna Grandone Received Received
  RFC15-002 BMP4 mutations as a novel cause of normosmic hypogonadotropic hypogonadism A. Kemal TOPALOGLU Received Received
  T-002 Assessment of ZnT8 antigen in thyroid cells in children and adolescents with Hashimoto thyroiditis and nodular goitre Hanna Borysewicz-Sa&324;czyk Received Received
  RFC5-002 Ultrasound features of multinodular goiter in DICER1 syndrome Marek Niedziela Received Received
  RFC8-002 Investigation of imprinting alterations in MKRN3 and DLK1 in a cohort of girls with central precocious puberty through specific DNA methylation analysis Ana Canton Received Received
  RFC13-002 Development of novel non-invasive strategies for monitoring of treatment control in patients with congenital adrenal hyperplasia Irina Bacila Received Received
  P2-003 Contraceptives in female adolescents with 21-hydroxylase deficiency (CAH) - a way to optimize treatment with respect to androgen excess? A pilot study. Claudia Boettcher Received Received
  RFC14-003 MicroRNAs change and target key regulatory genes involved in longitudinal growth in patients with idiopathic isolated growth hormone deficiency (IGHD) on growth hormone (GH) treatment Maria Elisabeth Street Received Received
  LB-003 Insights into the regulation of androgen biosynthesis from males with congenital hypogonadotropic hypogonadism: quantification of bioactive steroid hormones reveals differences between gonadotropin replacement and testosterone replacement Julia Rohayem Received Received
  RFC11-003 Polycystic Ovarian Syndrome in Adolescents: Discovery Proteomics and the Search for Novel Non-Invasive Biomarkers Harriet Gunn Received Received
  RFC2-003 Growth hormone effects on metacarpal bone geometry and bone age in growth hormone-deficient children Daniel Zaldumbide Received Received
  P1-003 Simplifying the interpretation of steroid metabolome data by a machine-learning approach tarik kirkgoz Received Received
  RFC10-003 Level of Uncertainty in Diagnostic Evaluation of Boys With XY Disorders of Sex Development (DSD) Malika Alimussina Received Received
  P3-003 A 46, XX patient with 21-OHD diagnosed during the etiologic workup of male infertility. TULAY TULAY Received Received
  RFC12-003 Imprinting defects and copy number variations in short children born small for gestational age Masayo Kagami Received Received
  RFC4-003 Dysregulated gene expression profile in visceral adipose tissue of juvenile Wistar rats with catch-up growth: association with fat expansion and metabolic parameters Judit Bassols Received Received
  T-003 Hypothalamus and Pituitary Gland Antibodies in Childhood-Onset Brain Tumors and Pituitary Dysfunction GIUSEPPA PATTI Received Received
  RFC9-003 NEONATAL SCREENING FOR CONGENITAL HYPOTHYROIDISM: ANALYSIS OF A LARGE COORTE OF AFFECTED PATIENTS (1987-2017) AND RELATIONSHIP WITH PERFLUOROALKYLATED SUBSTANCES (PFAS) IN NORTH-EASTERN ITALY rossella gaudino Received Received
  RFC7-003 Osteopontin as an Early Urinary Marker of Diabetic Nephropathy in Adolescents with Type 1 Diabetes Mellitus Amany Ibrahim Received Received
  RFC8-003 Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5-UTR region of the Imprinted MKRN3 Gene Pavlos Fanis Received Received
  RFC5-003 Experience of thyroid surgery in children with intraoperative neuromonitoring. Alexander Anikiev Received Received
  RFC6-003 Increased burden of common risk alleles in children with a significant fracture history. Despoina Manousaki Received Received
  RFC3-003 The Founder Homozygous NR5A1 Gene Mutation p.R103Q Causes Asplenia and Severe XY-DSD and XX-DSD in a Palestinian Cohort Maha Abdulhadi-Atwan Received Received
  RFC1-003 The Association Between IGF-1 levels and Nonalcoholic Fatty Liver Disease (NAFLD) in Adolescents with Type 2 Diabetes. Jose Antonio Orozco Morales Received Received
  RFC4-004 The novel phosphatidylinositol-3-kinase (PI3K) inhibitor alpelisib effectively inhibits growth of PTEN haploinsufficient lipoma cells. Anna Kirstein Received Received
  RFC5-004 Thyroid dysfunction in patients following thymus transplantation in a tertiary centre: a 10-year experience. Sommayya Aftab Received Received
  P1-004 The Steroidal Milieu in Amniotic Fluid of Mid-Gestation: A Targeted GC-MS Metabolomics Study Rong Wang Received Received
  RFC3-004 Peripheral glucocorticoid metabolim may reflect resolution of inflammation in Kawasaki disease Shuji Sai Received Received
  RFC7-004 Handgrip Strength Correlates with Insulin Resistance and the Metabolic Syndrome in Children and Adolescents: Analysis of the Korean National Health and Nutrition Examination Survey 2014-2016 Hae Woon Jung Received Received
  RFC13-004 Loss-of-function NNT mutations impair antioxidants mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficieny Aline Faccioli Bodoni Received Received
  RFC1-004 ESTIMATION OF MODY FREQUENCY AND PREVALENT SUBTYPES IN PEDIATRIC PATIENTS BY TARGETED NGS Luis Salamanca Received Received
  RFC6-004 Targeted Molecular Genetic Diagnosis by Next Generation Sequence Analysis Method and Investigation of Responsible Candidate Genes in Patients with Osteogenesis Imperfecta Aysun Ata Received Received
  P2-004 Bone age advancement in prepubertal children with premature adrenarche Rita Santos-Silva Received Received
  RFC8-004 Evaluation of puberty in patients with Noonan syndrome and mutations in the RAS/MAPK genes. Alexsandra Malaquias Received Received
  RFC2-004 Bone Mass and Fracture Prevalence in Childhood Brain Cancer Survivors 2, 5 or 7 years after off therapy Annalisa Gallizia Received Received
  RFC10-004 qPCR screening for Xp21.2 copy number variations in patients with elusive aetiology of 46,XY DSD Jakob Meinel Received Received
  RFC11-004 Increased adrenal and testicular androgen concentrations before puberty and in early puberty correlate to adult height outcomes in males with Silver-Russell syndrome Kjersti Kvernebo-Sunnergren Received Received
  P3-004 A female infant with severe salt-wasting due to aldosterone synthase deficiency, initially mimicking adrenal insufficiency Simone Krull Received Received
  RFC9-004 Correlation between Genotype and Phenotype characteristics in Children with Congenital Hyperinsulinism (CHI) in a specialist centre. Laura Bosch i Ara Received Received
  RFC15-004 Clinical and genetic characterization of 153 patients with persistent or transient congenital hyperinsulinism: a population-based study in Finns Jonna Mnnist Received Received
  T-004 Use of stored serum in the study of time trends and geographical differences in exposure of pregnant women to phthalates Louise Scheutz Henriksen Received Received
  RFC14-004 GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon mutation Sumana Chatterjee Received Received
  RFC2-005 Long term effects of treatment with Oxandrolone (Ox) in addition to growth hormone (GH) in girls with Turner syndrome (TS) on bone mineral density in adulthood. Theo Sas Received Received
  RFC4-005 GDF5 Promotes White Adipose Tissue Thermogenesis via p38 MAPK Signaling Pathway Feihong Luo Received Received
  RFC1-005 Decreased circulating levels of MOTS-c in individuals with newly diagnosed type 1 diabetes children Caiqi Du Received Received
  P2-005 Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency. Asmar Aghayeva Received Received
  RFC5-005 A novel mutation in the Thyroglobulin gene leading to Neonatal goiter and Congenital Hypothyroidism in an Eritrean infant Eve Stern Received Received
  RFC14-005 Bioactive IGF-I concentration compared to total IGF-I concentration before and after 1 year of high-dose growth hormone in short children born small for gestational age - North European SGA Study (NESGAS) Rikke Beck Jensen Received Received
  RFC3-005 Evaluation of endothelial function in childhood standard risk acute lymphoblastic leukemia survivors: role of subclinical markers and identification of preventable factors. Patrizia Bruzzi Received Received
  RFC7-005 Dual diagnosis of type 1 diabetes and ADHD Kineret Mazor-Aronovitch Received Received
  RFC8-005 CHD7 mutations in patients with anosmic or normosmic idiopathic hypogonadotropic hypogonadism. Leman Damla KOTAN Received Received
  RFC11-005 IGF-1 serum concentrations and growth in children with congenital leptin deficiency (CLD) before and after replacement therapy with metreleptin Marianna Beghini Received Received
  RFC13-005 Genetics of Familial Glucocorticoid Deficiency over the Decades: Phenotypic Variability and Associated Features Chris Smith Received Received
  LB-005 Height curves and Height SDS in ADHD children measured before and after stimulant treatment are not affected - observation study in 7172 ADHD children Doron Carmi Received Received
  RFC12-005 Cognitive and Neuroradiological assessments in Silver Russell patients GIUSEPPA PATTI Received Received
  P3-005 Can early prenatal prednisone treatment reduce virilization of CAH female newborn? Alessandra Sauna Received Received
  RFC9-005 Spectrum of Neuro-developmental disorders in Children with Congenital Hyperinsulinism due to activating mutations in GLUD1. Sommayya Aftab Received Received
  RFC10-005 Variants in NWD1 gene leading to different degrees of gonadal dysgenesis Odile Christin Gaisl Received Received
  P1-005 18 years of neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: recall rate reduction thanks to liquid chromatograpy-tandem mass spectrometry as second tier test paolo cavarzere Received Received
  RFC8-006 Growth, pubertal course and long-term outcome of 46,XY boys born with atypical genitalia and low birthweight Lloyd Tack Received Received
  RFC15-006 Absence of puberty and estrogen resistance by estrogen alpha receptor inactivation in two sisters: a mutation for variable phenotypic severity Clémence Delcour Received Received
  RFC1-006 An oral trace element supplementation has a potential beneficial effect on glucose homeostasis in transfused patients with -thalassemia major complicated with diabetes mellitus Nancy Elbarbary Received Received
  RFC3-006 Prevalence of endocrine complications in Duchenne muscular dystrophy Primo Kotnik Received Received
  RFC10-006 A mutation in the nucleoporin-107 gene causes aberrant Dpp/BMP signaling and XX gonadal dysgenesis Tikva Shore Received Received
  P2-006 CORTICOSTEROID USE: PRACTICES AND ATTITUDES OF PEDIATRICIANS Yael Lebenthal Received Received
  T-006 Obesity in pediatric age: the analysis of genomic rearrangements Simona Filomena Madeo Received Received
  RFC7-006 Health-Related Quality of Life and Diabetes Control in Immigrant and Italian Children and Adolescents with Type 1 Diabetes and in their Parents. Barbara Predieri Received Received
  RFC14-006 GrowthHormone Deficiency (GHD): Assessing Burdenof Disease in Children and Adolescents: the Growth Hormone Deficiency ChildImpact Measure (GHD-CIM) Meryl Brod Received Received
  P1-006 Health status of children with Congenital Adrenal Hyperplasia due to 21-hydroxylase deficiency in the United Kingdom: results of a multi-centre cohort study Irina Bacila Received Received
  RFC12-006 Exploring the usefullness of a new type of pubertal heigh reference based on growth aligned or onset of pubertal growth. Kerstin Albertsson Wikland Received Received
  RFC4-006 Appetite Suppressing Effects of Glucoregulatory Peptides Devoid of Nausea Christian Roth Received Received
  RFC13-006 Inhibitory effects of Curcuma longa extract on the steroid metabolizing cytochrome P450 enzymes Patricia Rodríguez Castaño Received Received
  RFC6-006 Genetic aetiology predicts growth hormone (GH) treatment outcomes in children born small-for-gestational-age with persistent short stature (SGA-SS). Lessons from a single-centre cohort. Ledjona Toni Received Received
  P2-007 Updates on genotype and phenotype of Vietnamese Patients with X-Linked Adrenoleukodystrophy THU HA NGUYEN Received Received
  LB-007 LONG-TERM EVALUATION OF OVARIAN FUNCTION AND FOLLICULAR RESERVE IN PATIENTS WITH MALIGNANT DISEASES TREATED WITH CHEMOTHERAPY IN PREPUBERTAL OR PUBERTAL AGE Andrea Josefina Arcari Received Received
  P3-007 Rare case of cortisol producing tumour in 14 years old girl. Helena Grskog Received Received
  T-007 A novel Next Generation Sequencing (NGS) panel to facilitate the diagnostic process of X-linked hypophosphataemia (XLH) and other genetic disorders of renal phosphate wasting Susanne Thiele Received Received
  LB-008 Detection of Cardiomyopathy in Egyptian Children and Adolescents with longstanding Obesity using cardiac marker NT-pro PNB and Speckled Tracking Echocardiography Noha Musa Received Received
  P2-008 NOVEL TBX19 MUTATION AS CAUSE OF HYPOGLICEMIA IN TWO SIBLINGS Andrea Castagna Received Received
  T-008 Bone mineral density (BMD) in women with Turner syndrome (TS) from the DSD-LIFE cohort, an epidemiological study Audrey Cartault Received Received
  P3-008 Typical phenotype of isolated aldosterone synthetase (AS) deficiency in two infants with heterozygous AS gene mutation: Dilemma for diagnosis Elif Ozsu Received Received
  P1-008 Follow-up and Prevalence of Precocious Puberty in Children with Classical Congenital Adrenal Hyperplasia diagnosed by Neonatal Screening Veronica Gonzalez Received Received
  LB-009 Left ventricular mass index and cardiovascular function in adolescents born small for gestational age (SGA) Indre Petraitiene Received Received
  P1-009 A Simulation-based Intervention Teaching Illness Management Skills to Caregivers of Children with Adrenal Insufficiency: a Randomised Controlled Study Rebecca Perry Received Received
  P2-009 The clinical polymorphism and variability of X-linked adrenoleukodystrophy in one Russian family. Leila Sozaeva Received Received
  P3-009 Late onset 11 Beta Hydroxylase Deficiency: Two cases Elvan Bayramoglu Received Received
  T-009 Empagliflozin And GABA Improve &946;-Cell Mass And Glucose Tolerance In Streptozotocin-Treated Mice Sophie Welsch Received Received
  P3-010 An unusual Testicular Adrenal Rest Tumor localization in a 15-year-old boy with congenital adrenal hyperplasia. Domenico Corica Received Received
  T-010 Changes in adrenal androgens and steroidogenic enzyme activities in children aged 2, 4, and 6 years: Steroid hormone profiling from the prospective cohort study Jae Hyun Kim Received Received
  P1-010 Global Practice of Glucocorticoid and Mineralocorticoid Treatment in Children and Adults with Congenital Adrenal Hyperplasia Insights from the I-CAH Registry Irina Bacila Received Received
  P2-010 Functional adrenocortical oncocytoma a rare cause of progressive virilization and secondary amenorrhea Katja Dumic Kubat Received Received
  P1-011 ASSESSMENT OF THE ADRENAL FUNCTION IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA BEFORE AND AFTER INDUCTION THERAPY WITH CORTICOSTEROIDS doaa khater Received Received
  LB-011 Height in Inborn Errors of Metabolism requiring hypoprotidic diet: a longitudinal follow up study about 213 patients kanetee Busiah Received Received
  P3-011 Primary Adrenal insufficiency in Sudanese children (clinical presentation, etiology and diagnostic challenges) Salwa Elhassan Received Received
  T-011 Droplet Digital PCR Techniques to detect R201 mutations in the Mccune-Albright Syndrome wenli Lu Received Received
  P2-011 Long-term Prednisone versus Hydrocortisone Treatment in Children with Classic Congenital Adrenal Hyperplasia (CAH): A Controlled Study Shayma Elsayed Received Received
  P1-012 Trientine treatment mimicking severe hyperandrogenism Gerhard Binder Received Received
  P2-012 A case of X-linked adrenoleukodystrophy presenting with primary adrenal insufficiency and normal VLCFA Beyhan zkaya Received Received
  T-012 The first description of large pathogenic deletion in ACAN gene and additional cases with novel pathogenic ACAN variants Lana Stavber Received Received
  P3-012 Clinical follow-up of a novel NR0B1 mutation in a case of Adrenal Hypoplasia Congenital?? Haihua Yang Received Received
  LB-012 Thyroid function in neonates conceived after hysterosalpingography with iodinated contrast media Nienke van Welie Received Received
  LB-013 Gut hormones secretion across clusters of Metabolic Syndrome in obese prepubertal children Nella Polidori Received Received
  T-013 Results from the implementation of a 2 year growth awareness and growth disorders screening campaign (GrowInform) Kaloyan Tsochev Received Received
  P1-013 Cytokines and the impairment of puberty Natalia Shlyachova Received Received
  P3-013 Genotype and phenotype, growth outcome in 33 Korean patients with 21-hydroxylase deficiency Ju Young Yoon Received Received
  P2-013 Different Potent Glucocorticoids, Different Routes of Exposure but The Same Result: Iatrogenic Cushings syndrome and Adrenal Insufficiency Ayla Guven Received Received
  LB-014 Prenatal smoke-exposure is associated with increased anogenital distance in female infants Deniz zalp Kizilay Received Received
  P3-014 One case report of Uighur girl with Cushing syndrome wenjing li Received Received
  P2-014 Differences between normal-BMI girls with Premature Adrenarche and overweight or obese girls with Premature Adrenarche Rita Santos-Silva Received Received
  T-014 The Effect of Endocine Disrupting Chemicals to Precocious Puberty in Children with Exposure History of Slim Jung Eun Moon Received Received
  P1-014 Refractory hypercalcemia after Denosumab treatment in pediatric age: a case report annalisa deodati Received Received
  T-015 Intestinal microbiota development differs between pubertal boys and girls Sampo Kallio Received Received
  P1-015 The overweight and obesity decrease the growth potential in Mexican children and adolescents. América Liliana Miranda - Lora Received Received
  LB-015 Efficacy of 3-Monthly Compare to Monthly Depot GnRH agonist (Triptorelin Pamoate) in the treatment of girls with Central precocious puberty in Korea Lindsey Yoojin Chung Received Received
  P3-015 Nephrotic Syndrome Developed in a Girl With Lipoid Adrenal Hyperplasia due to StAR gene mutation First Report Kyung Mi Jang Received Received
  P2-015 Rare Causes of Primary Adrenal Insufficiency at King Faisal Specialist Hospital -Retrospective Study Mohammed Alotaibi Received Received
  T-016 IGF2 Mutations: Report of Six Japanese Cases and Phenotypic Comparison with H19/IGF2:IG-DMR Epimutations including literature cases Yohei Masunaga Received Received
  P3-016 Pneumocystis Jiroveci pneumonitis complicating neonatal Cushings syndrome - the therapeutic dilemma Adi Auerbach Received Received
  P2-016 A Case of Infantile Cushings Syndrome from McCune Albright Syndrome: The Importance of Multiple-Site Sampling for Genetic Testing Nicholas Beng Hui Ng Received Received
  P1-016 Normocalcemic Hyperparathyroidism in Children DIMITRIOS PAPADIMITRIOU Received Received
  P3-017 Newborn screening for congenital adrenal hyperplasia: should we worry more about false positives or false negatives? Sara Ciccone Received Received
  P2-017 Duodenal web presenting as pseuhypoaldosteronism in infancy. Mireille El Bejjani Received Received
  T-017 FACTORS ASSOCIATED WITH DYSLIPIDEMIA IN PATIENTS WITH TYPE 1 DIABETES: A SINGLE-CENTER EXPERIENCE Sari Krepel Volsky Received Received
  LB-017 Assessment of Urinary Podocalyxin as a Marker of Glomerular Injury in Obesity Related Kidney Disease in Obese Children and Adolescents compared to urinary Albumin-creatinine ratio Noha Musa Received Received
  P1-017 SERUM TESTOSTERONE LEVEL AT THE AGE OF 12 IS AN IMPORTANT DETERMINANT OF THE FOLLOWING GAIN OF BONE MINERAL APPARANT DENSITY IN 18-YEAR OLD MALES: A LONGITUDINAL STUDY FROM PUBERTY. Vallo Tillmann Received Received
  LB-018 Exploratory case-control study on ACE2 expression in children with short stature Gianluca Tornese Received Received
  T-018 Early treatment with intravenous bisphosphonates prevents severe postnatal bone loss in children with Osteogenesis imperfecta Mirko Rehberg Received Received
  P1-018 Nephrocalcinosis in children with X-Linked Hypophosphatemia: prevalence and risks factors Mathilde Grapin Received Received
  P2-018 A rare case of pseudohypoaldosteronism in a neonate secondary to congenital hydrometrocolpos Shruti Kumar Received Received
  P3-018 The unusual adverse side effects of super-potent topical steroids. Yasmine Abdelmeguid Received Received
  LB-019 CDX2 polymorphism of VDR gene and lipid profile in patients treated for acute lymphoblastic leukemia during childhood. Ewa Barg Received Received
  P2-019 Hyperandrogenism in a 13-year-old girl due to glucocorticoid receptor mutation Osnat Admoni Received Received
  T-019 Urinary Gonadotrophins in Girls with Turner Syndrome Alessandra Boncompagni Received Received
  P3-019 A case with central adrenal insufficiency and early onset obesity: Proopiomelanocortin deficiency Sezer Acar Received Received
  P1-020 Long-term Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism Raffaele Buganza Received Received
  P3-020 Short Synacthen Test in Children at Sultan Qaboos University Hospital; Reviewing the sampling times Hussain Alsaffar Received Received
  T-020 Molecular and phenotypicspectrum of Noonan syndrome in Chinese patients Xin Li Received Received
  P2-020 Polydipsia, hyponatremia and a biochemical profile of aldosterone synthase deficiency Christina Reinauer Received Received
  LB-020 Introduction of flash glucose monitoring in children with Type 1 diabetes: experience of a single-centre in Spain Robert Brines Received Received
  P1-021 Dual X-ray Absorptiometry in Children With Hypophosphatasia Treated with Asfotase Alfa: a Pooled Post Hoc Analysis Gabriel Á. Martos-Moreno Received Received
  P3-021 Pheochromocytoma in children: a case report Thanh Nguyen Trong Received Received
  P2-021 Fludrocortisone treatment in a child with Postural Orthostatic Tachycardia Syndrome (POTS): a case report. Gaia Varriale Received Received
  P3-022 A Case with Congenital Adrenal Hyperplasia Diagnosed by Malnutrition emine demet akba&351; Received Received
  LB-022 TWO NOVEL MUTATIONS OF THE LHX3 GENE ASSOCIATED WITH A SEVERE PHENOTYPE INVOLVING ENDOCRINE, NERVOUS AND SKELETAL SYSTEMS LAURA GUAZZAROTTI Received Received
  P1-022 Differences in bone strength and cortical bone parameters in young Swedish women with Type 1 diabetes Eva Kristiansen Received Received
  LB-023 Long-term safety and effectiveness of recombinant human growth Hormone in Korean pediatric patients with growth disorders: 7-year interim analysis from LG Growth Study Young Ah Lee Received Received
  P3-023 Recurrent Hypoglycemia-Not every low sugar is hyperinsulinemia DEEPTI CHATURVEDI Received Received
  P1-023 INCREASED PREVALENCE OF OVERWEIGHT AND OBESITY AND ITS CLINICAL PREDICTORS IN CHILDREN AFFECTED BY X-LINKED HYPOPHOSPHATEMIA VOLHA ZHUKOUSKAYA Received Received
  P2-023 Girls with idiopathic premature adrenarche achieve normal adult height. Leandro Soriano-Guillén Received Received
  LB-024 Abdominal adiposity and total body fat as predictors of cardiometabolic health in pre-pubertal and pubertal youth BInghan Jin Received Received
  P2-024 Adult height and growth pattern in patients with classic congenital adrenal hyperplasia Ga Hyun Lee Received Received
  P1-024 Novel Homozygous LRP5 Mutations in Patients with Osteoporosis-Pseudoglioma Syndrome Fatemeh Saffari Received Received
  P3-025 Unusual association : Allgrove syndrome and hypopituitarism Mouna Mnif Feki Received Received
  LB-025 Low Trabecular Bone Score in Children with Inflammatory Bowel diseases Yael Levy Shraga Received Received
  P2-025 Cushing Syndrome due to an adrenacortical carcinoma in a baby with atypical Beckwith-Wiedemann Syndrome eltan mehmet Received Received
  P1-025 Pathogenicity of GCK gene mutation c.364CG (p.Leu122Val) David Crudo Received Received
  P2-026 Successful Parathyroidectomy with Intraoperative Parathyroid Hormone Monitoring in a Neonate with Severe Primary Hyperparathyroidism Caused by Homozygous Mutation in CASR Kinnaree Sorapipatcharoen Received Received
  P1-026 Myocardial function in asymptomatic children with type 1 diabetes hager barakizou Received Received
  LB-026 Dramatic clinical response to Lenvatinib in one pediatric patient with advanced metastatic papillary thyroid carcinoma Noelia Dujovne Received Received
  P3-026 Title: Long-term outcome of congenital adrenal hyperplasia patients at KFSHRC-Saudi Arabia. Tertiary Center Experience Haneen Aldalaan Received Received
  P3-027 A boy with adrenal hypoplasia congenita without external genital abnormalities Ikumi Umeki Received Received
  LB-027 Does karyotyping and in situ hybridization from three different germ layers elucidate low bone mineral density in Turner syndrome? Ondrej Soucek Received Received
  P2-027 The First Case Report of SEMD-JL1 in China ke Huang Received Received
  P1-027 A Case of Neonatal Diabetes with Hyperferritinemia: A Distal PTF1A Enhancer Mutation Glin Arslan Received Received
  P1-028 Elevated anti-tissue transglutaminase antibodies in children newly diagnosed with type 1 diabetes do not always indicate celiac disease AHU PAKET&304; Received Received
  LB-028 The Volumetric Changes in the Olfactory Bulb Depend on Body Mass Index murat karao&287;lan Received Received
  P3-028 Linear growth in Children with COW Milk allergy and their response to hypoallergenic diet; Significant Catch-up in the first 6 months. Ashraf Soliman Received Received
  P1-029 What hypoglycemia does to the heart: Impact of nocturnal hypoglycemia on cardiac repolarization in diabetic children. Sara Bachmann Received Received
  P2-029 Clinical and Genetic Characteristics of Pseudohypoparathyroidism Type 1A in Children Based on Single-center Cohort Study Xuelian Zhou Received Received
  P3-030 ENPP1 hypophosphatemic rickets in a 3.6 years old Italian child Daniele Tessaris Received Received
  P1-030 Effects of Glypican-4 Protein on INS1E Cell Viability and Insulin Signaling Joseph Buhl Received Received
  P2-030 A rare case of neonatal hypocalciuric hypercalcemia complicated with arrhythmia Yuto Arai Received Received
  P2-031 Experience of burosumab therapy for 6 months in four children with X-linked hypophosphataemic rickets in Saudi Arabia Fahad Al-Juraibah Received Received
  P3-031 A case study of X-linked hypophosphataemia: The effect of conventional therapy from childhood to adulthood in Saudi Arabia Afaf Al-Sagheir Received Received
  P2-032 Pediatric patients with heterozygous ALPL mutation show a broad clinical phenotype Corinna Melanie Brichta Received Received
  P1-032 Heterozygous RFX6 mutation as a cause of diabetes mellitus in a multigenerational family Nehama Zuckerman Levin Received Received
  P2-033 Growth and Bone Mineral Density in Egyptian Children with Congenital Adrenal Hyperplasia on Glucocorticoid Replacement Therapy; A Single Center Study Omar Magdy Omar Received Received
  P3-033 In case of osteogenesis imperfecta transmission in pregnancy: check vitamine D and calcium status of the mother. Valerie PORQUET-BORDES Received Received
  P2-034 Chronic Bone Disease in Pediatric Sickle Cell Disease Including a Case of Successful Bisphosphonate Therapy Chelsey Grimbly Received Received
  P1-034 Serum Dipeptidyl peptidase-4 Activity and its Relation to Insulin Resistance in Type 1 Diabetic Adolescents Amany Ibrahim Received Received
  P1-035 The impact of CGM availability: real world data from a population based clinic Elaine Sanderson Received Received
  P3-035 Pseudohypoparathyroidism: Four cases reports Marina Bressiani Received Received
  P2-035 Clinical and genetic characteristics of 168 Russian patients with hypophosphatemic rickets Kristina Kulikova Received Received
  P1-036 Expression of receptor for advanced glycation end-products and its ligands HMGB1 and s100A12 in children and adolescents with new-onset Type 1 diabetes and in patients with longer disease duration Anita Spehar Uroic Received Received
  P2-036 A 10-year-old girl with primary hypoparathyroidism and systemic lupus erythematosus (SLE) Hanna Borysewicz-Sa&324;czyk Received Received
  P3-036 A Case of Robinow syndrome Huseyin Anil Korkmaz Received Received
  P2-037 An unusual case of hyperparathyroidism: familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) associated with mutations in CLDN19 Yuezhen Lin Received Received
  P1-037 Association of maternal depressive symptoms with worse metabolic control in adolescents with Type 1 Diabetes Hernan Garcia-Bruce Received Received
  P1-038 The factors associated with high levels of HbA1C in children and young people with Type 1 Diabetes mellitus Omolola Ayoola Received Received
  P3-038 Mild Hypophosphatasia in a Family with a Novel Mutation in the ALPL gene YONG HEE HONG Received Received
  P2-038 Skeletal Maturity and Growth in children with Type 1 diabetes Nikhil Lohiya Received Received
  P2-039 Bone mineral status in adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency imen gargouri Received Received
  P1-039 Differences between short- and long-term outcomes of laparoscopic sleeve gastrectomy in adolescence Marina Ybarra Received Received
  P3-039 UNCOMMON ASSOCIATION OF HYPOPARATHYROIDISM AND RENDU-OSLER SYNDROME MIRELA IANCU Received Received
  P3-040 Barakat Syndrome (HDR Syndrome): Case Report Marina Bressiani Received Received
  P2-040 REDUCED BONE MINERAL DENSITY IN CHILDREN WITH INFLAMMATORY BOWEL DISEASE WITHOUT EXPOSURE TO CORTICOSTEROID TREATMENT Feneli Karachaliou Received Received
  P2-041 A clinical dilemma in the detection of paediatric hypophosphataemia Clement Ho Received Received
  P1-041 Growth arrest-specific 6 (Gas6) protein is associated with adiposity and metabolic syndrome in obese children and adolescents Daniel Zaldumbide Received Received
  P3-041 Myelofibrosis in Severe Vitamin D Deficiency Rickets: A Case Report Omar Magdy Omar Received Received
  P3-042 Congenital Hyperinsulinism in Kosova Vjosa Mulliqi Kotori Received Received
  P3-043 About a case of neonatal hypocalcemia Gilda Belli Received Received
  P1-043 Association of biomarkers of endothelial dysfunction with MicroRNAs levels in overweight and obese adolescentes Fengyang Huang Received Received
  P2-043 A rare form of Vitamin D Receptors dysfunction (vitamin D-dependent rickets type II) with alopecia. A Case Report Shayma Osman Received Received
  P2-044 Cinacalcet experience in hypercalcemia due to CaSR mutation Esra Dger Received Received
  P3-045 Acute Lymphoblastic Leukemia;Atypically Presenting with Sever Hypercalcemia in a Palestinian Child HASAN EIDEH Received Received
  P1-045 Non-Alcoholic Fatty Liver Disease and eGFR levels could be linked by the PNPLA3 I148M polymorphism in obese children ANNA DI SESSA Received Received
  P2-045 Two siblings with hypophosphatemic rickets: SLC34A3 gene mutations with different clinical phenotypes Esin Karakilic Ozturan Received Received
  P2-046 Seasonal 25-hydroxy Vitamin D3 variations in school-aged children from Santiago de Chile Helena Poggi Received Received
  P3-046 Growth hormone treatment of a patient with X-linked hypophosphatemic rickets caused by PHEX mutation: effects on linear growth Aleksandra Rojek Received Received
  P1-048 Waist circumference triglyceride index is useful to predict non-alcoholic fatty liver disease in childhood obesity. Bahar zcab&305; Received Received
  P3-048 Oral Glucose Tolerance Test (OGTT) as a useful tool for early diagnosis of Type 2 Diabetes Mellitus and prediction of metabolic risks in children and adolescents. Eirini Kostopoulou Received Received
  P3-049 Significance of the Early Marker of Nephrine Diabetic Nephropathy of the Uzbek Nationality with the First Type of Diabetes Mellitus. Ziyoda Rakhimberdieva Received Received
  P2-049 Successful treatment with enzyme replacement therapy in a girl with severe infantile Hypophosphatasia Katrin Heldt Received Received
  P1-049 Gut Microbiome of North-American Children with and without Prader-Willi Syndrome (PWS) Andrea Haqq Received Received
  P3-050 Hybrid diabetes with good response to metformin in an Adolescent with polyglandular polyendocrinopathy (APS2) noor Hamed Received Received
  P2-050 Bone Mineral Density in Children with Type 1 Diabetes Mellitus (T1DM) and Analysis of Possible Factors Affecting Their Bone Health; A controlled study. Shayma Elsayed Received Received
  P1-051 Pathogenic mutations and variants in KSR2 in a cohort of obese children Ingrid Krber Received Received
  P2-051 Perinatal form hypophosphatasia caused by a novel large duplication of ALPL gene and two year follow-up under enzyme replacement therapy; a case report Bulent Hacihamdioglu Received Received
  P3-052 Off label use of CGM in a pediatric patient with type 1 Diabetes Mellitus under the age of 2 Liliana Burdea Received Received
  P1-052 EFFECT OF FEEDING MODE ON LONGITUDINAL BODY COMPOSITION IN EARLY LIFE Kirsten de Fluiter Received Received
  P2-052 A rare cause of hypophosphatemia: Raine Syndrome mehmet eltan Received Received
  P3-053 A case of congenital hyperinsulinism due to ABCC8 mutation: A challenge to diagnosis, management, and treatment Zacharoula Karabouta Received Received
  P2-053 Idiopathic infantile hypercalcemia: Mutations in SLC34A1 and CYP24A1 in two siblings and fathers Ayla Guven Received Received
  P1-053 Age of obesity onset could be the first indicator of future metabolic complications preliminary data of prospective multicenter study Aneta Gawlik Received Received
  P1-054 Augmented Fibroblast Growth Factor 21 Serum Levels in Metabolic Disorders and Association With Endothelial Function in Childhood Eleni Domouzoglou Received Received
  P3-054 Relationship between Chloride infusion and Base Excess in initial treatment of pediatric diabetic ketoacidosis Kentaro Sawano Received Received
  P1-055 A novel recurrent heterozygous PLIN1 mutation in three Russian patients with partial lipodystrophy, dyslipidemia and insulin resistance. Yulia Tikhonovich Received Received
  P2-055 A novel missense COL10A1mutation identified by next generation sequencing in a Chinese pedigreewith Schmid metaphyseal chondrodysplasia Qiong Chen Received Received
  P3-055 The role of patient adherence to insulin pump therapy with long-term treatment of type 1 diabetes Mariia Turkunova Received Received
  P2-056 a case report of a girl with short stature has laron syndrome and spondyloepimetaphyseal dysplasia Abdullah Alshahrany Received Received
  P3-056 Long-term honeymoon period in Type 1 diabetes: True diagnosis MODY5; New mutation of HNF1B Esra Dger Received Received
  P1-056 Carotid intima-media thickness relates to epicardial and perirenal fat rather than to total body adiposity in apparently healthy children Abel López Bermejo Received Received
  P2-057 A NOVEL MUTATION OF PHEX GENE INDUCING X-LINKED HYPOPHOSPHATEMIA RICKETS, A CASE REPORT RENATA PINTO Received Received
  P3-057 Prevalence of Celiac disease (CD) and autoimmune thyroid dysfunction (AITD) in Indian children with Type 1 Diabetes Vasundhara Chugh Received Received
  P1-057 Put your money where your mouth is: preliminary evidence that oral microbiota diversity may shape later cardiometabolic health in children Melanie Henderson Received Received
  P2-058 Skeleton muscles and tissues metabolic activity in Greek adolescent PCOS Styliani Geronikolou Received Received
  P1-058 A case-control study of exposure to bisphenol-A and phthalates in obese children annalisa deodati Received Received
  P2-059 SPONDYLOOCULAR SYNDROME: PRESENTATION OF TWO SIBLINGS DIAGNOSED WITH THE RARE DISEASE AND THE RESULTS OF PAMIDRONATE THERAPY Yagmur Unsal Received Received
  P1-059 Growth patterns in non-syndromic childhood overweight: comparing children with early of late onset weight gain Alina German Received Received
  P2-060 Clinical and Genetic Characterization of Tunisian Children with Hereditary Hypophosphatemic rickets (HHR). Selmen Wannes Received Received
  P2-061 Osteogenesis Imperfecta: Genetic evaluation Lidia Castro-Feijoo Received Received
  P3-061 The Effect of Fibroblast Growth Factor 23 on Serum Phosphorus Level in Children with Diabetic Ketoacidosis Hakan Doneray Received Received
  P2-062 The Effect of Carbohydrate Recognition and Counting Ability on Glycemic Control in Pediatric Patients with Type 1 Diabetes Minutti Carla Received Received
  P3-062 What does the insulin pump change in children with type 1 diabetes? One-year clinical follow-up Ilknur Arslanoglu Received Received
  P3-063 Severe heart disease can cause diabetes mellitus even in younger age: Case reports of two Japanese adolescent boys. Yukie Izumita Received Received
  P1-063 Altered gut microbiota in Obese children: sex-associated signature Ruimin Chen Received Received
  P2-063 A Rare Case of Syndromic Diabetes due to an INSR pathogenic variant Tara Tayeb Received Received
  P1-064 Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome. Louise Sonia Received Received
  P2-064 Autoimmune thyroid diseases in children and adolescents with Maturity Onset Diabetes of the Young Valeria Calcaterra Received Received
  P3-064 De novo mutation of ABCC8 gene in a child with MODY developed at 25 months of age Jeesuk Yu Received Received
  P1-065 Congenital Hyperinsulinism Due to Pancreatic Mosaicism for Paternal Uniparental Disomy of all Chromosome 11, with the Additional Finding of Pancreatic Mosaicism for Trisomy 12. Louise Conwell Received Received
  P3-065 Insulin-induced oedema in a child with newly diagnosed diabetes mellitus Meltem Didem cakir Received Received
  P1-066 Salivary free cortisol measurement: A diagnostic Approach to assess adrenal failure in symptomativ premature patients Felix Reschke Received Received
  P2-066 New mutation of the PDX-1 gene causes MODY Type 4 diabetes in a 17 year old girl with good response to oral antidiabetics SOFIA GIATROPOULOU Received Received
  P3-067 WHAT HAS CHANGED IN TYPE 1 DIABETES MELLITUS CASES IN THE LAST EIGHT YEARS? A SINGLE CENTER EXPERIENCE MUSTAFA KEND&304;RC&304; Received Received
  P1-067 Screening of congenital hypothyroidism using umbilical cord blood in a maternity hospital Clement Ho Received Received
  P3-068 Seasonal variation and epidemiological parameters in children from Western Greece with Type 1 Diabetes Mellitus (T1DM). Eirini Kostopoulou Received Received
  P2-068 Pancreatic Cell Function and its relationship with iron overload in Patients with -Thalassemia Major Lina ZHANG Received Received
  P3-069 An 8-year-old boy with Down syndrome who has had a history of transient hyperinsulinemia and was found to have type 1 diabetes during ALL treatment Naoko Nishimura Received Received
  P2-069 Gluten-free diet in children with recent onset type 1 diabetes is associated with slower pace of C-peptide decline and better metabolic control at 12 months Vít Neuman Received Received
  P2-070 Evaluation of -cell function in young MODY patients using a Mixed Meal Tolerance Test Ingrida Stankute Received Received
  P3-070 Indicators of Caries Risk in Children with Type 1 Diabetes Mellitus Ehsan Mowafy Received Received
  P1-070 Congenital Hypothyroidism Precise Diagnosis with Dual Imaging ramona nicolescu Received Received
  P3-071 Vitamin D status in Egyptian children with newly-diagnosed type 1 Diabetes and its relation to autoimmune destruction of pancreatic beta cells Wafaa Laymoun Received Received
  P1-071 Clinical, biochemical and echocardiographic evaluation of patients with congenital rickets due to maternal vitamin D deficiency Huseyin Demirbilek Received Received
  P2-071 The Effect of Different Forms of Maternal Dysglycemia on the occurrence of Neonatal Hypoglycemia in babies admitted to NICU. Ashraf Soliman Received Received
  P1-072 Diagnostic value of random serum growth hormone (GH), IGF-I and IGFBP-3 concentrations for the diagnosis of growth hormone deficiency (GHD) in patients below one year of life. María Gabriela Ballerini Received Received
  P3-072 Hematologic indices indicating platelets activity in children with type 1 diabetes setila dalili Received Received
  P2-072 ADROPIN, AFAMIN AND NEUDESIN - NOVEL BIOMARKERS OF TYPE 1 DIABETES MELLITUS IN CHILDREN Agnieszka Polkowska Received Received
  P2-073 Prevalence, Time trend and predictors of Celiac Disease in Type 1 Diabetes neha agarwal Received Received
  P1-073 Influence of birth parameters on growth response and metabolic effects of growth hormone (GH) therapy in GH-deficient children and adolescents Ewelina Witkowska-S&281;dek Received Received
  P3-073 THE PREVALENCE OF HYPERTENSION AND ITS RELATIONSHIP TO GLYCEMIC CONTROL IN CHILDREN WITH TYPE 1 DIABETES MELLITUS doaa khater Received Received
  P3-074 Does metformin therapy prolong the honeymoon period in obese adolescent with hybrid diabetes? Noor Hamed Received Received
  P1-074 RECOMBINANT GH TREATMENT IN CHILD WITH PSEUDOPSEUDOHYPOPARATHYROIDISM ASSOCIATED WITH GROWTH HORMONE DEFICIENCY Feneli Karachaliou Received Received
  P2-074 IMPACT OF THE FLASH GLUCOSE MONITORING SYSTEM ON CHILDREN WITH TYPE 1 DIABETES AFTER THE FIRST YEAR OF USING IN SYSTEMATIC WAY Concepcion Freijo Received Received
  P2-075 Impact of Insulin treatment of Cystic Fibrosis Related Diabetes (CFRD) on BMI and respiratory function Manuela Caruso-Nicoletti Received Received
  P1-075 Impact of -202 IGFBP-3 Promoter Polymorphism on Growth Responses in Korean Children with Idiopathic Short Stature Seung Yang Received Received
  P1-076 The Diagnostic Value of Serum Acid-labile Subunit (ALS) alone and in combination with IGF-1 and IGFBP-3 in the diagnosis of Idiopathic Growth Hormone Deficiency (iGHD) Jiajia Chen Received Received
  P2-076 Coexistence of Medium chain acyl-CoA dehydrogenase deficiency (MCADD) and Type 1 diabetes (T1D): A management challenge Donald Afreh-Mensah Received Received
  P3-076 Extra attention to be paid when looking after boys with Type 1 Diabetes Mellitus in Oman Hussain Alsaffar Received Received
  P3-077 Factors affecting the preservation of C-Peptide Secretion in Egyptian children with Type 1 Diabetes Amany El-hawary Received Received
  P1-077 Severe IGF-I deficiency in children with normal growth hormone (GH) secretion and excluded GH insensitivity is it really idiopathic short stature? Joanna Smyczynska Received Received
  P2-077 Education in type 1 diabetes mellitus (T1D): what do educators really know? A tunisian multicenter study among young doctors, nurses and nutritionnists wafa kallali Received Received
  P2-078 A case of an infant with congenital hyperinsulinism complicated by diabetic ketoacidosis during treatment CHAERI YOO Received Received
  P3-078 Prevalence of Fatty Liver in Children with Type 1 Diabetes Mellitus Attending Diabetes Clinic of Alexandria University Childrens Hospital Ehsan Mowafy Received Received
  P1-079 The experience of pain in children with Growth Hormone deficiency and psychosocial correlates: preliminary data from a longitudinal prospective study. Alessandra Bettini Received Received
  P1-080 Clinical characteristics, puberty pattern and adult or near-adult-height data in a group of patients with growth failure due to severe primary IGF-1 deficiency (GROWPATI study) athanasia stoupa Received Received
  P2-080 Effect of multiple dose insulin on glycaemic control and adiposity in children and adolescents with type 1 diabetes; a Sri Lankan experience Raihana Hashim Received Received
  P3-080 A Real-Life Experience with A New Insulin Co-Formulation Degludec/Aspart For One Year In Poorly Controlled Children And Adolescents With Type 1 Diabetes serap turan Received Received
  P3-082 Assessment of testicular volume by Ultrasound in Children and Adolescents with Type 1 diabetes Nikhil Lohiya Received Received
  P2-082 Thiamine responsive megaloblastic anemia syndrome with restrictive cardiomyopathy: a case report Wafaa Laymoun Received Received
  P1-082 Positive impact on adherence through educational activities of the Argentinas Patient Support Program in children with low adherence to treatment with recombinant Growth Hormone (easypod applicator). Cinthia Chareca Received Received
  P3-083 Diabetes mellitus in a 16-year-old boy developing multiple neuro-endocrine dysfunctions in the course: Is it type 1 diabetes or Wolfram syndrome, or both? Maristella Santi Received Received
  P2-083 17q12 Deletion and a Family History of Diabetes ramona nicolescu Received Received
  P1-083 Identification of novel recessive IGFALS mutations and INSR variant in an obese Korean boy Yoo-Mi Kim Received Received
  P1-084 Development of a parent experience measure forparents of children with achondroplasia Jane Beck Received Received
  P3-084 A low-carbohydrate diet improves metabolic control in a type 1 diabetic child without side effects Philippe Klee Received Received
  P2-084 An Unusual Presentation of Type 1 Diabetes faisal alwadiy Received Received
  P1-085 BONE MINERAL DENSITY IS NORMAL IN PREPUBERTAL PATIENTS WITH TURNER SYNDROME WHEN CORRECTED BY HEIGHT/AGE Sofia Helena Valente Lemos-Marini Received Received
  P2-085 Clinical characteristics and treatment outcomes in patients with autoantibody-negative ketosis-prone diabetes Shin-Hee Kim Kim Received Received
  P3-086 Clinical profile of paediatric patients with type 1 diabetes mellitus at a tertiary health care center in the oriental region of northeastern Morocco Salma Benyakhlef Received Received
  P2-086 Factors influencing the formation and support of the motivation to self-control of adolescents with type I diabetes mellitus Olena Kyrylova Received Received
  P1-086 Extreme short stature and poor pubertal growth: when FBN1 is the culprit Cécile Brachet Received Received
  P3-087 Comprehensive Analysis of HLA System Class II DRB1 in children with Insulin Dependent Diabetes Mellitus in the North Azerbaijan and Iranian Azerbaijan Gunduz Ahmadov Received Received
  P2-087 Glycemic Control in Egyptian Adolescent Girls with Type 1 DM yomna shaalan Received Received
  P3-088 A case of Type 2 diabetic adolescent with sleep apnea who was successfully stopped metformin after adenotonsillectomy Ji-Young Seo Received Received
  P2-088 A qualitative study investigating the experiences of using Solution Focused Therapy in a paediatrics diabetes team. Mark Guyers Received Received
  P1-088 Etiology of Severe Short Stature: Single Center Experience Matti Hero Received Received
  P1-089 Clinical Outcomes in Primary Empty Sella (ES) Syndrome in Childhood-Onset Growth Hormone Deficiency: Data from KIGS (Pfizer International Growth Database). Michael Wajnrajch Received Received
  P3-089 A mitophagic response to iron overload-induced oxidative damage associated with the PINK1/Parkin pathway in pancreatic beta cells Lina ZHANG Received Received
  P2-090 NEONATAL DIABETES IN TWO SIBLINGS WITH FOXP3 VARIANT MARIA CAROLINA COLOMBI GONZALEZ Received Received
  P3-091 Association of type 1 diabetes and celiac disease in child Daniel Zaldumbide Received Received
  P1-091 Ectopic posterior pituitary, polydactyly, midfacial hypoplasia and panhypopituitarism due to a novel heterozygous IVS11-2AC(c.1957-2AC) mutation in GLI2 gene edip unal Received Received
  P2-091 A novel variant of the WFS1 gene with dominant inheritance causing Wolfram-like syndrome Juraj Stanik Received Received
  P2-092 AN IMPAIRED LIPID PROFILE IS A SIGN OF REDUCED INSULIN SENSITIVITY IN CHILDREN AND ADOLESCENTS AT TYPE 1 DIABETES ONSET Giulio Maltoni Received Received
  P1-092 A rare case of pseudoisodicentric X chromosome in a patient with primary amenorrhoea Saskia Schipper Received Received
  P3-092 Case of family neonatal diabetes with KCNJ11 gene mutation: dynamics monitoring Svitlana Chumak Received Received
  P2-093 The growth hormone treatment and carbohydrate metabolism in children born small for gestational age. Dominika Labochka Received Received
  P1-093 Persisting Embryonal Infundibular Recess in a patient with Morning Glory Syndrome and multiple pituitary deficiencies ADALGISA FESTA Received Received
  P1-094 Familial occurrence of Turner syndrome in two Tunisian families imen gargouri Received Received
  P2-094 Empirical sulphonyurea in Neonatal diabetes: results from a aTertiary care centre smita ramachandran Received Received
  P3-095 Changes in the Microbiome of Pre-Type 1 Diabetic Children Nikolina Zhelyazkova Received Received
  P2-095 Diabetes Mellitus, Severe Acanthosis Nigricans and Short Stature: a Rare Association in Chinese Children Miaoying Zhang Received Received
  P1-095 The role of physical activity on postural stability and fitness characteristics in pediatric patients with GH deficiency Maria Cristina Maggio Received Received
  P3-096 Assessment of cardiac function in obese children and adolescents with metabolic syndrome Penio Kassari Received Received
  P2-096 Evaluation of celiac disease antibodies and 25-OH vitamin D in type 1 diabetic patients Lusine Navasardyan Received Received
  P1-096 Assessment of subjective and objective compliance to growth hormone therapy of children with growth hormone deficiency Elpis Athina Vlachopapadopoulou Received Received
  P3-097 Metabolic Syndrome in adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency imen gargouri Received Received
  P1-097 Familial Neurohypophyseal Diabetes Insipidus and 2 Novel Vasopressin Gene Mutations in 13 Italian Kindreds. GIUSEPPA PATTI Received Received
  P2-097 Does commencing on an insulin pump improve glycaemic control in paediatric patients? Nuthana Prathivadi Bhayankaram Received Received
  P3-098 High allostatic load in children with excess of weight Valeria Calcaterra Received Received
  P1-098 Final height in oncological growth hormone deficient (GHD) children after growth hormone (GH) therapy Giulia Rodari Received Received
  P2-098 Prevalence of Neonatal Macrosomia (NM) and Its Relation to Hypoglycaemia (NH) in Normoglycemic Versus Dysglycemic Pregnant Women. Ashraf Soliman Received Received
  P1-099 Eating Behavior and Oxytocin in Childhood-onset Craniopharyngioma Patients: An Exploratory Study Hermann L. Muller Received Received
  P2-099 A Case of Neonatal Diabetes Due to Newly Defined Mutation in the GLIS 3 Gene Yilmaz Kor Received Received
  P3-099 Influence of eating habits, sleep patterns and physical activity on anthropometric variables and body composition in children with obesity. Leandro Soriano-Guillén Received Received
  P2-100 Hypertriglyceridemia as a complication of severe diabetic ketoacidosis in newly diagnosed diabetes - a case report. Matylda Hennig Received Received
  P1-100 RNPC3 mutations associate prolactin deficiency and ovarian insufficiency, expanding the phenotype beyond isolated growth hormone deficiency type V (MIM618860) Gabriel Á. Martos-Moreno Received Received
  P3-100 An infant with severe hypertriglyceridemia: Acute and long-term management in the paediatric population Sarah WY Poon Received Received
  P3-101 BigO: The use of new technologies for the management of childhood obesity A clinical pilot study Penio Kassari Received Received
  P2-101 Evaluation of the Effect of Knowledge Levels of Adolescents Diagnosed with Type 1 Diabetes Melllitus on Hba1c and Life Quality Score Keskin Meliksah Received Received
  P1-101 Identification of novel mutations in FGFR1 and functional characteristics in patients with isolated gonadotropin-releasing hormone deficiency Yena Lee Received Received
  P1-102 Clinical Presentation, Management, and the Outcomes of Pituitary Adenomas in children aashish sethi Received Received
  P2-102 FLASH GLUCOSE MONITORING SYSTEM VERSUS BLOOD SUGAR TEST STRIPS: COST COMPARISON AND SATISFACTION DURING A YEAR IN A NORTHERN SPAIN REGION MARIA LAURA BERTHOLT ZUBER Received Received
  P3-102 Obesity and Insulin Resistance: Differences between pubertal and prepubertal children Eirini Dikaiakou Received Received
  P1-103 A case of panhipopituitarism with SOX3 gene deletion Esra Dger Received Received
  P3-103 Relationship between 25-hydroxyvitamin D with adiposity assessed by body mass index, serum glucose and lipids levels in Korea : a cross-sectional analysis Kye Shik Shim Received Received
  P2-103 Evaluation of the association of glutamic acid decarboxylase antibody and limbic encephalitis in children with type 1 diabetes mellitus Esra Dger Received Received
  P2-104 Insulin pump therapy implementation in Uzbekistan Khilola Hanmehmet Received Received
  P1-104 Interesting Genotype-Phenotype Differences in Siblings with Familial Hypopituitarism and Pituitary Hypoplasia Emma Thorley Received Received
  P3-104 Treating Paediatric Morbid Obesity using the Multidisciplinary Intensive Inpatient Approach Ruma Deshpande Received Received
  P2-105 Cardiopulmonary exercise testing, body composition and metabolic status after allogeneic hematopoetic stem cell transplantation in childhood Kathleen De Waele Received Received
  P1-105 Familial Central Precocious Puberty Caused by a Novel MKRN3 Mutation Osnat Admoni Received Received
  P3-106 PHENOTYPIC AND GENOTYPIC PROPERTIES OF CHILDREN WITH SUSPICION OF MONOGENIC OBESITY Hayrullah Manyas Received Received
  P1-106 Management and treatment outcome of craniopharyngiomas in young children before 4 years of age in Italy: multicentre collection of 16 cases Federico Baronio Received Received
  P2-106 School-age children awareness of seriousness of obesity problem, health-related outcomes and effectiveness of self-control preventive strategies Tetyana Chaychenko Received Received
  P2-107 Childhood Obesity and Iron Metabolism Julia Galhardo Received Received
  P3-107 Relation of serum 25 hydroxy-vitamin levels D3 with body-mass index in pediatric patients paula sol ventura wichner Received Received
  P3-108 VITAMIN B12 LEVELS IN CHILDREN AFTER METFORMIN TREATMENT Kostova Yordanova Received Received
  P2-108 Effectiveness of Multidisciplinary Outpatient Approach in the Management of Paediatric Obesity Ruma Deshpande Received Received
  P2-109 Metabolic syndrome in children and adolescents who survived after childhood cancer. Anna Gavrilova Received Received
  P1-109 A NCOA5 gene variant in a pedigree with maternally inherited precocious puberty Magdalena Avbelj Stefanija Received Received
  P3-109 Follow-up evaluation of clinical markers and inflammatory, biochemical and hormonal profiles in children with bodyweight problems Ioana Taranu Received Received
  P2-110 Pubertal milestones and related hormonal changes among children with obesity Robert Stein Received Received
  P1-110 Novel references for ultrasound estimated testicular volumes and pubic hair in 6-16 year-old Norwegian boys Ninnie Oehme Received Received
  P3-110 Gastroduodenopathies in obese young people Olena Tolstikova Received Received
  P1-111 PROKR2 in in girls with idiopathic central precocious puberty Anna Grandone Received Received
  P3-111 Seven Methods of indicating childhood Metabolic Syndrome shahin koohmanaee Received Received
  P2-112 Identification of a novel heterozygous missense mutation in low-density lipoprotein receptor gene (LDLR) p.(Met652Thr) in an Emirati family with familial hypercholesterolaemia (FH), observed genotype-phenotype correlations and pharmacotherapeutic approach Lara Al-Olabi Received Received
  P3-113 SEVERE HYPERNATREMIA REVEALING A ROHHAD-NET SYNDROME. YASMINE OUAREZKI Received Received
  P2-113 Prevalence and correlation of Non alcoholic fatty liver disease (NAFLD) with serum Alanine Aminotransferase (ALT) levels in obese Indian children Vasundhara Chugh Received Received
  P1-114 Obesity in boys is not associated with delayed pubertal onset Alexander Busch Received Received
  P3-114 RARE CASE OF ACQUIRED GENERALIZED LIPODYSTROPHY IN A 14-YEAR OLD PATIENT Dumitrescu Cristina Patricia Received Received
  P3-115 Gender-based differences in the clustering of metabolic syndrome factors in children and adolescents. Valeria Calcaterra Received Received
  P1-115 Mutation screening of the Sonic Hedgehog signaling-related genes in 120 Japanese patients with congenital hypopituitarism Masaki Takagi Received Received
  P2-115 The prevalence of severe obesity and related comorbidities has increased during the last decade among children and adolescents referred for evaluation at the obesity clinic. shlomit shalitin Received Received
  P1-116 How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty tarik kirkgoz Received Received
  P3-116 Fat mass index and fat-free mass index percentiles in healthy Spanish adolescents. Teodoro Durá-Travé Received Received
  P2-116 Nonalcoholic Fatty Liver Disease in Pediatric Obese Patients giorgiana brad Received Received
  P2-117 Trends in childhood obesity, underweight and short stature among urban school children in Romania Raluca-Monica Pop Received Received
  P1-117 The Role of Rat Hypothalamus Kisspeptin, Neurokinin and their respective Receptors in the Prolactin-Infertility Interaction Bertan Yilmaz Received Received
  P3-117 Comparison of Different Criteria for the Definition of Insulin Resistance and Its Relation with Metabolic Risk in Overweight and Obese Adolescents Yujung Choi Received Received
  P3-118 Somatostatine Analogue in Hypothalamic Obesity Belma Haliloglu Received Received
  P2-118 Impact of a comprehensive program, on prevalence of childhood obesity in Andalusia, Spain. María Rocío Hernández-Soto Received Received
  P1-118 Whole Exome Sequencing (WES) reveals oligogenic gene mutations in a case of Combined Pituitary Hormone Deficiency (CPHD). AMALIA SERTEDAKI Received Received
  P3-119 PHYSICAL ACTIVITY, FOOD AND METABOLIC RISK IN CHILDREN AND ADOLESCENTS Carmela de Lamas Received Received
  P2-119 Evaluation of Fetuin-A level and related factors in obese adolescents Glin Karacan Kucukali Received Received
  P1-119 Menarche and its relation to the pubertal growth spurt Jenni Gardstedt Received Received
  P2-120 Prevalence of Obesity among Infants Presenting with Intussusception Omar Magdy Omar Received Received
  P1-120 ROLE OF PRIMING IN PERI-PUBERTAL GROWTH DELAYS: PRELIMINARY RESULTS OF A LARGE MULTICENTER STUDY Elena Galazzi Received Received
  P3-120 Toward a simple marker of hepato-visceral adiposity and insulin resistance:the Z-score change from weight-at-birth to BMI-in-childhood Rita Malpique Received Received
  P3-121 Associations between lipid parameters and insulin resistance in obese adolescents Tetyana Chaychenko Received Received
  P2-121 A non-invasive model for detection of the metabolic syndrome in children and adolescents Junfen Fu Received Received
  P1-121 Lower urinary tract dysfunction and infection in girls with disorders of sex development and urogenital sinus Alexander Anikiev Received Received
  P3-122 THE CHARACTERISTIC OF THYROID STATUS IN OVERWEIGHT AND OBESE YOUNG PEOPLE WITH INSULIN RESISTANCE Olena Tolstikova Received Received
  P2-122 Insulin-like growth factor-1 and binding protein-3 in children with metabolic syndrome yoonji Lee Received Received
  P2-123 Overweight, obesity and hypertension among adolescents the impact of immigration and a acculturation Orit Hamiel Received Received
  P1-123 Does the internet provide accurate and valid health information regarding disorders of sex development? Toby Candler Received Received
  P3-123 Validity of non-high-density lipoprotein cholesterol for detecting dyslipidemia among Korean adolescents Hyo-Kyoung Nam Received Received
  P1-124 A human model showing the ability of testis XX cells to masculinise into Sertoli cells and success of microTESE surgery in paediatric azoospermia Gabby Atlas Received Received
  P3-124 EARLY ONSET MONOGENIC OBESITY: TWO CASES WITH HOMOZYGOUS MUTATION IN LEPR GENE Ozlem Nalbantoglu Received Received
  P1-125 A Health-Related Quality of Life Tool for Parents of Young Children With Disorders of Sex Development Salma Ali Received Received
  P3-125 Fasting C-Peptide: A useful tool for diagnosis of Type II Diabetes Mellitus in overweight / obese adolescents living in a poor resources setting. Adele Bodieu Kenmegne Spse Chetcha Received Received
  P2-125 Clinical features and genetic analysis of childhood dyslipidemia Chao chun Zou Received Received
  P1-126 Longitudinal Changes In External Masculinisation Scores In Boys With XY Disorder Of Sex Development (DSD) Malika Alimussina Received Received
  P2-126 TRACKING BODY MASS INDEX AND FAT MASS PERCENTAGE FROM INFANCY INTO CHILDHOOD Inge van Beijsterveldt Received Received
  P3-126 Metabolic risk assessment in obese children using Hypertriglyceridemic waist (HTGW) phenotype. Can it be a useful screening marker? Eirini Dikaiakou Received Received
  P2-127 The bilirubin/triglycerides ratio predicts changes over time in glycated hemoglobin in prepubertal healthy children Elsa Puerto-Carranza Received Received
  P1-127 Mutations in CBX2 associated with gonadal anomalies in 46,XY and 46,XX individuals Ken McElreavey Received Received
  P3-128 Lipid and glucose profiles in obese Algerian children and adolescents Soraya Kerkouche Received Received
  P1-128 The novel founder homozygous V225M mutation in the 17HSDB3 gene causes aberrant splicing and severe XY-DSD Floris Levy-Khademi Received Received
  P2-128 Is one year of diet and physical activity program for obese children enough to revert the metabolic disorders? Beatriz Garcia Cuartero Received Received
  P1-129 Molecular diagnosis of patients with 46,XY differences in sex development in a single tertiary center. Natalia Perez Garrido Received Received
  P2-129 CHARACTERIZATION OF ADHERENCE TO FOLLOW-UP AND THERAPEUTICAL OUTCOMES IN A LARGE COHORT OF 1300 PATIENTS WITH OBESITY VISITED IN A SPECIALIZED TERTIATY CARE CENTER Gabriel Á. Martos-Moreno Received Received
  P3-129 The effect of anthropometric indices at birth on obesity characteristics in school-age children Dmitriy Latyshev Received Received
  P3-130 Acanthosis nigricans as a presentation of severe insulin resistance in obese children. Maria Krajewska Received Received
  P2-130 SEVERE OBESITY MUCH MORE THAN AN UNHEALTHY LIFESTYLE Joana Matias Received Received
  P2-131 Serum 25-Hydroxyvitamin D Levels and Insulin Sensitivity Across Pubertal Stages in Obese Children Somboon Wankanit Received Received
  P1-131 Is there the relationship between anxiety and depression level and clinical presentation of polycystic ovary syndrome in adolescent girls? Agnieszka Zachurzok Received Received
  P3-132 Recurrent apnea in a boy suffering from congenital hyperinsulinism in the course of diazoxide treatment. J&281;drzej Nowaczyk Received Received
  P2-132 ASSOCIATION BETWEEN TSH AND METABOLIC SYNDROME IN OBESE CHILDREN AND ADOLESCENTS Chiara Guzzetti Received Received
  P1-132 What is the recurrence rate of benign ovarian tumors in childhood? Ovarian Benign organic Tumors (OBT) are a rare pathology in childhood that require conservative surgery with an unknown risk of recurrence. Audrey Cartault Received Received
  P3-133 RELATIONS OF O2 SUPPLEMENTATION TO BLOOD SERUM INSULIN-LIKE GROWTH FACTOR-I IN THE NOT-LIFE-THREATENED HUMAN NEWBORN; ROLE OF ORAL-ENTERAL CALORIC INTAKE BEYOND AXILLARY TEMPERATURE. Cesare Terzi Received Received
  P2-133 Primary hyperlipidemia in children: experience of 11 years from a referral center in Vietnam Mai Do Received Received
  P2-134 TUMOR NECROSIS FACTOR ALPHA IN METABOLIC SYNDROME DEVELOPMENT IN CHILDREN Iwona Be&324;-Skowronek Received Received
  P3-134 Persistant Hypoglycemia in Children: Hyperinsulinemia gl direk Received Received
  P1-135 Combining clinical and genetic approaches in diagnosing a large Brazilian cohort of patients with 46,XY Differences of Sex Development (DSD) NATHALIA GOMES Received Received
  P2-135 First Familial Occurrence of Prader-Willi Syndrome in China: Two Cases and Family Studies Yunqi Chao Received Received
  P2-136 Insulin resistance and impaired glucose tolerance in overweight/obese adolescents attending an obesity clinic in Belgium Renate Zeevaert Received Received
  P1-136 Serum estradiol is associated with inhibin B in healthy 1-6 years old girls. Niels Birkebaek Received Received
  P1-137 Brain MRI Findings in Girls with Central Precocious Puberty in Taiwan: one medical center experience FU-SUNG LO Received Received
  P2-137 Clinical characteristics and response to growth hormone treatment in patients with Prader-Willi Syndrome Aydilek ak&305;r Received Received
  P3-137 Case report: A neonate with prolonged hypoglycemia Adele Bodieu Kenmegne Spse Chetcha Received Received
  P3-138 Factors affecting Growth Response to Growth Hormone ( GH) therapy in children with short stature and normal GH and IGF-I secretion and no bone age delay. Ahmed Elawwa Received Received
  P1-138 Changes in body mass index in boys with central precocious puberty during and after gonadotropin-releasing hormone agonist treatment Chang Dae Kum Received Received
  P1-139 Gonadal function of female patients with Noonan syndrome Sophie Moniez Received Received
  P2-139 The prevalence of elevated blood pressure and hypertension in Korean adolescents, based on the guidelines of Endocrine Society and American Academy of Pediatrics In-Hyuk Chung Received Received
  P3-139 Responses to growth hormone (GH) therapy in children with short stature with normal GH secretion and slow growth velocity. Ashraf Soliman Received Received
  P1-140 Methylation status of X inactivation-escape genes in controls and females with X chromosome rearrangements Sayaka Kawashima Received Received
  P3-140 Assessment of body composition of Children with short stature on growth hormone therapy and its relation to serum IGF-1 Amany El-hawary Received Received
  P2-140 PEDOBESITY: Development of Intelligent Multi-level Information Systems and Specialized Artificial Intelligence Algorithms for Personalized Management of Obesity in Childhood and Adolescence Penio Kassari Received Received
  P2-141 Metabolic syndrome risk assessment in Indian children and adolescents Vasundhara Chugh Received Received
  P3-141 TREATMENT OUTCOME OF GROWTH HORMONE IN TURNER SYNDROME CHILDREN Bui Phuong Thao Received Received
  P1-141 Diagnostic Value of Anti-Mullerian Hormone Level in Adolescent Females with Polycystic Ovary Syndrome Shereen Abdelghaffar Received Received
  P2-142 Vitamin D status in obese children and its relationship with leptin and adiponectin Mona Nourbakhsh Received Received
  P1-142 Disorders of sex development (DSD): Inconsistencies between clinical features and peripheral blood cultured karyotypes Nursen Gurtunca Received Received
  P1-143 BIOTINE INTERFERENCE IN A PATIENT WITH NON-CLINIC HIGH THYROID HORMONE LEVELS Hayrullah Manyas Received Received
  P2-143 Two Siblings with Tyrosinaemia Type 1 and Transient Hyperinsulinaemic Hypoglycaemia Ellada Sotiridou Received Received
  P3-144 A case of paediatric GH-secreting pituitary adenoma apoplexy Dario Gallo Received Received
  P2-144 Glucagon therapy in preterm infants with hyperinsulinemic hypoglycaemia Roschan Salimi Dafsari Received Received
  P2-145 NEONATAL HYPO-KETOTIC HYPOGLYCEMIA SECONDARY TO TRANSIENT HYPERINSULINISM. DIAZOXIDE RESPONSIVENESS AND EXPERIENCE WITH FASTING TEST AFTER TREATMENT WITHDRAWAL Luis Salamanca Received Received
  P1-145 The investigation of genetic etiology in familial cases with congenital hypothyroidism Feyza Darendeliler Received Received
  P3-146 GROWTH HORMONE DEFICIENCY AFTER RADIATION THERAPY FOR BRAIN TUMOR HOW TO MANAGE ? OUIDAD BAZ Received Received
  P2-146 Severe Neonatal Hyperparathyroidism Due to a Novel Homozygous Mutation of the Calcium-Sensing Receptor (CaSR) amir hacohen solovitz Received Received
  P1-146 Is there any correlation between thyroid function test on first day of admission in critically ill children and disease severity or outcome? fatemeh sayarifard Received Received
  P1-147 Intrathyroidal ectopia of thymus in children: frequency, ultrasound, evolution. Goar Okminyan Received Received
  P2-147 A rare cause of pediatric hypoglycemia in a boy: a malignat insulinoma Mariella Valenzise Received Received
  P1-148 Activating mutation M453V in receptor TSHR as a cause familial hyperthyroidism Beata Sawicka Received Received
  P1-149 Central hypothyreoidism with pituitary enlargement and no gene alterations Zoran Gucev Received Received
  P2-149 Clinical and genetic characteristics of patients with hyperinsulinaemic hypoglycaemia diagnosed and treated at a tertiary endocrine center, a part of the ENDO-ERN Sonya Galcheva Received Received
  P2-150 RELATIONS OF O2 SUPPLEMENTATION TO BLOOD SERUM INSULIN-LIKE GROWTH FACTOR-II / INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-3 RATIOS IN THE NOT-LIFE-THREATENED HUMAN NEWBORN; ROLE OF ORAL-ENTERAL CALORIC INTAKE BEYOND AXILLARY TEMPERATURE. Cesare Terzi Received Received
  P3-150 Features of somatropin replacement therapy in a patient with Floating Harbor Syndrome Olga Berseneva Received Received
  P2-151 Refractory Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Imprinting Centre 1 Gain of Methylation: Severity Discordant to Genotype. Louise Conwell Received Received
  P1-152 THYROID FUNCTION FOLLOWING HEMITHYROIDECTOMY IN A PEDIATRIC COHORT Patricia Papendieck Received Received
  P2-152 Congenital Hyperinsulinism due to Compound Heterozygous mutations in ABCC8 fully responsive to Diazoxide therapy. Tashunka Taylor-Miller Received Received
  P3-152 Linear Growth of infants with neonatal and early infantile meningitis Ashraf Soliman Received Received
  P2-153 Criteria for first-year growth response to growth hormone treatment in prepubertal children with growth hormone deficiency: do they predict poor final height? Saartje Straetemans Received Received
  P1-153 Homozygous c.2422delT hTPO mutation in three patients with congenital hypothyroidism followed over 20 years Kalina Mihova Received Received
  P3-153 Prevalence of Thyroid Dysfunction and Associated Autoimmune Disorders in Young Children with Down Syndrome (DS); A Cohort Study. Nada Alaaraj Received Received
  P1-154 Association of Hashimotos Thyroiditis with Antistreptolysin O titer. Antonis Voutetakis Received Received
  P2-154 Determinants of the peak GH response of the glucagon stimulation test in slowly growing children. Jean De Schepper Received Received
  P3-155 Turners Syndrome - clinical presentation, genetics, investigation and management: a 10-year review Hassan Elechi Received Received
  P1-156 PROSPECTIVE, OPEN-LABEL, LONG-TERM FOLLOW-UP OF NEONATES AND YOUNG CHILDREN WITH ADRENAL INSUFFICIENCY TREATED WITH HYDROCORTISONE GRANULES Uta Neumann Received Received
  P3-156 Growth Status of children and adolescent born Full Term Small-for-Gestational-Age in Korea: Data from the KNHANES-V (2010-2011) Jung Sub Lim Received Received
  P2-156 Growth hormone monotherapy versus Combined GH and LHRH analog in 2 sisters with short stature, early pubertal development, and advanced bone age (BA). Sohair Elsiddig Received Received
  P3-157 Bardet-Biedl syndrome: a case series Ana Raquel Mendes Received Received
  P2-157 Long-term follow-up of three patients with isolated growth hormone deficiency type IA withsustained growth response to rhGH. Svetlana Babinskaya Received Received
  P1-157 Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry Uta Neumann Received Received
  P3-158 A novelvariant of KAT6B caused Say-Barber-Biesecker-Young-Simpson syndrome Ying Weng Received Received
  P2-158 Clinical and genetic characteristics of eleven Korean patients with hypochondroplasia and outcomes of growth hormone therapy. Min-Sun Kim Received Received
  P2-159 Growth hormone treatment adherence in Latin American patients: 2-year real world data from the easypod connect eHealth platform Joanna Foley Received Received
  P1-159 Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency Zehra Yavas Abali Received Received
  P3-159 THREE CASES WITH FAMILIAL SHORT STATURE: LERI-WEILL SYNDROME Hayrullah Manyas Received Received
  P1-160 Serum fetuin-A and insulin levels in classic congenital adrenal hyperplasia Erdal Kurnaz Received Received
  P2-160 METABOLIC OUTCOME IN ADOLESCENTS WITH GROWTH HORMONE DEFICIENCY DURING TRANSITION PHASE Nicola Improda Received Received
  P3-160 Thyroid Dysfunction in the First Year of Life in Infants with Down syndrome: Linear Growth Over 4 Years. Nada Alaaraj Received Received
  P3-161 The Effect of Thyroxine Treatment on Linear Growth and Weight Gain in Infants and Children with Down Syndrome (DS) and High TSH versus Children with DS and normal thyroid function: A controlled study Ashraf Soliman Received Received
  P1-161 Perioperative control of blood pressure in a child with paraganglioma using Esmolol AMIR BABIKER Received Received
  P2-161 The Influence of pituitary MRI findings on clinical presentation and growth in GH-Treated Children with Congenital Hypopituitarism Adel DJERMANE Received Received
  P1-162 Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3-hydroxysteroid dehydrogenase 2 deficiency TULAY GURAN Received Received
  P2-162 Metabolic effects of growth hormone treatment in short prepubertal children: a double-blinded randomized clinical trial Anders Tidblad Received Received
  P3-163 Endocrinological evaluation of male patient with Floating-Harbor syndrome case report Maja Oko&324;ska Received Received
  P2-163 Growth response in short preterm- born children small for gestational age in first year of growth hormone treatment Maria Korpal-Szczyrska Received Received
  P1-164 The urinary steroid signature of premature adrenarche Marco Janner Received Received
  P3-164 Longitudinal evaluation of audiological pattern in Turner syndrome Tommaso Aversa Received Received
  P2-164 BRAIN MAGNETIC RESONANCE IMAGING IN CHILDREN WITH ISOLATED GROWTH HORMONE DEFICIENCY Pamela Yesquen Received Received
  P3-165 Final adult height in a patient with Turner syndrome 46, X, i(Xq) treated with growth hormone for 10 years compared to her normal dizygotic twin sister and mid-parental height. noor Hamed Received Received
  P2-165 The clinical significance of post-sleep growth hormone levels in the diagnosis of growth hormone deficiency Chaeri Yoo Received Received
  P1-165 How the level of antibodies against 21-hydroxylase changes with time in patients with Addisons disease Leila Sozaeva Received Received
  P3-166 Growth hormone treatment and puberty in patient with Pallister-Hall syndrome. Elena Pisareva Received Received
  P1-166 Cortisol levels in glucagon stimulation tests in children evaluating for short stature: clinical and laboratorial correlations Athanasios Christoforidis Received Received
  P2-166 Prediction of the first-year response to growth hormone treatment in prepubertal Korean children with idiopathic growth hormone deficiency: analysis of data from the LG Growth Study database won kyoung cho Received Received
  P2-167 Adherence and long-term outcomes of therapy in pediatric subjects in Argentina using easypod electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod Connect Observational Study (ECOS) Cinthia Chareca Received Received
  P1-167 Development Of An International Benchmark For Sick Day Episodes As A Core Clinical Outcome In People With Congenital Adrenal Hyperplasia Salma Ali Received Received
  P3-167 Bloom Syndrome in 7-year-old girl diagnosed with short stature. Hanna Borysewicz-Sa&324;czyk Received Received
  P3-168 Efficacy of growth hormone treatment in a patient with chronic granulomatous disease, who developed acute myeloid leukemia after bone marrow transplantation. Gianluca Tornese Received Received
  P2-168 Adherence and long-term outcomes of therapy in pediatric subjects in Slovakia using easypod electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod Connect Observational Study (ECOS) Ludmila Kotálová, Svetlana Bieliková, Marcela Balosakova Received Received
  P1-168 Genotype-phenotype characteristics in four families of type 2 collagenopathy in our hospital Kenichi Yamamoto Received Received
  P3-169 Schaaf-Yang syndrome:Three cases report of MAGEL2 variation and literature review Xuefei Chen Received Received
  P2-170 Growth hormone therapy in patients with SGA short stature improves body composition by increasing muscle mass and bone mineral density rather than decreasing fat mass. Takatoshi Maeyama Received Received
  P3-170 Reevaluation of congenital growth hormone deficiency in adulthood imen gargouri Received Received
  P1-170 Efficacy and safety of denosumab treatment in a prepubertal patient with cherubism Haruka Kawamura Received Received
  P1-171 Bone health in adolescents and young adults after allogeneic hematopoetic stem cell transplantation in childhood: a single center cross-sectional study. Kathleen De Waele Received Received
  P2-171 Final height in GH-deficient paediatric patients: a nationwide experience Stefano Zucchini Received Received
  P3-172 Pure gonadal dysgenesis with partial testicular development associated with Turner syndrome with SRY Kyung Hee Yi Received Received
  P2-172 DIFFERENCES OF EFFICIENCY OF TREATMENT OF ISOLATED GROWTH HORMONE DEFICIENCY AND PANHYPOPITUITARISM IN CHILDREN IN REAL CLINICAL PRACTICE Ekaterina Rudkova Received Received
  P3-173 A case of WiedemannSteiner syndrome with central precocious puberty Kohei Aoyama Received Received
  P1-173 Cutoff value for 25 Hydroxy-vitamin D which leading to symptomatic vitamin D deficiency in children is 15 ng/mL in a chemiluminescent immunoassay Yasuko Ogiwara Received Received
  P2-173 Implementation of a growth disorders related twinning program in pediatric endocrinology is it necessary and feasible? Irina Halvadzhiyan Received Received
  P1-174 The Optimal Dosage of Vitamin D Supplement for Vitamin D deficiency in Korean Children and Adolescents Seung Yang Received Received
  P2-174 Empirical change of practice in treatment of growth hormone deficient patients in order to improve 1st year height outcome Kamelia Rankova Received Received
  P3-174 Population prevalence of Downs syndrome and cardiac complications in South Korea: Based on National Health Insurance Service (NHIS) NA YEONG LEE Received Received
  P2-175 The impact of Growth hormone treatment in patients with Noonan syndrome and growth hormone deficiency Hae Sang Lee Received Received
  P1-175 Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees Sare Betul Kaygusuz Received Received
  P3-175 McCune Albright Syndrome: Two cases with different clinical courses. Agim Gjikopulli Received Received
  P1-176 Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA Sare Betul Kaygusuz Received Received
  P2-176 Efficacy and safety of growth hormone (GH) in the treatment of children with hypochondroplasia (HCH): comparison with a historical cohort of untreated children with HCH graziella pinto Received Received
  P1-177 Severe Hypocalcaemia in Propionic Acidaemia caused by Parathyroid Hormone Resistance and treated with Alfacalcidol. Jessica Sandy Received Received
  P2-177 Five Novel Variants of KMT2D/KDM6A Found in Seven Chinese Patients with Kabuki syndrome and a literature review of 39 patients reported in China Ruimin Chen Received Received
  P2-178 Adult height of patients enrolled in PATRO Children, an ongoing observational study of the long-term safety and effectiveness of Omnitrope Tony Reardon Received Received
  P1-178 The Efficacy and Safety of Predictive Low Glucose Suspend Feature in Decreasing Hypoglycemia in Children with Type 1 Diabetes Mellitus: a systematic review and meta-analysis Ahlam Alotaibi Received Received
  P3-178 Long-term effect of growth hormone treatment on the onset and progression of scoliosis in children with Prader-Willi Syndrome. Lionne Grootjen Received Received
  P2-179 UNUSUAL CASE OF PATIENT WITH KLINEFELTER SYNDROME WITH SHOX DELETION BORN TO THE MOTHER WITH LERI-WEILL DYSCHONDROSTEOSIS Nevena Krnic Received Received
  P1-179 Longitudinal metabolic control after initiation of insulin pump in 5,040 pediatric type-1-diabetes subjects heterogeneous HbA1c trajectories over three years from the DPV registry Nicole Prinz Received Received
  P3-179 Clinical and molecular characteristics of pediatric patients with multiple endocrine neoplasia (MEN) Yena Lee Received Received
  P3-180 APECED Syndrome in Childhood: Rare Clinical Presentations to Keep in Mind Semra etinkaya Received Received
  P2-180 Sudden death in an infant attributed to arrhythmia associated with Beckwith-Wiedemann Syndrome due to hypomethylation of imprinting control region 2 on chromosome 11p15.5 aashish sethi Received Received
  P1-180 Efficacy and Safety of Insulin Degludec as a basal insulin in adolescents with Type 1 Diabetes during Ramadan fasting: A single center observational study with freestyle libre flash glucose monitoring system Nancy Elbarbary Received Received
  P3-181 Phenotype and clinical course in three individuals with Multiple Endocrine Neoplasia Type 2A due to a RET gene mutation. Evangelia Panou Received Received
  P1-181 A case of prohormone convertase deficiency diagnosed with type 2 diabetes mellitus Senay Savas-Erdeve Received Received
  P3-182 Two Siblings Case with Diagnosis of Autoimmune Polyglandular Syndrome Type 1 Hayrullah Manyas Received Received
  P1-182 The influence of excess iron on pancreatic beta cells Lina ZHANG Received Received
  P2-182 Auditory phenotypes and dynamics of hearing thresholds in 246 Turner syndrome females Tommaso Aversa Received Received
  P3-183 High demand for collaborative work between paediatric endocrinologists in Arab countries Hussain Alsaffar Received Received
  P2-183 The Prevalence of Celiac Disease (CD) in Children with Type 1 Diabetes Mellitus (T1D); Does CD adversely affect linear growth in these children? fawziya Alyafei Received Received
  P1-183 Study on the mechanism of metformin in improving PGRN-induced insulin resistance of 3T3-L1 cell Siqi Huang Received Received
  P1-184 A case with monogenic diabetes caused by RFX6 mutation in a 14-year-old-girl Jeesuk Yu Received Received
  P2-184 Effect of Gonadotropin-Releasing Hormone Agonists on Auxological Outcomes of Korean Boys with Central Precocious puberty and Early Puberty Hae Sang Lee Received Received
  P3-184 Eosinophilic Ascites: a rare complication of autoimmune polyendocrinopathy Zacharoula Karabouta Received Received
  P1-185 Endothelial and heart dysfunction in children and adolescents with type 1 diabetes. Barbara Predieri Received Received
  P3-185 Final height and endocrine complications in patients with -thalassemia intermedia: (TI) Our experience in non-transfused versus infrequently transfused patients and correlations with liver iron content Ashraf Soliman Received Received
  P3-186 Variable expressivity in three generation from a Colombian family with multiple endocrine neoplasia with mutation c.482GA (p.Gly161Asp) in the gene MEN1 not described in Colombia. Liliana Mejia de Beldjenna Received Received
  P2-186 Clinical features in a patient with Turner syndrome and pericentric inversion of chromosome 9 Mariella Valenzise Received Received
  P3-187 Difficulties in hypothyroidism and diabetes treatment in patient with GATA6 gene mutation case report. Maja Oko&324;ska Received Received
  P2-187 Less Ready for Adulthood? Turner syndrome has an impact on transition readiness Caroline Culen Received Received
  P2-188 Clinical and molecular genetic characterizations of five patients harboringmutations in the GNAS gene: a case series and literature review Qun Li Received Received
  P1-188 A novel mutation in the Pancreatic duodenal homeobox-1(PDX-1) gene in a Palestinian family resulting in Neonatal Diabetes associated with congenital adrenal hyperplasia Abdulsalam Abu-Libdeh Received Received
  P3-188 Endocrinopathies and linear growth in adolescents with -thalassemia intermedia in Relation to liver iron content. Ashraf Soliman Received Received
  P1-189 A Novel SLC2A2 mutation implicated in Fanconi Bickel syndrome and dysglycemia Sanaa Sharari Received Received
  P3-189 Bardet-Biedl syndrome: Not only what but also how matters? Narjess Boutalbi Received Received
  P2-189 Anophthalmia, micrognathia, combined pituitary hormone deficiency, severe growth retardation and liver dysfunction induced levothyroxine sodium powder in a boy with microdeletion of 14q22q23 Satomi Koyama Received Received
  P3-190 STRUCTURAL PITUITARY ABNORMALITY AND DYSFUNCTION ASSOCIATED WITH CHARGE SYNDROME Feneli Karachaliou Received Received
  P2-190 Growth Hormone Therapy in patients with Noonan Syndrome Louise Apperley Received Received
  P1-191 Effect of Probiotics intake on obese children Ruimin Chen Received Received
  P3-191 Hormone-secreting pituitary adenomas in children and adolescents Natallia Akulevich Received Received
  P3-192 ROHHAD SYNDROME: REPORT OF 2 RARE CASES FROM CRETE-GREECE PINELOPI SMYRNAKI Received Received
  P1-192 Changes in objectively measured sleep quality after an integral intervention in patients with abdominal obesity Cristina Azcona Received Received
  P2-192 SHOX-HAPLOINSUFFICIENCY INTRA-FAMILIAL PHENOTIPIC VARIABILITY AND THE IMPACT ON FINAL HEIGHT: REPORT OF A PEDIGREE Maria Cristina Maggio Received Received
  P1-193 Circulating Insulin-like Growth Factor-I independently predicts blood pressure in apparently healthy children Abel López-Bermejo Received Received
  P2-193 Linear Growth of Children with Celiac Disease (CD) after the first two years on a Gluten-free Diet (GFD); A Controlled Study Ashraf Soliman Received Received
  P3-194 Coincidental Central Precocious Puberty and Wilms Tumor ramona nicolescu Received Received
  P2-194 Growth hormone treatment adherence in patients from an emerging economy country: 1-year real-world data from the easypod connect eHealth platform Paula Barquero Received Received
  P2-195 The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation Ayse Pinar OZTURK Received Received
  P1-195 Serum leptin, adiponectin and insulin-like growth factor I during infancy were associated with markers of metabolic syndrome at six years of age Jovanna Dahlgren Received Received
  P2-196 KLINEFELTER SYNDROME ASSOCIATED WITH SHORT STATURE DUE TO IATROGENIC CUSHING RENATA PINTO Received Received
  P3-196 Precocious pseudo-puberty presenting with bilateral ovarian involvement and progressing to juvenile granulosa cell tumor in a 2-year-old girl. hager barakizou Received Received
  P3-197 Central precocious puberty in a boy with Prader-Willi syndromeduring growth hormone replacement therapy WEI LU Received Received
  P1-197 You are what you eat: preliminary evidence of associations between dietary habits and oral microbiota composition in early childhood Melanie Henderson Received Received
  P1-198 Correlation of serum chemerin concentrations with obesity/metabolic syndrome characteristics in pre-adolescents and adolescents FLORA BACOPOULOU Received Received
  P2-198 Evaluation of Diagnosis, Follow-up and Treatment Results of Growth Hormone in Rare Diseases; 10 Year Single Center Experience zehra Aycan Received Received
  P3-198 A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation Ayhan Abac&305; Received Received
  P3-199 Prolactinomas in a Pediatric Population. liliana Mejia de Beldjenna Received Received
  P1-199 Non-alcoholic fatty liver youth with obesity Marina Ybarra Received Received
  P3-200 Extreme Short Stature and Neurological Impairment in a 17-Year-Old Male with Untreated Combined Pituitary Hormone Deficiency Due to POU1F1 Mutation Hussein Majdoub Received Received
  P2-200 Endocrine Features of Schaaf-Yang syndrome. Case report. Olena Tolstikova Received Received
  P2-201 Papillary thyroid cancer in a 17-years old girl with a late-diagnosed Turner syndrome Maria Pankratova Received Received
  P1-201 Serum Kisspeptin in Obese Children and Its Relation to Glucose Metabolism Kochakorn Sithinamsuwan Received Received
  P2-202 The applicability of the NH-Clinical scoring system on diagnosis of Iranian children with SRS Somayyeh Hashemian Received Received
  P3-202 A Case Of Syndromic Hypopituitarism Sare Betul Kaygusuz Received Received
  P1-202 Visceral adiposity index as a marker of metabolic risk in survivors of paediatric hematopoietic stem cell transplantation after chemotherapy-only conditioning Luminita-Nicoleta Cima Received Received
  P1-203 Serum nonylphenol and obesity in children and adolescents Mi Jung Park Received Received
  P3-203 Anapylaxis Secondary to Gonadotrophin Releasing Hormone Agonist used for Precocious Puberty, Two Case Reports Hala Shaikh Received Received
  P2-203 Clinical Manifestations & Molecular analysis of Thirteen Palestinian Families with Sanjad Sakatti Syndrome revealing a common deletion founder effect and another two novel mutations Abdulsalam Abu-Libdeh Received Received
  P2-204 Electromagnetic fields exposure in Adolescents: a survey in 11-14 y old Greek students Styliani Geronikolou Received Received
  P1-204 Risk factors for brain injury after transient or persistent hyperinsulinemic hypoglycemia in neonates Marcia Roeper Received Received
  P1-205 Central Hypoventilation Syndrome and Hyperinsulinaemic Hypoglycaemia Antonia Dastamani Received Received
  P3-205 Childhood craniopharyngioma: a single centre experience Dario Gallo Received Received
  P2-205 Subcutaneous ossifications in children - think about AHO Monika Flury Received Received
  P3-206 Unusual cause of hypopituitarism : A Niemann Pick Disease Mouna Mnif Feki Received Received
  P2-206 Growth outcomes in growth hormone treated indian children with celiac disease Smita Ramachandran Received Received
  P1-206 Unusual congenital hyperinsulinism case in a patient with a pathogenic GCK mutation Diliara Gubaeva Received Received
  P3-207 Precocious puberty and primary hypothyroidism in a 6 years and 10 months girl with pituitary macro adenoma and dextral ovarian cyst Ratna Artati Received Received
  P1-207 Clinical characteristics and long term follow up of 17 patients with permanent neonatal diabetes due to PTF1A distal enhancer mutations Huseyin Demirbilek Received Received
  P2-208 Autoimmune polyendocrine syndrome type I: a neuroendocrine multi-systemic disease with a variable expressivity Gerdi Tuli Received Received
  P3-209 Pituitary hyperplasia as a complication of severe hypothyroidism due to Hashimotos thyroiditis could impair pituitary function. Domenico Corica Received Received
  P1-209 Urogenital abnormalities in children conceived by assisted reproductive technologies Zinaida Zyuzikova Received Received
  P2-209 Endocrine complications of patients with hepatic type of glycogen storage disease Yena Lee Received Received
  P1-210 Subcutaneous fat necrosis of the newborn: A systematic review of the literature Stephanie Brandt Received Received
  P3-210 Homozygosity for Proopiomelanocortin (POMC) mutation in a Palestininan child Abdulsalam Abu-Libdeh Received Received
  P2-210 Autoimmune Thyroiditis and Autoimmune Hepatitis presenting at onset of Type 1 Diabetes (T1D) Alice Marchant Received Received
  P3-211 Peculiarities Of Clinical Options For Delaying Sexual Aging In Boys-Adolescents Hanna Kosovtsova Received Received
  P1-211 Characteristics of children with Kabuki syndrome and hyperinsulinemic hypoglycemia Henrike Hoermann Received Received
  P2-211 Ulnar mammary syndrome - a case report Supreetha Shetty Received Received
  P2-212 Unusual ovary formation in a girl with McCune-Albright syndrome. Nadezhda Makazan Received Received
  P3-212 Two separate pathologies (Coeliac disease and Central precocious puberty) associated with catch-up growth in the case of a child born small for gestational age (SGA). Sharon Lim Received Received
  P1-213 Determinants of final height in patients born small for gestational age treated with recombinant growth hormone. elodie adler Received Received
  P3-213 MITOCHONDRIAL ENCEPHALOMYOPATHY WITH ACIDOSIS AND STROKE-LIKE EPISODES IN A VIETNAMESE CHILD: CLINICAL, RADIOLOGICAL AND MOLECULAR GENETIC ANALYSIS. Minh Nguyen Khoa Binh Received Received
  P2-213 Heart rate variability in adolescent polycystic ovary syndrome Greek patients Styliani Geronikolou Received Received
  P2-214 CELIAC DISEASE AND ENDOCRINE AUTOIMMUNITY IN CHILDREN AND ADOLESCENTS Feneli Karachaliou Received Received
  P3-214 Central precocious puberty in a 2 year-old with no sinister cause. Sharon Lim Received Received
  P3-215 MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty Berna Ero&287;lu Filibeli Received Received
  P1-215 Acromesomelic dysplasia, type Maroteaux (AMDM): Impact of Long-term (8 years) High-dose Growth Hormone treatment on growth velocity and final height in two siblings Ved Bhushan Arya Received Received
  P2-215 Intestinal ganglioneuromatosis as first manifestation of multiple endocrine neoplasia 2B in a premature girl Tina Leunbach Received Received
  P3-216 Family Central Early Puberty about Three Sisters Mouna Mnif Feki Received Received
  P2-217 Effect of testosterone enanthate therapy on adult height, genital maturation, and bone mineral density in children and adolescents with male hypogonadotropic hypogonadism Hironori Shibata Received Received
  P3-217 Clinical and Molecular Spectrum of Patients with Disorders of Sex Development: A Single Center Experience Samim zen Received Received
  P2-218 The difference of body mass index (BMI) score before and after gonadotropin-releasing hormone agonist (GnRHa) treatment in central precocious puberty girls Yujung Choi Received Received
  P1-218 Lessons from a patient carrying both an 11p paternal duplication and 15q deletion, illustrating the roles of IGF2 and IGF1R in growth regulation FREDERIC BRIOUDE Received Received
  P2-219 Aromatase inhibitor treatment in patient with beta-human chorionic gonadotrophin secreting tumor and gonadotropin-independent precocious puberty. Nadia Mazerkina Received Received
  P3-219 Final adult height in SRY-negative 46,XX ovotesticular differences of sex development individuals. Maria Tereza Ferrari Received Received
  P2-220 Normalized pubertal tempo of maturation and pubertal height gain in girls with MPHD, using a physiological treatment approach with natural estrogens & rhGH. Elena Lundberg Received Received
  P1-220 Real-world data from electronic monitoring of adherence of growth hormone treatment in children with growth disorders: a descriptive analysis Joanna Foley Received Received
  P3-220 A rare cause of SRY (-) 46, XX DSD: Aromatase deficiency TULAY TULAY Received Received
  P3-221 Gonadal dysgenesis, 46 XY about 5 familial cases Mouna Mnif Feki Received Received
  P1-221 Individual patterns of objectively measured adherence to growth hormone treatment and its effect on growth in prepubertal children with growth hormone deficiency Joanna Foley Received Received
  P2-221 The case of congenital hypopituitarism due to mutation POU1F1 in 3 azerbaijani newborn boys. Anzhelika Arestova Received Received
  P2-222 Case report of syndrome of nephrogenic inappropriate antidiuretic hormone secretion (NSIADH) caused by rare AVPR2 gene active mutation wenjing li Received Received
  P1-222 A patient with a novel homozygous mutation in IGF1-R gene and response to growth hormone therapy Azza Nasser Said Al Shidhani Received Received
  P1-223 Tall stature and macrodactyly of the great toes due to a novel variant in the natriuretic peptide receptor 2 gene Danielle van der Kaay Received Received
  P2-223 Long term effects of GnRH agonist therapy on BMI in girls with idiopathic central precocious puberty Dogus Vuralli Received Received
  P3-223 Identification of a de novo mutation in the SRY gene in a 46,XY complete gonadal dysgenesis patient with gonadal neoplasia and review of tumor risk in 46,XY DSD patients Minfei He Received Received
  P2-224 To whom should central nervous system imaging be performed in girls with central precocious puberty (CPP)? Dogus Vuralli Received Received
  P3-224 Clinical and laboratory characteristics of different various types of gonadal dysgenesis in girls with hypergonadotropic hypogonadism Kseniya Kabolova Received Received
  P2-225 Unusual presentation of McCune-Albright syndrome in a 10-year-old girl sara ciccone Received Received
  P1-225 The Phenotypic Spectrum of Kabuki Syndrome in Patients of Chinese Descent YiRou Wang Received Received
  P3-225 Evaluation of the Role of Fetuin A in Pathophysiology of Polycystic Ovarian Syndrome in Adolescents Elvan Bayramoglu Received Received
  P3-226 Rare Cause of 46,XY Sexual Development Disorder: 17-Hydroxysteroid Dehydrogenase Type 3 Deficiency Hayrullah Manyas Received Received
  P1-226 Response to growth hormone in very young children (2 years) with growth hormone deficiency compared with prepubertal children aged =2 years: data from the NordiNet International Outcome Study and ANSWER Program Tilman R Rohrer Received Received
  P2-226 Endocrine transition of care from pediatric to adult medicine in adolescents and young adult survivors of childhood brain tumour. Experience at Hpital Universitaire Necker-Enfants Malades and Hpital Universitaire La Pitié-Salptrière A follow-up study of the 2010-2015 cohort. Laura G. González Briceño Received Received
  P3-227 Persistent elevation of gonadotropins in a girl with aromatase deficiency despite adequate estradiol supplementation- A case for reset hypothalamic-gonadal axis. Neha Agarwal Received Received
  P2-227 Screening of Central Precocious Puberty (CPP) in females: efficacy of morning unstimulated luteinizing hormone (mLH) levels Federico Baronio Received Received
  P1-228 Broadening of the phenotypic spectrum of Coats plus syndrome: a patient presenting with extreme short stature as a hallmark feature. Monique Losekoot Received Received
  P2-228 NEAR ADULT HEIGHT ACCORDING TO GENETIC TARGET AND ABSENCE OF CRANIOFACIAL BONE FIBROUS DYSPLASIA IN A GIRL WITH MC CUNE ALBRIGHT SYNDROME AND GROWTH HORMONE EXCESS: 12.6 YEARS FOLLOW-UP. M. VERONICA FERNANDEZ MENTABERRY Received Received
  P1-229 Endocrine evaluation of 29 Cornelia de Lange Syndrome patients (CdLS) patients ANGELA MARINA ASCASO MATAMALA Received Received
  P3-229 Primary amenorrhea revealing Leydig cell hypoplasia imen gargouri Received Received
  P2-229 Normalized pubertal tempo of masculinisation and pubertal height gain in boys with MPHD, using a physiological treatment approach with low dose testosterone and adequate dose rhGH. Elena Lundberg Received Received
  P3-230 Novel heterozygous mutation in Wilms tumor 1 gene in patient with mixed gonadal dysgenesis Heba Hassan Received Received
  P2-230 The incidence and diagnostic factors of polydipsia and polyuria: a single center survey in Japan Miyuki Kitamura Received Received
  P2-231 Macroprolactinoma presenting with Pituitary Apoplexy associated with middle cerebral artery infarction in an adolescent male. Sally Newbold Received Received
  P3-231 Falsely elevated serum sex steroid hormones in a girl with premature adrenarche Lavinia La Grasta Sabolic Received Received
  P1-231 Height and weight dynamics in preschool boys with constitutional delay of growth and puberty Thomas Reinehr Received Received
  P2-232 Childhood craniopharyngioma: clinical picture at diagnosis in an Italian multicentre study Daniela Driul Received Received
  P1-232 Two Chinese Children with FBN1-Related Acromelic Dysplasia Lele Hou Received Received
  P3-232 NR5A1 Gene Mutation: Variable Phenotypes, New Variants, Different Outcomes Maria Felicia Faienza Received Received
  P3-233 Early embryonic testicular regression syndrome presenting with female external genitalia Sezer Acar Received Received
  P1-233 Growth patterns over two years after birth according to the birth weight and length percentile in children born preterm Seulki Kim Received Received
  P1-234 Identification of syndromal macrosomia: Macrocephaly, but neither height nor weight data are useful in the detection of pediatric PTEN hamartoma Tumor Syndrome (PHTS) Michaela Plamper Received Received
  P3-234 Diagnostic Dilemma in a 46-XY Female Richelle Waldner Received Received
  P2-234 Evaluation of Clinical Features and Treatment Responses of Cases with Hyperprolactinemia servan ozalkak Received Received
  P1-235 Development of a measure for the impacts of pediatricachondroplasia on childrens daily functioning and well-being Jane Beck Received Received
  P2-235 A Case of Gonadotropin-independent precocious puberty due to germ cell tumor in the frontal lobe Bulent Hacihamdioglu Received Received
  P3-235 Leydig Cell Hypoplasia in Three Siblings in the Same Family Hakan Doneray Received Received
  P3-236 KLINEFELTER SYNDROME PRESENTING WITH LEARNING DISABILITIES: CASE REPORTS Paraskevi Zosi Received Received
  P1-236 Serum endocan levels as a marker of endothelial dysfunction in Turner syndrome and correlation with cardiac findings Ali Genco Genay Received Received
  P3-237 Gender self-identification and intra-family relations in children with disorders of sex development Eugenia Globa Received Received
  P2-237 Heterozygous OTX2 deletion in a boy with normal eye development and normal pituitary function. Emese Boros Received Received
  P1-237 The Effects of Fetal Electromagnetic Field Exposure on Expression of Anxiety Behavior and Associated Genes in Adolescent Period Bertan Yilmaz Received Received
  P1-238 Positive correlation between circulating irisin concentrations and homeostatic model assessment for insulin resistance (HOMA-IR) in women with Polycystic Ovary Syndrome: a Meta-analysis FLORA BACOPOULOU Received Received
  P3-238 Bilateral testicular atrophy and normal Inhibin B level : A paradoxal clinical finding for a rare biochemical cause wafa kallali Received Received
  P2-238 Risk Factors for Hypogonadism in Patients with -Thalassemia Major:A Cross-sectional study Zhuan-nan Jiang Received Received
  P1-239 UNUSUAL PRESENTATION OF AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE 1 (APS1) Yagmur Unsal Received Received
  P2-239 Radiation therapy for children with medulloblastoma: Growth and thyroid sequelae. Beatriz Corredor-Andrés Received Received
  P3-239 NORMOSMIC HYPOGONADOTROPIC HYPOGONADISM: AN INTRAFAMILIAR CASE Joana Soares Received Received
  P1-240 Association of Tuberous sclerosis complex (TSC) and Insulinoma in a pediatric patient ANA TANGARI Received Received
  P2-240 Bone age determination in girls with early puberty and limitations of adult height prediction: Can automated evaluation (BoneXpert)be a solution? Gul Yesiltepe-Mutlu Received Received
  P1-241 A novel DCAF17 homozygous mutation in a girl with Woodhouse-Sakati syndrome and its role in the endocrine glands Erdal Kurnaz Received Received
  P2-241 Effect of gonadotropin-releasing hormone agonist treatment on final adult height in boys with idiopathic central precocious puberty EUN-YOUNG KIM Received Received
  P3-242 CLINICAL AND LABORATORY CHARACTERISTICS OF PATIENTS WITH DIFFERENT VARIANTS OF GONADAL DYSGENESIS Ekaterina Sannikova Received Received
  P2-242 Evaluation of the ofalpha2-adrenergic receptors stimulation effect on prolactin secretion, based onthe result of the test with clonidine used in the diagnosis of children withshort stature Renata Stawerska Received Received
  P1-242 Basal metabolic rate in polycystic ovary syndrome: a meta-analysis Styliani Geronikolou Received Received
  P3-243 Etiologic Classification of 46, XY Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results Ayla Guven Received Received
  P2-243 A case of severe recurrent hypoglycemia after traumatic brain injury Dr. Bongsebandhu-phubhakdi Received Received
  P1-243 A nation-wide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in pediatric and adolescent cancer patients Yoko Miyoshi Received Received
  P2-244 The Evolving Role of Whole Exome Sequencing in the Diagnosis of Disorders of Sex Development (DSD) Yardena Tenenbaum-Rakover Received Received
  P3-244 Four-year experience of a new referral center for gender non-conforming children and adolescents in North-East of Italy Gianluca Tornese Received Received
  P1-244 Two Different Endocrine Cancer, One Disease; DICER-1 Mutation Nihal Hatipo&287;lu Received Received
  P2-245 ETIOLOGICAL STRUCTURE DISORDERS OF SEX DEVELOPMENT 46,XY BY ONE CENTER Ekaterina Sannikova Received Received
  P1-245 PTEN Hamartoma Tumor Syndrome (Overlap of Cowden syndrome and the Bannayan-Riley-Ruvalcaba Syndrome): Case Report Hayrullah Manyas Received Received
  P3-245 Ovarian insufficiency: the hidden uterus Biwen Cheng Received Received
  P3-246 An Adolescent Girl Presented with Hoarseness of Voice Ho-chung YAU Received Received
  P1-246 Knowledge of the natural history of paediatric MEN1 is required to inform decision making for predictive testing in childhood Julie Park Received Received
  P2-246 Comparison of growth status, level of blood glucose and lipid metabolism in SGA and AGA girls with central precocious puberty Xi Yang Received Received
  P1-247 One AIRE gene mutation and two different clinical manifestations in a couple of brothers Tiziana Timpanaro Received Received
  P2-247 DOES THE ANOGENITAL DISTANCE PREDICT OUTCOME OF HYPOSPADIAS REPAIR? Alexander Springer Received Received
  P3-247 Turners syndrome mosaicism 45X/47XXX with iron deficiency anemia due to menometrorrhagia Hwal Rim Jeong Received Received
  P3-248 Difficulties in diagnosing variable disorders of sexual development Elena Sukarova-Angelovska Received Received
  P1-248 A novel AIRE gene mutation in two siblings revealing different phenotypes of autoimmune polyendocrine syndrome type 1 Melek Yildiz Received Received
  P1-249 Use of Desmopressin for Bilateral Inferior Petrosal Sinus Sampling (BIPSS) in Pediatric Patients with Cushing Disease (CD). Maria Isabel Di Palma Received Received
  P2-249 11-oxygenated androgens may be related to the virilization of female external genitalia due to the maternal androgen-producing adrenal tumor Keisuke Nagasaki Received Received
  P3-249 Association of Subclinical Hypothyroidism and Dyslipidemia in Children and Adolescents Ashkan Habib Received Received
  P1-250 Correlation between pubertal growth and testicular volume in boys a longitudinal study Anton Holmgren Received Received
  P3-250 Evaluation of Clinical, Demographic Data and Treatment Results of Cases with Graves Disease Ayhan Abac&305; Received Received
  P2-250 High prevalence GnRH receptor mutations in Russian patients with idiopathic hypogonadotropic hypogonadism Elena Frolova Received Received
  P3-251 A case of Graves disease with negative thyrotropin stimulating antibodies in a pediatric patient with type 1 diabetes Liliana Burdea Received Received
  P1-251 Central diabetes insipidus in children: role of GH antibodies Flavia Napoli Received Received
  P2-251 3-HSD2 deficiency due to compound heterozygosity of a missense mutation (p.Thr259Met) and a frameshift deletion (p.Lys273ArgFs7) in an under-virilized infant male with salt wasting. Sofia Leka Received Received
  P2-252 Clinical evaluation of newly developed scoring system for DSD (DSD-SS): Association of DSD-SS with assigned gender in 45,X/46,XY mosaicism Masanobu KAWAI Received Received
  P1-252 Brain Malformations and Sellar Spine as possible causes of Central Precocious Puberty in a large monocentric study Daniela Fava Received Received
  P3-252 An unusual presentation of Hypothyridism: Van Wyk-Grumbach syndrome imen gargouri Received Received
  P2-253 Complexities of diagnosis in 17-beta-hydroxysteroid dehydrogenase deficiency and implementation of next generation sequencing in guiding management decisions Case series of six patients. Tashunka Taylor-Miller Received Received
  P1-253 Changes in the body mass index in children with Central Precocious Puberty under gonadotropin-releasing hormone analogue treatment - a multicentric study. Elisa Galo Received Received
  P3-253 Child thyrotoxicosis Syndrome: Structure and Characteristics. Oleg Latyshev Received Received
  P1-254 A novel approach for the evaluation of hypothalamic-pituitary region in patients with growth hormone deficiency: Pons ratio Edip Unal Received Received
  P2-254 Paediatric Health Assistance to Transsexual Minor in the Multidisciplinary Care Unit of the Basque Country (Spain) Itxaso Rica Received Received
  P3-254 Encephalitis associated with autoimmune thyroiditis : a rare cause of encephalopathy in children. Julie Fudvoye Received Received
  P1-255 Effects of 5-Hydroxymethylfurfural on Pubertal Development of Wistar Rats Selin Elmaogullari Received Received
  P3-255 Association of BMI Z-score and Subclinical Hypothyroidism in Children and Adolescents Ashkan Habib Received Received
  P2-256 A Clinical and cytogenetic study of patients with Disorders of Sex Development (DSDs) Associated with Congenital Anomalies or Recognizable Syndromes inas mazen Received Received
  P1-256 Kisspeptin levels is a new diagnostic approach of hypogonadotropic hypogonadism in boys. Irina Nikitina Received Received
  P3-256 Pseudoprecocious Puberty in a Girl with Untreated Acquired Hypothyroidism Mihaela Dimitrova-Mladenova Received Received
  P1-257 Fetal and post-natal growth are impaired in children with deletions of the GH1 gene: description of a cohort of 14 patients. FREDERIC BRIOUDE Received Received
  P2-257 Efficacy and short-term safety of testosterone treatment in adolescents with gender dysphoria Sabine Hannema Received Received
  P3-257 Bilateral Hip Pain as First Symptomatic Expression of Severe Primary Hypothyroidism ramona nicolescu Received Received
  P3-258 The challenge to treat neonatal autoimmune hyperthyroidism in a small preterm Sarah Lignitz Received Received
  P2-258 Study of Autistic Features among children and adolescents with Congenital Adrenal Hyperplasia Shaymaa Elsayed Received Received
  P1-258 Novel pubertal references for girls using ultrasound to stage breast development. The Bergen Growth Study 2. Ingvild Bruserud Received Received
  P3-259 Graves disease in a 3 year-old patient with agranulocytosis due to methimazole emine demet akba&351; Received Received
  P1-259 Disruption of Hypothalamic regulation of Appetite associated with Proton Beam Therapy aashish sethi Received Received
  P2-259 Differences of sex development with chromosomal mosaicism: histological characterization and immunohistochemistry markers in gonads during childhood. Natalia Perez Garrido Received Received
  P3-260 Hashimotos Thyroiditis in children: Case series report of three patients Thanh Nguyen Trong Received Received
  P2-260 Heterozygous CYP11A1 mutation associated with 46XY Disorder of Sexual Differentiation and mild Adrenal Insufficiency Philippa Bowen Received Received
  P1-260 A case-control study of exposure to bisphenol-A and phthalates in girls with early onset of puberty annalisa deodati Received Received
  P1-261 Long-term urological and psychosexual outcome of men born with hypospadias Lloyd Tack Received Received
  P3-261 Mutation of RET gene causes multiple endocrine neoplasia type 2B in an Adolescent: report of one case and literature review Yuan Xiao Received Received
  P2-261 The modern approaches to differential diagnosis of constitutional delay of puberty and hypogonadotropic hypogonadism in boys Oleg Latyshev Received Received
  P3-262 A 12 year old boy with multifocal papillary thyroid carcinoma Nataliia Muz Received Received
  P2-262 Etiologic Classification of 46, XX Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results Ayla Guven Received Received
  P1-262 Long-Term Outcome In Leydig Cell Hypoplasia Alessandra Boncompagni Received Received
  P2-263 Novel genotype in two siblings with 5-alpha-reductase 2 deficiency:different clinical course due to the time of diagnosis Mirjana Kocova Received Received
  P3-263 Papillary Thyroid Cancer in Children: Single Center Results gl direk Received Received
  P1-263 Genotype-Phenotype Correlation of SRD5A2 Gene Variants in 130 Chinese Children: Based on a Chinese High-Homogeneity Single-Center Cohort Lijun Fan Received Received
  P2-264 Ethical and familial dilemmas of genitoplasty encountered in Congenital Adrenal Hyperplasia Dirlewanger Mirjam Received Received
  P1-265 Dynamics in blood pressure after pubertal suppression with GnRH analogs followed by testosterone treatment in male adolescents Liat Perl Received Received
  P2-265 Hormonal assessment of malformation syndromes associated with disorders of sex development: Case series of 9 patients Shaymaa Mahfouz Received Received
  P3-266 A Novel Mutation of INSR Gene in a Child with Type A Insulin Resistance Federica Verdecchia Received Received
  P1-266 A Nationwide Study Of The Prevalence & Initial Management Of Atypical Genitalia & Delayed Sex Assignment In The Newborn Salma Ali Received Received
  P2-266 Family Perrault syndrome in two Tunisian sisters Mouna Mnif Feki Received Received
  P2-267 An intriguing co-occurrence of MURCS and VACTER associations Noa Shefer Averbuch Received Received
  P3-267 INDEXES OF ADIPOSITY AND BODY COMPOSITION IN THE PREDICTION OF METABOLIC SYNDROME IN OBESE CHILDREN AND ADOLESCENTS: WHICH IS THE BEST? Fiorenzo Lupi Received Received
  P1-267 Endocrine profiling and association with testicular volume and biometrics in a cohort of Norwegian boys Andre Madsen Received Received
  P3-268 Clinical, Laboratory and Radiological Assessment of Obese and Non-Obese Girls Evaluated for Early Puberty Deniz Ozalp K&305;z&305;lay Received Received
  P1-268 Idiopathic scoliosis in girls with central precocious puberty: Incidence and effect of gonadotropin-releasing hormone agonists Lindsey Yoojin Chung Received Received
  P2-269 Pseudo-precocious puberty in children triggered by incidental transdermal contamination with topical sex steroids through parents Vira Yakovenko Received Received
  P3-269 IGSF1 mutation: treatment in the absence of symptoms? Sarah Castets Received Received
  P1-269 The impact of Klinefelter Syndrome on quality of life a multicentre study Sebastian Franik Received Received
  P1-270 Large spectrum of DSD phenotype caused by pathogenic variants in Wilms tumor suppressor gene 1. Maria Tereza Ferrari Received Received
  P3-270 Real World Experience of Burosumab Therapy in Children with X-linked Hypophosphataemic Rickets - 12 month follow-up data Jessica Sandy Received Received
  P2-270 FOLLOW-UP OF INDIVIDUALS WITH GENDER IDENTITY DISORDERS: A LONG AND CHALLENGING PROCESS Esin Karakilic Ozturan Received Received
  P3-271 Psychosocial wellbeing of parents and quality of life of children (QoL) with 46, XY Disorders of Sex Development (DSD) attending the endocrine clinics at Lady Ridgeway Hospital (LRH) for children Dilusha Gangoda Liyanage Received Received
  P2-271 Follow-up of two similar patients with Steroidogenic Factor-1 (SF-1/ NR5A1) variants, in two different eras Odile Gaisl Received Received
  P1-271 Endocrine and reproductive outcome of men born with various degrees of hypospadias Lloyd Tack Received Received
  P1-272 Age at menarche over the last decades and inter-regional variability in Northern Spain Pablo Alonso Rubio Received Received
  P2-272 Genetic testing of DSD patients in Ukraine Eugenia Globa Received Received
  P1-273 Hypergonadotropic hypogonadism in 46, XX adolescents without gonadotoxic therapy: Clinical features and molecular etiologies Zehra Yavas Abali Received Received
  P2-273 Spectrum of genital abnormalities in Robinow syndrome: Case series. Shaymaa Mahfouz Received Received
  P3-273 THE INCREASE IN ADIPOSE TISSUE DURING GH TREATMENT INDUCES INSULIN RESISTANCE Zvi Laron Received Received
  P2-274 MAMLD 1 gene mutation and 46 XY sex development disorder : a case report BOUCHRA BOUSYF Received Received
  P1-274 Quality of life in Chilean transgender children, adolescents, and their parents Carolina Mendoza Received Received
  P3-274 Role of adiposity indexes in the risk of ketoacidosis (DKA) in children with type 1 diabetes (T1D) at onset Valeria Castorani Received Received
  P3-275 Serum spexin is correlated with lipoprotein(a) and androgens in normal-weight, overweight and obese adolescent females FLORA BACOPOULOU Received Received
  P2-275 46,XYcomplete gonadal dysgenesis in a familial case with a rare mutation in theDesert Hedgehog (DHH) gene Vassos Neocleous Received Received
  P1-275 Long-term outcome of testicular function in nonclassic lipoid congenital adrenal hyperplasia Tomohiro Ishii Received Received
  P3-276 Exocrine pancreatic insufficiency and vitamin K deficiency associated to Octreotide therapy in congenital hyperinsulinism: An under-recognized potential adverse effect. PURIFICACIÓN ROS-PÉREZ Received Received
  P2-276 Novel thyroid hormone receptor -gene mutations in resistance to thyroid hormone Ga Hyun Lee Received Received
  P2-277 Congenital Hypothyroidism: neonatal screening program with T4 and TSH. Maria Chueca Received Received
  P3-277 The Role of Urine AVP in the Diagnostic Pathway of Polyuria and Polydipsia Syndrome Claudio Giacomozzi Received Received
  P2-278 A 10- year-old girl with thyroid hormone resistance (THR)- case report. Artur Bossowski Received Received
  P3-278 NEW MUTATION OF GNAS IN A 2 YEAR OLD ONCOLOGICAL PATIENT Ana Belen Ariza Jimenez Received Received
  P3-279 Relation between levels of atymullerian hormone and inhibin B and spontaneous puberty in patients with Turner syndrome preliminary results Anna Rusza&322;a Received Received
  P2-279 DIAGNOSIS OF CENTRAL CONGENITAL HYPOTHYROIDISM AND MULTIPLE PITUITARY DEFICIENCIES THROUGH A NEONATAL SCREENING PROGRAM. Gema Grau Received Received
  P1-279 Gender mender, or defender: Understanding decision making in Aotearoa/New Zealand for people born with a variation in sex characteristics. Esko Wiltshire Received Received
  P2-280 CHILDHOOD THYROID CANCER AFTER RADI OIODINE THERAPY OUIDAD BAZ Received Received
  P3-280 Short, but daily and controlled physical activity of children with obesity has a positive effect on the irisin and chemerin levels Ma&322;gorzata Wójcik Received Received
  P2-281 Differential diagnosis of euthyroid hyperthyroxinemia Eugenia Globa Received Received
  P3-281 New Autosomal Dominant Mutation in Glucokinase Gene Causing Congenital Hyperinsulinism Diagnosed in Adulthood Ilana Zalmon-Koren Received Received
  P1-281 Virilization of a girl at puberty due to a unique translocation of an abnormal duplicated Y-chromosome to a deleted chromosome 9 including the DMRT1 gene Stefanie Graf Received Received
  P1-282 Characteristics of 311 children with early onset pubertal signs. Descriptive study paula sol ventura wichner Received Received
  P2-282 Treatment for Graves Disease in Children and adolescents: A Long-Term Retrospective Study at a Single Institution Min-Sun Kim Received Received
  P3-283 COMPARISON OF DENSITOMETRIC ASPECTS DURING THE TRANSITION PERIOD IN PATIENTS WITH CONGENITAL AND ACQUIRED PITUITARY DEFICIENCY: FIRST ARGENTINE EXPERIENCE. HUGO BOQUETE Received Received
  P2-283 Changes of thyroid function in girls with central precocious puberty after 6-month GnRH agonist treatment Young-Jun Rhie Received Received
  P1-283 Children with Hashimotos thyroiditis have increased intestinal permeability: Results of a pilot study Banu Kucukemre Aydin Received Received
  P1-284 Different Endocrine Affects in DICER-1 Syndrome semra etinkaya Received Received
  P2-284 Papillary Thyroid Cancer Associated With Hyperthyroidism AHU PAKET&304; Received Received
  P3-284 Demographic, clinical and biochemical characteristics of pediatric obesity: interim analysis of a larger prospective study Maja Tankoska Received Received
  P3-285 Mental health of both child and parents play a larger role in health related quality of life of obese and overweight children Deniz Ozalp K&305;z&305;lay Received Received
  P1-285 Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases AHU PAKET&304; Received Received
  P2-285 Serum PTH does not correlate with their serum calcium levels in children and adolescents with Hashimoto thyroiditis Hirohito Shima Received Received
  P2-286 Management of childhood thyroid nodules in children a large group of cases from a single center. Joanna Sieniawska Received Received
  P3-286 Alterations in ambulatory blood pressure in adolescents with obesity. Desiree LOPEZ-GONZALEZ Received Received
  P1-286 Identification of a THRA mutation in a 2yr old child with clinical features of hypothyroidism and multisystem involvement Rajesh Sakremath Received Received
  P1-287 The comparison of natural course thyroid autoimmunity in children and adults with type 1 diabetes: from the diabetes onset up to five years of its duration. Elzbieta Niechcial Received Received
  P3-287 Should we review clinical criteria to diagnose SHOX gene mutations? Francesco Gallo Received Received
  P2-287 BONE HOMEOSTASIS IN CHILDREN WITH SUBCLINICAL HYPOTHYROIDISM: EFFECTS OF TWO-YEARS TREATMENT WITH LEVOTHYOXINE Flavia Barbieri Received Received
  P1-288 Outcomes of persistent hyperthyrotropinaemia in well term infants May Ng Received Received
  P3-288 Circulating chemerin may be associated with early vascular pathology in obese children without overt arterial hypertension preliminary results Ma&322;gorzata Wójcik Received Received
  P1-289 Thyroid peroxidase antibodies in children with HLA-conferred susceptibility to type 1 diabetes Liisa Saare Received Received
  P3-289 Quality of Life of patients with Type 1 Diabetes. Renata Markosyan Received Received
  P1-290 Prediction of permanent and transient congenital hypothyroidism based on levothyroxine dosages in long-term follow-up patients: a multicenter retrospective study in Japan Shinji Higuchi Received Received
  P2-290 A rare combination with Congenital Hypothyroidism - Brain Lung Thyroid Syndrome Sajith Sandamal Received Received
  P3-290 Etiologies and clinical patterns of Hypopituitarism in Sudanese children Samar Hassan Received Received
  P1-291 An incidental finding of thyroid hormone resistance due to a de novo mutation in the THRB gene Noa Shefer Averbuch Received Received
  P3-291 Rare causes for paediatric virilizing tumors Jananie Suntharesan Received Received
  P1-292 Outcome of congenital hypothyroidism in Algeria: the urgent need to implement a national newborn screening program Adel DJERMANE Received Received
  P2-292 Thyroid autoimmunity in children and adolescents with Type 1 Diabetes Mellitus Nalini M Selveindran Received Received
  P3-293 Clinical evolution of a patient with isolated growth hormone deficiency type IA treated with rIGF1 for 5 years after the development of GH-antibodies. Albert Feliu Received Received
  P2-293 Analysis of diabetes-associated autoantibodies in children and adolescents with autoimmune thyroid diseases Artur Bossowski Received Received
  P3-294 Beck Depression inventory scores for children with some chronic diseases (Type I diabetes mellitus, Sickle cell anaemia, and AIDS) in University of Port Harcourt Teaching Hospital Iroro Yarhere Received Received
  P1-296 Three novel mutations of the StAR gene in five Algerian patients presenting with classical and non-classical lipoid adrenal hyperplasia. Asmahane Ladjouze Received Received
  P3-296 Neonatal severe hyperparathyroidism - using genetics to determine treatment Carmit Avnon-Ziv Received Received
  P2-296 Progressive thyroid dysfunction in infants with Down Syndrome; Trisomy 21 (DS): Effect on Linear Growth Nada Alaaraj Received Received
  P2-297 EVALUATION OF ELEVATED SERUM THYROID-STIMULATING HORMONE (TSH) IN CHILDREN AND ADOLESCENTS: A SINGLE-CENTER STUDY IN URUGUAY. Mariana Risso Received Received
  P1-297 A novel compound heterozygous mutation in the CYP11B2 gene, including an intron 7 splice site, is responsible for aldosterone synthase deficiency type II Jianfang Zhu Received Received
  P3-297 LIVER TRANSPLANTATION IN SAUDI HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA PATIENTS Salman Al-Mansour Received Received
  P3-298 Mitchell-Riley Syndrome, a report of novel mutation in a Palestinian family resulting in Neonatal diabetes Abdulsalam Abu-Libdeh Received Received
  P1-298 First morning pregnanetriol and 17-hydroxyprogesterone correlated significantly each other with in 21-hydroxylase deficiency Tomoyo Itonaga Received Received
  P2-298 Neonatal hyperthyroidism: our centres experience Silvana Caiulo Received Received
  P3-299 Review of neonatal cortisol evaluation between 2012-2018 in a single centre: trends, outcomes and associations. Taffy Makaya Received Received
  P2-299 Epidemiological aspects of pediatric thyroid disorders in Western Ukraine Viktoriya Furdela Received Received
  P1-299 Medical identification jewellery use in children and young adults with adrenal insufficiency Georgina Chrisp Received Received
  P3-300 Height and Upper/Lower Body Ratio in Turner Syndrome Adolescents in Indonesia; Is There Any Significant Difference Based on Karyotype? Novina Novina Received Received
  P1-300 Growth trajectory and final height in children with non classical congenital adrenal hyperplasia Letteria Anna Morabito Received Received
  P2-300 The encephalopathy as complication of Hashimoto thyroiditis in children: a wide variety of clinical manifestations Paola Chiarello Received Received
  P2-301 Acute-onset peripheral polyneuropathy in a 12-year-old girl due to Hashimoto thyroiditis: traps in the diagnosis Assimina Galli-Tsinopoulou Received Received
  P3-301 A novel heterozygous mutation in the SLC5A2 gene causing mild failure to thrive and subclinical hypoglycemia in a 2-year old girl DIMITRIOS PAPADIMITRIOU Received Received
  P1-301 Height in Infants aged 1 year with classic Congenital Adrenal Hyperplasia is related to their urinary Steroid Metabolome Clemens Kamrath Received Received
  P3-302 Cognitive and Learning Performance of Children and Adolescents Cancer Survivors FLORA BACOPOULOU Received Received
  P1-302 MIRAGE: A Novel Syndromic Form of Primary Adrenal Insufficiency (PAI) Xinyi Chin Received Received
  P3-303 Hirsutism in children: pitfalls and diagnostic challenges Teofana-Otilia Bizerea-Moga Received Received
  P3-304 Congenital craniopharyngioma - A rare case of congenital hypopituitarism. Jananie Suntharesan Received Received
  P3-305 Combined Surgical and Medical Treatment in an Adolescent with Severe Gynecomastia Due to Excessive Estradiol Secretion: A case report Miseon Lee Received Received
  P1-305 Clinical Manifestations & Molecular analysis of four Palestinian patients with Pseudohypoaldosteronism type 1 (PHA 1) revealing Four novel mutations in the ENaC subunit genes Abdulsalam Abu-Libdeh Received Received
  P3-306 IMPROVEMENT OF METABOLIC CONTROL IN CHILDREN WITH TYPE1 DIABETES USING CONTINUOUS GLUCOSE MONITORING DEVICES Estela Gil-Poch Received Received
  P1-306 Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience gizem cilsaat Received Received
  P1-307 CAH-X due to homozygous deletions of CYP21A2 and TNXB exon 35 in a newborn from the 17 OHP screening Kalina Mihova Received Received
  P3-307 Autoimmune thyroiditis in beta thalassemia major after the hematopoietic stem cell transplantation - case report Maja Tankoska Received Received
  P3-308 Graves disease: what place in the childs hyperthyroidism? mohamed samir merad Received Received
  P1-308 ABCC8 MODY in an Obese Adolescent Misdiagnosed with Type 2 Diabetes Berna Ero&287;lu Filibeli Received Received
  P1-309 Level of glycemic control in pediatric patients with type 1 diabetes in Bern: a cross-sectional study Tanja Zingg Received Received
  P3-309 Vitamin D status among children and adolescents in an Egyptian cohort: can we predict vitamin D deficiency? Mona Karem Received Received
  P1-310 Preliminary results of public health prevention program for diabetic ketoacidosis in children and adolescent Marko Simunovic Received Received
  P3-310 CASE REPORT: Primary Hyperparathyroidism Presenting as a Brown Tumor of Mandible in an Adolescent Girl - An Unusual presentation with Challenges and Outcome Jaida Manzoor Received Received
  P3-311 Serum Calcium, 25(OH) vitamin D and Bone alkaline phosphatase in children with epilepsy receiving antiepileptic drugs in University of Port Harcourt Teaching Hospital Iroro Yarhere Received Received
  P1-311 Optimisation of transfection methods using DNA, RNA and Protein Formats for CRISPR Cas9 mediated gene knock out in Beta-TC-6 cells. Preetha Purushothaman Received Received
  P1-313 Familial versus non-familial type-2 diabetes mellitus in children and adolescents: Clinical and Biochemical Data. fawziya Alyafei Received Received
  P3-314 Case report: Hyperglicemic iperosmolar state in a obese prepubertal girl with newly diagnosis of type 2 diabetes Nella Polidori Received Received
  P3-315 Associations between pituitary abnormalities and treatment response in children with growth hormone deficiency. First multicenter study in Portugal Catarina Diamantino Received Received
  P1-316 An evaluation of the accuracy of a flash glucose monitoring system in children with diabetes in comparison with venous blood glucose Bingyan Cao Received Received
  P3-316 Epidemiological and socioeconomic CHANGES in the child population from debut DM1 in this 21st century Ignacio Diez Received Received
  P1-317 Unexplained neonatal deaths among Kurdish consanguineous families: Importance of recognizing congenital hyperinsulinism and testing for KATP channel gene variants Shenali Anne Amaratunga Received Received
  P3-317 Body Mass Index and Incident Type 1 Diabetes in Children from Lesser Poland over an 11 year observation period Ma&322;gorzata Wójcik Received Received
  P3-318 Novel mutation in HNF4-alpha gene and reclassification of diabetes in a family Maria Miguel Gomes Received Received
  P3-319 Systemic lupus erythematosus, Celiac and Hypothyroidism complicating type 1 diabetes: a rare tetrad. Rakhi Jain Received Received
  P1-319 Gene dosage changes in the GCK gene not detected by Sanger DNA sequencing in two patients with phenotypic MODY 2 Niels Birkebaek Received Received
  P1-320 Assessment of Vascular Endothelial Dysfunction Using Brachial Artery Flow Mediated Dilatation and Carotid Intima Media Thickness in Children and Adolescents with Type 1 Diabetes Shereen Abdelghaffar Received Received
  P3-320 EpiPEG-PreMeb study: chemerina plasmatic and metabolic syndrome relation at SGA childrens Ignacio Diez Received Received
  P1-321 A Case of Late-Onset Monogenic Diabetes Due to a Homozygous Variant in the GCK Gene Berna Ero&287;lu Filibeli Received Received
  P3-321 Hydrometrocolpos due to congenital adrenal hyperplasia A rare cause of bladder outflow tract obstruction in a female child Jananie Suntharesan Received Received
  P3-322 Bartter syndrome complicated with growth hormone deficiency due to a suprasellar arachnoid cyst. Fathima Raihana Hashim Received Received
  P1-322 Neonatal diabetes and Glis3 mutation: a new phenotype Sana Kmiha Received Received
  P1-323 Diabetes type 2 in non-obese neurologically impaired children and adolescents: a new emerging entity? Valeria Calcaterra Received Received
  P3-324 Hypoglycemia in a patient with Turner syndrome and Kabuki make-up ziqin liu Received Received
  P1-324 Cataract in type 1 diabetes mellitus patients- a nationwide population-based study Li-Min Chen Received Received
  P3-325 45X/47XXX Mosaicism and progressive puberty ziqin liu Received Received
  P1-325 Association of CTLA-4 gene with the familial diabetes mellitus Talat Saatov Received Received
  P3-326 VITAMIN D AND TYPE 1 DIABETES MELLITUS IN CHILDREN Harjoedi Adji Tjahjono Received Received
  P1-326 Copy Number Variation (CNV) Sequencing Identifies a Novel Mutation of the Glucokinase Gene in Maturity-onset Diabetes of the Young Yan Li Received Received
  P1-327 The Paediatric Diabetes Service in England and Wales Learning from Swedens Improvement Journey. Megan Peng Received Received
  P3-327 Severe hypercalcaemia after years on the ketogenic diet: A novel case report Jessica Sandy Received Received
  P1-328 Creating a neural network model based on glycemic variability indices to predict the degree of compensation for type 1 diabetes Marina Koshmeleva Received Received
  P3-328 Estrogen Production by Sertoli cell tumor in unusual case of Testicular feminization syndrome shahab noorian Received Received
  P3-329 Dysphagia and dyspnea by lingual thyroid mass in a young child: what to do? mohamed samir merad Received Received
  P1-329 Evaluation of AGP reports in patients with type 1 diabetes using intermittently viewed continuous glucose measurement system (iCGM) Erdal Eren Received Received
  P1-330 Evaluation of Clinical, Laboratory and Therapeutic Features and Long Term Follow-up Results in 44 Cases with Genetic Diagnosis of MODY; Single Center Experience servan ozalkak Received Received
  P3-330 Van-Wyk Grumbach syndrome associated with trisomy 21: a case report Nihad Selim Received Received
  P3-331 Fahr syndrome in young boy with hypoparathyroidism. mohamed samir merad Received Received
  P1-331 DESIGN AND IMPLEMENTATION OF AN INTEGRAL SYSTEM OF CLINICAL FOLLOW-UP AND GLUCOSE MONITORING IN CHILDREN AFFECTED OF TYPE 1 DIABETES, IN ANDALUSIA. María Rocío Hernández-Soto Received Received
  P3-332 Thyroid cancer in a child with gravess disease mohamed samir merad Received Received
  P1-332 Targeted next-generation sequencing demonstrates high frequency of MODY in Russian children. Natalia Zubkova Received Received
  P3-333 Influence of nocturnal hypoglycemia on school performance of teens with DM type1 Ignacio Diez Received Received
  P1-335 The relationship between serum neurotensin levels and metabolic parameters and eating behavior in obese children Gnl atl&305; Received Received
  P1-337 How does Clusters of Parental Characteristics Influences Offspring Adiposity: A Prospective Study Marina Ybarra Received Received
  P1-338 CONTINUOUS SCORE OF METABOLIC SYNDROME (sSMp) IN CHILEAN PEDIATRIC POPULATION IS ASSOCIATED WITH INSULIN RESISTANCE PARAMETERS AND SUBCLINICAL ENDOTHELIAL INFLAMMATION. Carolina Loureiro Received Received
  P1-339 Elevated high-sensitivity C-reactive protein level is associated with prediabetes and adiposity in Korean children and adolescents. Sohyun Shin Received Received
  P1-341 ANGPTL2 and ANGPTL3 in children with obesity and metabolic syndrome Maryam Razzaghy Azar Received Received
  P1-342 Can Increased First Hour Glucose Concentration in OGTT Be a New Indicator in Projecting Metabolic Profile? Servan zalkak Received Received
  P1-343 Perinatal features of Prader-Willi syndrome: a Chinese cohort Lili Yang Received Received
  P1-346 Non-invasive assessment of liver steatosis: usefulness of elastography in obese children a pilot study. Domenico Corica Received Received
  P1-347 PRECOCIOUS PUBARCHE IN SPINAL MUSCULAR ATROPHY PATIENTS WITH SEVERE SARCOPENIA Avivit Brener Received Received
  P1-348 EVALUATION OF THE RELATIONSHIP BETWEEN SERUM URIC ACID LEVEL AND CARDIOMETABOLIC RISK IN OBESE CHILDREN AND ADOLESCENTS Servan zalkak Received Received
  P1-349 Prevalence of dyslipidemia in Korean youth over 10 years: data from the Korea National Health and Nutrition Examination Survey 2008-2017 JIEUN LEE Received Received
  P1-350 Metabolic risk in long-term survivors of childhood acute lymphoblastic leukemia Milena Belcheva Received Received
  P1-351 Congenital generalized lipodystrophy type 4 - New mutation in the CAVIN1 gene Esra Dger Received Received
  P1-352 Paediatric patients with type 1 diabetes mellitus exhibit reduced brown adipose tissue heat signature following cold stimulation James Law Received Received
  P1-354 Association between adiposity measures and metabolic variables in children and adolescentswith obesity Giuseppina Rosaria Umano Received Received
  P1-355 A comparison of insulinresistance indices: HOMA and Belfiore in 6-8-year-old, properly growingchildren, born small for gestational age ANNA LUPINSKA Received Received
  P1-356 The double diabetes in adolescent with Prader-Willi syndrome. Elena Bogova Received Received
  P1-357 Evaluation of body composition and resting metabolic rate in adolescents with KS Daria Bespaliuk Received Received
  P1-358 Relationship between RBP4 level and two of its gene polymorphisms with body composition and metabolic profile in obese children Ionela Pascanu Received Received
  P1-359 Insulin-like growth factor 2 in pediatric gliomas: expression, intracellular localization and association with clinical outcome FLORENCIA CLÉMENT Received Received
  P1-360 Prevalence of children born small for gestational age with short stature who qualify for growth hormone treatment: a preliminary population-based study Gianluca Tornese Received Received
  P1-361 Long-term Safety of a once-weekly Somatrogon (hGH-CTP): 4-Year Results of a Phase 2 Extension Study in Children with Growth Hormone Deficiency Aleksandra Pastrak Received Received
  P1-363 Metabolism of somapacitan, a long-acting growth hormone derivative, in human subjects Birgitte Damholt Received Received
  P1-364 GH Values In Serum And Blood Spots On Filter Paper Samples In Neonates Until 30 Days Of Life By Electrochemiluminescence (ECLIA). Mirta Miras Received Received
  P1-365 De novo formation of neutralizing IGF-I antibodies during rhIGF-1 treatment in a girl with IGFALS deficiency as distinct adverse event interfering with growth promotion Janna Mittnacht Received Received
  P1-366 Glomerular filtration rate in young adults born SGA: a 5-year longitudinal study after cessation of GH treatment. Wesley Goedegebuure Received Received
  P1-367 Normal IGF-bioactivity and low free IGF-I in patients with Prader-Willi syndrome with high total serum IGF-I: immunoreactive IGF-I concentration poorly reflects IGF bio-activity and bio-availability. Karlijn Pellikaan Received Received
  P1-369 Detection and referral of children with short stature in Serbia - the impact of electronic growth charts Sanja Panic Zaric Received Received
  P1-370 Challenges experienced in delivering growth hormone therapy in childrens with Prader Willi syndrome in Birmingham Childrens Hospital. D. Udeni Anuruddhika Kollurage Received Received
  P1-371 Growth Hormone Deficiency (GHD): Assessing Parent Burden for Child Growth Hormone Deficiency Treatment: the Growth Hormone Deficiency - Parent Treatment Burden Measure (GHD-PTB) Meryl Brod Received Received
  P1-373 Matrix metalloproteinases, their inhibitors and neurotrophic factors as indicators of cardiometabolic risk in Turner syndrome girls Ewa B&322;aszczyk Received Received
  P1-374 Growth in the first ten years after Antiretroviral Therapy initiation among HIV-infected children in the CoRISpe spanish pediatric cohort. Jesus Dominguez Riscart Received Received
  P1-375 SOAR Study: New approaches to managing social skills deficits in Turner Syndrome Jeanne Wolstencroft Received Received
  P1-376 Noonan Syndrome (NS) spectrum panels should include mutations in LZTR1 gene Maria Guemes Received Received
  P1-377 International consensus: Ovarian tissue cryopreservation in young Turner syndrome patients. Outcomes of an ethical Delphi study including 55 experts from 16 different countries. Sapthami Nadesapillai Received Received
  P1-378 Vascular Anomalies And Aortic Dilatation in Turner Syndrome Study In A Large Cohort Of Young-Adult Patients Laura Mazzanti Received Received
  P1-379 Adult height prediction by bone age determination in children with idiopathic growth hormone deficiency (IGHD): Analysis of KIGS data. Thomas Reinehr Received Received
  P1-380 A new model of adult height prediction validated in boys with constitutional delay of growth and puberty Thomas Reinehr Received Received
  P1-381 The relation between Changes in Body Mass Index (BMI) and linear growth in prepubertal children: Daily Weight Gain and BMI changes in Relation to Linear Growth During Nutritional Rehabilitation of Underweight Children. Ashraf Soliman Received Received
  P1-382 NUTRITIONAL REQUIREMENTS IN PRADER WILLI SYNDROME CHILDREN TREATED WITH GROWTH HORMONE UNDER TWO YEARS OF AGE Raquel Corripio Received Received
  P1-383 Cardiovascular Anomalies and Association with Karyotypes in Turner syndrome in Taiwan: one medical center experience FU-SUNG LO Received Received
  P1-384 Pubertal induction amongst girls with Turner Syndrome: a review of changing practice over 10 years. Hassan Elechi Received Received
  P1-386 Prevalence of copy number variations (CNVs) in a cohort of SGA children with persistent short stature associated with additional clinical features. elena inzaghi Received Received
  P1-388 Is there a QTc interval prolongation in girls and women with Turner syndrome? Iris Noordman Received Received
  P1-389 Eight years of growth hormone treatment in a patient with Schaaf-Yang Syndrome Alicia Juriaans Received Received
  P1-390 Genetic Evaluation of Idiopathic Short Stature Firdevs Bas Received Received
  P1-391 Foramen magnum stenosis (FMS): neuroradiological aspects before and after cervical decompression in paediatric patients with achondroplasia (ACH).The Achondroplasia Multidisciplinary Gaslinis Group (AMGG) Istituto Giannina Gaslini, Genova, Italy: Child Anna Elsa Maria Allegri Received Received
  P1-392 Do children and adolescents with idiopathic short stature show postural alterations? Possible influence of SHOX haploinsufficiency in a pilot study Maria Cristina Maggio Received Received
  P1-393 Evaluation of body composition and resting metabolic rate in children with growth hormone deficiency Maria Pankratova Received Received
  P1-395 Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years Johanna Hietamki Received Received
  P1-397 Questioning the Value of Brain MRIs in the Evaluation of Children with Isolated Growth Hormone Deficiency Ori Eyal Received Received
  P1-398 Postoperative Quality of Life in Children and Adolescents with Craniopharyngioma Results of the prospective multicenter trial KRANIOPHARYNGEOM 2007 Hermann L. Muller Received Received
  P1-399 Pubertal events, reproductive and growth hormones and predictive factors in healthy girls with Transient Thelarche. JULIO SOTO Received Received
  P1-400 PLASMA COPEPTIN DISTRIBUTION IN THE PEDIATRIC AGE: A USEFUL DIAGNOSTIC TOOL FOR AVP-RELATED DISORDERS Gerdi Tuli Received Received
  P1-401 Management and treatment outcome of childhood-onset craniopharyngioma (CP) in Italy: multicentre collection of 117 cases Stefano Zucchini Received Received
  P1-402 EVALUATION OF BRAIN MRI LESIONS IN 381 GIRLS WITH CENTRAL PRECOCIOUS PUBERTY didem helvac&305;o&287;lu Received Received
  P1-403 Xanthomatous hypophysitis : a rare case in a paediatric patient Sze Lyn Jeanne Wong Received Received
  P1-404 Improvement of final height in idiopathic central precocious puberty is associated with delay of bone maturation with GnRH agonisttherapy under the age of 7 years Dogus Vuralli Received Received
  P1-406 Tolvaptan for management of intractable salt and water imbalance in a case with suprasellar tumor after surgery Tomoe Yamaguchi Received Received
  P1-407 No association between serum level of NPTX 1 and MKRN3 in central precocious puberty Hwal Rim Jeong Received Received
  P1-408 Training in pubertal assessment First step to the observational pilot study PROSPEL (Premier Observatoire des Stades Pubertaires en Libéral) monique Perelroizen Received Received
  P1-409 LONG-TERM OUTCOME IN YOUNG WOMEN TREATED FOR CENTRAL PRECOCIOUS PUBERTY Ida DAcunzo Received Received
  P1-410 Sertoli cell function after chemotherapy in boys with hematologic malignancies Romina Grinspon Received Received
  P1-412 WES analysis of a cohort of 94 patients presenting with 46,XY and 46,XX DSD Patrick Sproll Received Received
  P1-413 Assessment of the Function of Lower Urinary Tract Following Feminizing Genitoplasty in Females with Congenital Adrenal Hyperplasia Shaymaa Elsayed Received Received
  P1-414 Gonadal Insufficiency and Affecting Factors in Patients with Bone MarrowTransplantation(BMT) for Non-malignantIndications in Childhood or Adolescence Samim zen Received Received
  P1-415 Clinical and Molecular Characteristics of Russian Patients with 46,XY DSD due to NR5A1 Gene Mutations. Natalia Kalinchenko Received Received
  P1-416 Creating a clinicalevaluation system for simple and comprehensive scoring of differences/disorders of sexual development Fusa Nagamatsu Received Received
  P1-418 Epidemiology of diagnoses of Sex Development Disorders based on the Registry of rare diseases, in a large area of North-Eastern Italy LAURA GUAZZAROTTI Received Received
  P1-419 Premature ovarian insufficiency in women after treatment for childhoodcancer is a risk factor for metabolic syndrome Axel Netterlid Received Received
  P1-420 The Genetic and Clinical Characteristic of Pediatric Patients with Congenital Hypothyroidism Gland In-Situ Maria Cristina Vigone Received Received
  P1-421 Zinc transporter 8 (ZnT8) as a new autoantigen in thyroid tissue preliminary data Artur Bossowski Received Received
  P1-422 PROSPECTIVE EVALUATION OF AUTOIMMUNE AND NON-AUTOIMMUNE SUBCLINICAL HYPOTHYROIDISM IN A LARGE COHORT OF CHILDREN AND ADOLESCENTS WITH DOWN SYNDROME Giorgia Pepe Received Received
  P1-423 Congenital hypothyroidism (CH) detected by the second newborn screening in Lombardia region: incidence and evolution of CH Silvana Caiulo Received Received
  P1-424 Transition for patients with chronic thyroid diseases Piriya Ratnasabapathy Received Received
  P1-425 Maternally inherited resistance to thyroid hormones with discordant postnatal phenotypes in two infant brothers Rosalie Cavin Received Received
  P1-426 A rare case of familial heterozygous Thyroid hormone receptor beta (THRB) mutation presenting with dilated cardiomyopathy Lucy Hastings Received Received
  P1-427 Acquired Hypothyroidism in a Toddler: An Unusual Presentation of Langerhans Cell Histiocytosis Richelle Waldner Received Received
  P1-428 Anti-gastric parietal cells antibodies for autoimmune gastritis screening: a follow-up study in young patients with autoimmune thyroid disease. Valeria Calcaterra Received Received
  P1-429 Genetic evaluation of congenital hypothyroidism with gland-in-situ using targeted exome sequencing Jung hyun shin Received Received
  P1-430 Clinical Characteristics and Long-term Follow-up of Patients with Congenital Hypothyroidism (CH) due to Thyroid Peroxidase (TPO) gene Mutations Leraz Tobias Received Received
  P1-431 The relationship between perfluoroalkyl compounds concentrations at ages 2, 4, and 6 years and thyroid function in early childhood: a prospective cohort study Hwa Young Kim Received Received
  P1-432 LEVOTHYROXINE EFFECT ON THYROID VOLUME IN CHILDREN WITH AUTOIMMUNE HASHIMOTO THYROIDITIS (AHT) PRESENTING SUBCLINICAL (SH) OR OVERT (OH) HYPOTHYROIDISM Sofia Leka Received Received
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EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

58th Annual ESPE Meeting

 

19-21 September 2019 Viena
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    ACTIVE FROM 19/09/2019 TO 19/09/2020
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                   DOI: 10.3252/pso.eu.58ESPE.2019 
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   Poster submission deadline 17/09/2019
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