PosterSessionOnline

EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

58th Annual ESPE Meeting

19-21 September 2019 Viena

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

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

RFC10-001	Contemporary surgical approach in CAH 46XX Results from the I-DSD/I-CAH Registries	Alexander Springer	Received

P2-001	Gender identity, sexual orientation and quality of life in women with non-classic congenital adrenal hyperplasia	Anat Segev-Becker	Received

RFC7-001	Accuracy of glucose sensor estimate of HbA1c in children with type 1 diabetes	Sarah Ehtisham	Received

RFC8-001	Trade-off between Olfactory Bulb and Eyeball Volume in Precocious Puberty	murat karao&287;lan	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

T-001	Circulating miR-451a: a biomarker to guide diagnosis and treatment of polycystic ovary syndrome in adolescent girls	Marta Díaz	Received

RFC6-001	EFTUD2 gene deficiency disturbs maturation of osteoblast and inhibits chondrocyte differentiation via activated p53 signaling	Jing Wu	Received

RFC9-001	Targeted next-generation sequencing for congenital hypothyroidism with positive neonatal TSH screening results	Takeshi Yamaguchi	Received

RFC12-001	Ovarian follicles of young patients with Turner Syndromecontain normal oocytes but monosomic 45,X granulosa cells	Sapthami Nadesapillai	Received

P3-001	A case of Cushing syndrome in a Wilms tumour	Yvonne Lim	Received

RFC5-001	HURTHLE CELL CARCINOMA IN CHILDHOOD: RETROSPECTIVE ANALYSIS OF A LARGE SERIES	Giorgia Pepe	Received

RFC14-001	Papp-a2 deficiency results in sex-dependent modifications in hypothalamic regulation of energy homeostasis.	Jesús Argente	Received

P1-001	Could a Glucocorticoid Receptor Polymorphism be Protective against Hypothalamic-Pituitary-Adrenal Axis Suppression in Asthmatic Children on Corticosteroids?	Ekkehard Zllner	Received

RFC1-001	Low prevalence of maternal microchimerism in Japanese children with type 1 diabetes	Kikumi Ushijima	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

RFC4-002	Circulating Exosomal miRNAs profiles of Childrens Nonalcoholic Steatohepatitis	Xuelian Zhou	Received

RFC10-002	Cryptorchid boys with abrogated mini-puberty display differentially expressed genes involved in sudden infant death syndrome.	Faruk Hadziselimovic	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

RFC2-002	Does the treatment with recombinant human growth hormone improve final height in patients affected by X-linked hypophosphatemia?	JULIA ANDRE	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

P1-002	Software-assisted Analysis of the urinary Steroid Metabolom in treated children with classic Congenital Adrenal Hyperplasia	Clemens Kamrath	Received

P3-002	A rare cause of primer adrenal insufficiency: NROB1 (DAX1) mutation	Ozge Koprulu	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

RFC11-002	Prevalence and predicting factors of endocrine dysfunction in children with NF1 and optic gliomas.	Anna Grandone	Received

RFC15-002	BMP4 mutations as a novel cause of normosmic hypogonadotropic hypogonadism	A. Kemal TOPALOGLU	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

RFC5-002	Ultrasound features of multinodular goiter in DICER1 syndrome	Marek Niedziela	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

RFC13-002	Development of novel non-invasive strategies for monitoring of treatment control in patients with congenital adrenal hyperplasia	Irina Bacila	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

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

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

RFC11-003	Polycystic Ovarian Syndrome in Adolescents: Discovery Proteomics and the Search for Novel Non-Invasive Biomarkers	Harriet Gunn	Received

RFC2-003	Growth hormone effects on metacarpal bone geometry and bone age in growth hormone-deficient children	Daniel Zaldumbide	Received

P1-003	Simplifying the interpretation of steroid metabolome data by a machine-learning approach	tarik kirkgoz	Received

RFC10-003	Level of Uncertainty in Diagnostic Evaluation of Boys With XY Disorders of Sex Development (DSD)	Malika Alimussina	Received

P3-003	A 46, XX patient with 21-OHD diagnosed during the etiologic workup of male infertility.	TULAY TULAY	Received

RFC12-003	Imprinting defects and copy number variations in short children born small for gestational age	Masayo Kagami	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

T-003	Hypothalamus and Pituitary Gland Antibodies in Childhood-Onset Brain Tumors and Pituitary Dysfunction	GIUSEPPA PATTI	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

RFC7-003	Osteopontin as an Early Urinary Marker of Diabetic Nephropathy in Adolescents with Type 1 Diabetes Mellitus	Amany Ibrahim	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

RFC5-003	Experience of thyroid surgery in children with intraoperative neuromonitoring.	Alexander Anikiev	Received

RFC6-003	Increased burden of common risk alleles in children with a significant fracture history.	Despoina Manousaki	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

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

RFC4-004	The novel phosphatidylinositol-3-kinase (PI3K) inhibitor alpelisib effectively inhibits growth of PTEN haploinsufficient lipoma cells.	Anna Kirstein	Received

RFC5-004	Thyroid dysfunction in patients following thymus transplantation in a tertiary centre: a 10-year experience.	Sommayya Aftab	Received

P1-004	The Steroidal Milieu in Amniotic Fluid of Mid-Gestation: A Targeted GC-MS Metabolomics Study	Rong Wang	Received

RFC3-004	Peripheral glucocorticoid metabolim may reflect resolution of inflammation in Kawasaki disease	Shuji Sai	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

RFC13-004	Loss-of-function NNT mutations impair antioxidants mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficieny	Aline Faccioli Bodoni	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

RFC1-004	ESTIMATION OF MODY FREQUENCY AND PREVALENT SUBTYPES IN PEDIATRIC PATIENTS BY TARGETED NGS	Luis Salamanca	Received

P2-004	Bone age advancement in prepubertal children with premature adrenarche	Rita Santos-Silva	Received

RFC8-004	Evaluation of puberty in patients with Noonan syndrome and mutations in the RAS/MAPK genes.	Alexsandra Malaquias	Received

RFC2-004	Bone Mass and Fracture Prevalence in Childhood Brain Cancer Survivors 2, 5 or 7 years after off therapy	Annalisa Gallizia	Received

RFC10-004	qPCR screening for Xp21.2 copy number variations in patients with elusive aetiology of 46,XY DSD	Jakob Meinel	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

P3-004	A female infant with severe salt-wasting due to aldosterone synthase deficiency, initially mimicking adrenal insufficiency	Simone Krull	Received

RFC9-004	Correlation between Genotype and Phenotype characteristics in Children with Congenital Hyperinsulinism (CHI) in a specialist centre.	Laura Bosch i Ara	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

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

RFC14-004	GHR transcript heterogeneity may explain the phenotypic variability in patients with homozygous GHR pseudoexon mutation	Sumana Chatterjee	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

RFC4-005	GDF5 Promotes White Adipose Tissue Thermogenesis via p38 MAPK Signaling Pathway	Feihong Luo	Received

RFC1-005	Decreased circulating levels of MOTS-c in individuals with newly diagnosed type 1 diabetes children	Caiqi Du	Received

P2-005	Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency.	Asmar Aghayeva	Received

RFC5-005	A novel mutation in the Thyroglobulin gene leading to Neonatal goiter and Congenital Hypothyroidism in an Eritrean infant	Eve Stern	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

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

RFC7-005	Dual diagnosis of type 1 diabetes and ADHD	Kineret Mazor-Aronovitch	Received

RFC8-005	CHD7 mutations in patients with anosmic or normosmic idiopathic hypogonadotropic hypogonadism.	Leman Damla KOTAN	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

RFC13-005	Genetics of Familial Glucocorticoid Deficiency over the Decades: Phenotypic Variability and Associated Features	Chris Smith	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

RFC12-005	Cognitive and Neuroradiological assessments in Silver Russell patients	GIUSEPPA PATTI	Received

P3-005	Can early prenatal prednisone treatment reduce virilization of CAH female newborn?	Alessandra Sauna	Received

RFC9-005	Spectrum of Neuro-developmental disorders in Children with Congenital Hyperinsulinism due to activating mutations in GLUD1.	Sommayya Aftab	Received

RFC10-005	Variants in NWD1 gene leading to different degrees of gonadal dysgenesis	Odile Christin Gaisl	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

RFC8-006	Growth, pubertal course and long-term outcome of 46,XY boys born with atypical genitalia and low birthweight	Lloyd Tack	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

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

RFC3-006	Prevalence of endocrine complications in Duchenne muscular dystrophy	Primo Kotnik	Received

RFC10-006	A mutation in the nucleoporin-107 gene causes aberrant Dpp/BMP signaling and XX gonadal dysgenesis	Tikva Shore	Received

P2-006	CORTICOSTEROID USE: PRACTICES AND ATTITUDES OF PEDIATRICIANS	Yael Lebenthal	Received

T-006	Obesity in pediatric age: the analysis of genomic rearrangements	Simona Filomena Madeo	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

RFC14-006	GrowthHormone Deficiency (GHD): Assessing Burdenof Disease in Children and Adolescents: the Growth Hormone Deficiency ChildImpact Measure (GHD-CIM)	Meryl Brod	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

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

RFC4-006	Appetite Suppressing Effects of Glucoregulatory Peptides Devoid of Nausea	Christian Roth	Received

RFC13-006	Inhibitory effects of Curcuma longa extract on the steroid metabolizing cytochrome P450 enzymes	Patricia Rodríguez Castaño	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

P2-007	Updates on genotype and phenotype of Vietnamese Patients with X-Linked Adrenoleukodystrophy	THU HA NGUYEN	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

P3-007	Rare case of cortisol producing tumour in 14 years old girl.	Helena Grskog	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

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

P2-008	NOVEL TBX19 MUTATION AS CAUSE OF HYPOGLICEMIA IN TWO SIBLINGS	Andrea Castagna	Received

T-008	Bone mineral density (BMD) in women with Turner syndrome (TS) from the DSD-LIFE cohort, an epidemiological study	Audrey Cartault	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

P1-008	Follow-up and Prevalence of Precocious Puberty in Children with Classical Congenital Adrenal Hyperplasia diagnosed by Neonatal Screening	Veronica Gonzalez	Received

LB-009	Left ventricular mass index and cardiovascular function in adolescents born small for gestational age (SGA)	Indre Petraitiene	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

P2-009	The clinical polymorphism and variability of X-linked adrenoleukodystrophy in one Russian family.	Leila Sozaeva	Received

P3-009	Late onset 11 Beta Hydroxylase Deficiency: Two cases	Elvan Bayramoglu	Received

T-009	Empagliflozin And GABA Improve &946;-Cell Mass And Glucose Tolerance In Streptozotocin-Treated Mice	Sophie Welsch	Received

P3-010	An unusual Testicular Adrenal Rest Tumor localization in a 15-year-old boy with congenital adrenal hyperplasia.	Domenico Corica	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

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

P2-010	Functional adrenocortical oncocytoma a rare cause of progressive virilization and secondary amenorrhea	Katja Dumic Kubat	Received

P1-011	ASSESSMENT OF THE ADRENAL FUNCTION IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA BEFORE AND AFTER INDUCTION THERAPY WITH CORTICOSTEROIDS	doaa khater	Received

LB-011	Height in Inborn Errors of Metabolism requiring hypoprotidic diet: a longitudinal follow up study about 213 patients	kanetee Busiah	Received

P3-011	Primary Adrenal insufficiency in Sudanese children (clinical presentation, etiology and diagnostic challenges)	Salwa Elhassan	Received

T-011	Droplet Digital PCR Techniques to detect R201 mutations in the Mccune-Albright Syndrome	wenli Lu	Received

P2-011	Long-term Prednisone versus Hydrocortisone Treatment in Children with Classic Congenital Adrenal Hyperplasia (CAH): A Controlled Study	Shayma Elsayed	Received

P2-012	A case of X-linked adrenoleukodystrophy presenting with primary adrenal insufficiency and normal VLCFA	Beyhan zkaya	Received

P1-012	Trientine treatment mimicking severe hyperandrogenism	Gerhard Binder	Received

T-012	The first description of large pathogenic deletion in ACAN gene and additional cases with novel pathogenic ACAN variants	Lana Stavber	Received

P3-012	Clinical follow-up of a novel NR0B1 mutation in a case of Adrenal Hypoplasia Congenital??	Haihua Yang	Received

LB-012	Thyroid function in neonates conceived after hysterosalpingography with iodinated contrast media	Nienke van Welie	Received

LB-013	Gut hormones secretion across clusters of Metabolic Syndrome in obese prepubertal children	Nella Polidori	Received

T-013	Results from the implementation of a 2 year growth awareness and growth disorders screening campaign (GrowInform)	Kaloyan Tsochev	Received

P1-013	Cytokines and the impairment of puberty	Natalia Shlyachova	Received

P3-013	Genotype and phenotype, growth outcome in 33 Korean patients with 21-hydroxylase deficiency	Ju Young Yoon	Received

P2-013	Different Potent Glucocorticoids, Different Routes of Exposure but The Same Result: Iatrogenic Cushings syndrome and Adrenal Insufficiency	Ayla Guven	Received

LB-014	Prenatal smoke-exposure is associated with increased anogenital distance in female infants	Deniz zalp Kizilay	Received

P3-014	One case report of Uighur girl with Cushing syndrome	wenjing li	Received

P2-014	Differences between normal-BMI girls with Premature Adrenarche and overweight or obese girls with Premature Adrenarche	Rita Santos-Silva	Received

T-014	The Effect of Endocine Disrupting Chemicals to Precocious Puberty in Children with Exposure History of Slim	Jung Eun Moon	Received

P1-014	Refractory hypercalcemia after Denosumab treatment in pediatric age: a case report	annalisa deodati	Received

T-015	Intestinal microbiota development differs between pubertal boys and girls	Sampo Kallio	Received

P1-015	The overweight and obesity decrease the growth potential in Mexican children and adolescents.	América Liliana Miranda - Lora	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

P3-015	Nephrotic Syndrome Developed in a Girl With Lipoid Adrenal Hyperplasia due to StAR gene mutation First Report	Kyung Mi Jang	Received

P2-015	Rare Causes of Primary Adrenal Insufficiency at King Faisal Specialist Hospital -Retrospective Study	Mohammed Alotaibi	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

P3-016	Pneumocystis Jiroveci pneumonitis complicating neonatal Cushings syndrome - the therapeutic dilemma	Adi Auerbach	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

P1-016	Normocalcemic Hyperparathyroidism in Children	DIMITRIOS PAPADIMITRIOU	Received

P3-017	Newborn screening for congenital adrenal hyperplasia: should we worry more about false positives or false negatives?	Sara Ciccone	Received

P2-017	Duodenal web presenting as pseuhypoaldosteronism in infancy.	Mireille El Bejjani	Received

T-017	FACTORS ASSOCIATED WITH DYSLIPIDEMIA IN PATIENTS WITH TYPE 1 DIABETES: A SINGLE-CENTER EXPERIENCE	Sari Krepel Volsky	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

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

LB-018	Exploratory case-control study on ACE2 expression in children with short stature	Gianluca Tornese	Received

T-018	Early treatment with intravenous bisphosphonates prevents severe postnatal bone loss in children with Osteogenesis imperfecta	Mirko Rehberg	Received

P1-018	Nephrocalcinosis in children with X-Linked Hypophosphatemia: prevalence and risks factors	Mathilde Grapin	Received

P2-018	A rare case of pseudohypoaldosteronism in a neonate secondary to congenital hydrometrocolpos	Shruti Kumar	Received

P3-018	The unusual adverse side effects of super-potent topical steroids.	Yasmine Abdelmeguid	Received

LB-019	CDX2 polymorphism of VDR gene and lipid profile in patients treated for acute lymphoblastic leukemia during childhood.	Ewa Barg	Received

P2-019	Hyperandrogenism in a 13-year-old girl due to glucocorticoid receptor mutation	Osnat Admoni	Received

T-019	Urinary Gonadotrophins in Girls with Turner Syndrome	Alessandra Boncompagni	Received

P3-019	A case with central adrenal insufficiency and early onset obesity: Proopiomelanocortin deficiency	Sezer Acar	Received

P1-020	Long-term Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism	Raffaele Buganza	Received

P3-020	Short Synacthen Test in Children at Sultan Qaboos University Hospital; Reviewing the sampling times	Hussain Alsaffar	Received

T-020	Molecular and phenotypicspectrum of Noonan syndrome in Chinese patients	Xin Li	Received

P2-020	Polydipsia, hyponatremia and a biochemical profile of aldosterone synthase deficiency	Christina Reinauer	Received

LB-020	Introduction of flash glucose monitoring in children with Type 1 diabetes: experience of a single-centre in Spain	Robert Brines	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

P3-021	Pheochromocytoma in children: a case report	Thanh Nguyen Trong	Received

P2-021	Fludrocortisone treatment in a child with Postural Orthostatic Tachycardia Syndrome (POTS): a case report.	Gaia Varriale	Received

P3-022	A Case with Congenital Adrenal Hyperplasia Diagnosed by Malnutrition	emine demet akba&351;	Received

LB-022	TWO NOVEL MUTATIONS OF THE LHX3 GENE ASSOCIATED WITH A SEVERE PHENOTYPE INVOLVING ENDOCRINE, NERVOUS AND SKELETAL SYSTEMS	LAURA GUAZZAROTTI	Received

P1-022	Differences in bone strength and cortical bone parameters in young Swedish women with Type 1 diabetes	Eva Kristiansen	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

P3-023	Recurrent Hypoglycemia-Not every low sugar is hyperinsulinemia	DEEPTI CHATURVEDI	Received

P1-023	INCREASED PREVALENCE OF OVERWEIGHT AND OBESITY AND ITS CLINICAL PREDICTORS IN CHILDREN AFFECTED BY X-LINKED HYPOPHOSPHATEMIA	VOLHA ZHUKOUSKAYA	Received

P2-023	Girls with idiopathic premature adrenarche achieve normal adult height.	Leandro Soriano-Guillén	Received

LB-024	Abdominal adiposity and total body fat as predictors of cardiometabolic health in pre-pubertal and pubertal youth	BInghan Jin	Received

P2-024	Adult height and growth pattern in patients with classic congenital adrenal hyperplasia	Ga Hyun Lee	Received

P1-024	Novel Homozygous LRP5 Mutations in Patients with Osteoporosis-Pseudoglioma Syndrome	Fatemeh Saffari	Received

P3-025	Unusual association : Allgrove syndrome and hypopituitarism	Mouna Mnif Feki	Received

LB-025	Low Trabecular Bone Score in Children with Inflammatory Bowel diseases	Yael Levy Shraga	Received

P2-025	Cushing Syndrome due to an adrenacortical carcinoma in a baby with atypical Beckwith-Wiedemann Syndrome	eltan mehmet	Received

P1-025	Pathogenicity of GCK gene mutation c.364CG (p.Leu122Val)	David Crudo	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

P1-026	Myocardial function in asymptomatic children with type 1 diabetes	hager barakizou	Received

LB-026	Dramatic clinical response to Lenvatinib in one pediatric patient with advanced metastatic papillary thyroid carcinoma	Noelia Dujovne	Received

P3-026	Title: Long-term outcome of congenital adrenal hyperplasia patients at KFSHRC-Saudi Arabia. Tertiary Center Experience	Haneen Aldalaan	Received

P3-027	A boy with adrenal hypoplasia congenita without external genital abnormalities	Ikumi Umeki	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

P2-027	The First Case Report of SEMD-JL1 in China	ke Huang	Received

P1-027	A Case of Neonatal Diabetes with Hyperferritinemia: A Distal PTF1A Enhancer Mutation	Glin Arslan	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

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

LB-028	The Volumetric Changes in the Olfactory Bulb Depend on Body Mass Index	murat karao&287;lan	Received

P1-029	What hypoglycemia does to the heart: Impact of nocturnal hypoglycemia on cardiac repolarization in diabetic children.	Sara Bachmann	Received

P2-029	Clinical and Genetic Characteristics of Pseudohypoparathyroidism Type 1A in Children Based on Single-center Cohort Study	Xuelian Zhou	Received

P3-030	ENPP1 hypophosphatemic rickets in a 3.6 years old Italian child	Daniele Tessaris	Received

P1-030	Effects of Glypican-4 Protein on INS1E Cell Viability and Insulin Signaling	Joseph Buhl	Received

P2-030	A rare case of neonatal hypocalciuric hypercalcemia complicated with arrhythmia	Yuto Arai	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

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

P2-032	Pediatric patients with heterozygous ALPL mutation show a broad clinical phenotype	Corinna Melanie Brichta	Received

P1-032	Heterozygous RFX6 mutation as a cause of diabetes mellitus in a multigenerational family	Nehama Zuckerman Levin	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

P3-033	In case of osteogenesis imperfecta transmission in pregnancy: check vitamine D and calcium status of the mother.	Valerie PORQUET-BORDES	Received

P2-034	Chronic Bone Disease in Pediatric Sickle Cell Disease Including a Case of Successful Bisphosphonate Therapy	Chelsey Grimbly	Received

P1-034	Serum Dipeptidyl peptidase-4 Activity and its Relation to Insulin Resistance in Type 1 Diabetic Adolescents	Amany Ibrahim	Received

P1-035	The impact of CGM availability: real world data from a population based clinic	Elaine Sanderson	Received

P3-035	Pseudohypoparathyroidism: Four cases reports	Marina Bressiani	Received

P2-035	Clinical and genetic characteristics of 168 Russian patients with hypophosphatemic rickets	Kristina Kulikova	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

P2-036	A 10-year-old girl with primary hypoparathyroidism and systemic lupus erythematosus (SLE)	Hanna Borysewicz-Sa&324;czyk	Received

P3-036	A Case of Robinow syndrome	Huseyin Anil Korkmaz	Received

P2-037	An unusual case of hyperparathyroidism: familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) associated with mutations in CLDN19	Yuezhen Lin	Received

P1-037	Association of maternal depressive symptoms with worse metabolic control in adolescents with Type 1 Diabetes	Hernan Garcia-Bruce	Received

P1-038	The factors associated with high levels of HbA1C in children and young people with Type 1 Diabetes mellitus	Omolola Ayoola	Received

P3-038	Mild Hypophosphatasia in a Family with a Novel Mutation in the ALPL gene	YONG HEE HONG	Received

P2-038	Skeletal Maturity and Growth in children with Type 1 diabetes	Nikhil Lohiya	Received

P2-039	Bone mineral status in adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency	imen gargouri	Received

P1-039	Differences between short- and long-term outcomes of laparoscopic sleeve gastrectomy in adolescence	Marina Ybarra	Received

P3-039	UNCOMMON ASSOCIATION OF HYPOPARATHYROIDISM AND RENDU-OSLER SYNDROME	MIRELA IANCU	Received

P3-040	Barakat Syndrome (HDR Syndrome): Case Report	Marina Bressiani	Received

P2-040	REDUCED BONE MINERAL DENSITY IN CHILDREN WITH INFLAMMATORY BOWEL DISEASE WITHOUT EXPOSURE TO CORTICOSTEROID TREATMENT	Feneli Karachaliou	Received

P2-041	A clinical dilemma in the detection of paediatric hypophosphataemia	Clement Ho	Received

P1-041	Growth arrest-specific 6 (Gas6) protein is associated with adiposity and metabolic syndrome in obese children and adolescents	Daniel Zaldumbide	Received

P3-041	Myelofibrosis in Severe Vitamin D Deficiency Rickets: A Case Report	Omar Magdy Omar	Received

P3-042	Congenital Hyperinsulinism in Kosova	Vjosa Mulliqi Kotori	Received

P3-043	About a case of neonatal hypocalcemia	Gilda Belli	Received

P1-043	Association of biomarkers of endothelial dysfunction with MicroRNAs levels in overweight and obese adolescentes	Fengyang Huang	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

P2-044	Cinacalcet experience in hypercalcemia due to CaSR mutation	Esra Dger	Received

P3-045	Acute Lymphoblastic Leukemia;Atypically Presenting with Sever Hypercalcemia in a Palestinian Child	HASAN EIDEH	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

P2-045	Two siblings with hypophosphatemic rickets: SLC34A3 gene mutations with different clinical phenotypes	Esin Karakilic Ozturan	Received

P2-046	Seasonal 25-hydroxy Vitamin D3 variations in school-aged children from Santiago de Chile	Helena Poggi	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

P1-048	Waist circumference triglyceride index is useful to predict non-alcoholic fatty liver disease in childhood obesity.	Bahar zcab&305;	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

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

P2-049	Successful treatment with enzyme replacement therapy in a girl with severe infantile Hypophosphatasia	Katrin Heldt	Received

P1-049	Gut Microbiome of North-American Children with and without Prader-Willi Syndrome (PWS)	Andrea Haqq	Received

P3-050	Hybrid diabetes with good response to metformin in an Adolescent with polyglandular polyendocrinopathy (APS2)	noor Hamed	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

P1-051	Pathogenic mutations and variants in KSR2 in a cohort of obese children	Ingrid Krber	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

P3-052	Off label use of CGM in a pediatric patient with type 1 Diabetes Mellitus under the age of 2	Liliana Burdea	Received

P1-052	EFFECT OF FEEDING MODE ON LONGITUDINAL BODY COMPOSITION IN EARLY LIFE	Kirsten de Fluiter	Received

P2-052	A rare cause of hypophosphatemia: Raine Syndrome	mehmet eltan	Received

P3-053	A case of congenital hyperinsulinism due to ABCC8 mutation: A challenge to diagnosis, management, and treatment	Zacharoula Karabouta	Received

P2-053	Idiopathic infantile hypercalcemia: Mutations in SLC34A1 and CYP24A1 in two siblings and fathers	Ayla Guven	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

P1-054	Augmented Fibroblast Growth Factor 21 Serum Levels in Metabolic Disorders and Association With Endothelial Function in Childhood	Eleni Domouzoglou	Received

P3-054	Relationship between Chloride infusion and Base Excess in initial treatment of pediatric diabetic ketoacidosis	Kentaro Sawano	Received

P1-055	A novel recurrent heterozygous PLIN1 mutation in three Russian patients with partial lipodystrophy, dyslipidemia and insulin resistance.	Yulia Tikhonovich	Received

P2-055	A novel missense COL10A1mutation identified by next generation sequencing in a Chinese pedigreewith Schmid metaphyseal chondrodysplasia	Qiong Chen	Received

P3-055	The role of patient adherence to insulin pump therapy with long-term treatment of type 1 diabetes	Mariia Turkunova	Received

P2-056	a case report of a girl with short stature has laron syndrome and spondyloepimetaphyseal dysplasia	Abdullah Alshahrany	Received

P3-056	Long-term honeymoon period in Type 1 diabetes: True diagnosis MODY5; New mutation of HNF1B	Esra Dger	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

P2-057	A NOVEL MUTATION OF PHEX GENE INDUCING X-LINKED HYPOPHOSPHATEMIA RICKETS, A CASE REPORT	RENATA PINTO	Received

P3-057	Prevalence of Celiac disease (CD) and autoimmune thyroid dysfunction (AITD) in Indian children with Type 1 Diabetes	Vasundhara Chugh	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

P2-058	Skeleton muscles and tissues metabolic activity in Greek adolescent PCOS	Styliani Geronikolou	Received

P1-058	A case-control study of exposure to bisphenol-A and phthalates in obese children	annalisa deodati	Received

P2-059	SPONDYLOOCULAR SYNDROME: PRESENTATION OF TWO SIBLINGS DIAGNOSED WITH THE RARE DISEASE AND THE RESULTS OF PAMIDRONATE THERAPY	Yagmur Unsal	Received

P1-059	Growth patterns in non-syndromic childhood overweight: comparing children with early of late onset weight gain	Alina German	Received

P2-060	Clinical and Genetic Characterization of Tunisian Children with Hereditary Hypophosphatemic rickets (HHR).	Selmen Wannes	Received

P2-061	Osteogenesis Imperfecta: Genetic evaluation	Lidia Castro-Feijoo	Received

P3-061	The Effect of Fibroblast Growth Factor 23 on Serum Phosphorus Level in Children with Diabetic Ketoacidosis	Hakan Doneray	Received

P2-062	The Effect of Carbohydrate Recognition and Counting Ability on Glycemic Control in Pediatric Patients with Type 1 Diabetes	Minutti Carla	Received

P3-062	What does the insulin pump change in children with type 1 diabetes? One-year clinical follow-up	Ilknur Arslanoglu	Received

P3-063	Severe heart disease can cause diabetes mellitus even in younger age: Case reports of two Japanese adolescent boys.	Yukie Izumita	Received

P1-063	Altered gut microbiota in Obese children: sex-associated signature	Ruimin Chen	Received

P2-063	A Rare Case of Syndromic Diabetes due to an INSR pathogenic variant	Tara Tayeb	Received

P1-064	Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome.	Louise Sonia	Received

P2-064	Autoimmune thyroid diseases in children and adolescents with Maturity Onset Diabetes of the Young	Valeria Calcaterra	Received

P3-064	De novo mutation of ABCC8 gene in a child with MODY developed at 25 months of age	Jeesuk Yu	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

P3-065	Insulin-induced oedema in a child with newly diagnosed diabetes mellitus	Meltem Didem cakir	Received

P1-066	Salivary free cortisol measurement: A diagnostic Approach to assess adrenal failure in symptomativ premature patients	Felix Reschke	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

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

P1-067	Screening of congenital hypothyroidism using umbilical cord blood in a maternity hospital	Clement Ho	Received

P3-068	Seasonal variation and epidemiological parameters in children from Western Greece with Type 1 Diabetes Mellitus (T1DM).	Eirini Kostopoulou	Received

P2-068	Pancreatic Cell Function and its relationship with iron overload in Patients with -Thalassemia Major	Lina ZHANG	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

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

P2-070	Evaluation of -cell function in young MODY patients using a Mixed Meal Tolerance Test	Ingrida Stankute	Received

P3-070	Indicators of Caries Risk in Children with Type 1 Diabetes Mellitus	Ehsan Mowafy	Received

P1-070	Congenital Hypothyroidism Precise Diagnosis with Dual Imaging	ramona nicolescu	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

P2-071	The Effect of Different Forms of Maternal Dysglycemia on the occurrence of Neonatal Hypoglycemia in babies admitted to NICU.	Ashraf Soliman	Received

P1-071	Clinical, biochemical and echocardiographic evaluation of patients with congenital rickets due to maternal vitamin D deficiency	Huseyin Demirbilek	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

P3-072	Hematologic indices indicating platelets activity in children with type 1 diabetes	setila dalili	Received

P2-072	ADROPIN, AFAMIN AND NEUDESIN - NOVEL BIOMARKERS OF TYPE 1 DIABETES MELLITUS IN CHILDREN	Agnieszka Polkowska	Received

P2-073	Prevalence, Time trend and predictors of Celiac Disease in Type 1 Diabetes	neha agarwal	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

P3-073	THE PREVALENCE OF HYPERTENSION AND ITS RELATIONSHIP TO GLYCEMIC CONTROL IN CHILDREN WITH TYPE 1 DIABETES MELLITUS	doaa khater	Received

P3-074	Does metformin therapy prolong the honeymoon period in obese adolescent with hybrid diabetes?	Noor Hamed	Received

P1-074	RECOMBINANT GH TREATMENT IN CHILD WITH PSEUDOPSEUDOHYPOPARATHYROIDISM ASSOCIATED WITH GROWTH HORMONE DEFICIENCY	Feneli Karachaliou	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

P2-075	Impact of Insulin treatment of Cystic Fibrosis Related Diabetes (CFRD) on BMI and respiratory function	Manuela Caruso-Nicoletti	Received

P1-075	Impact of -202 IGFBP-3 Promoter Polymorphism on Growth Responses in Korean Children with Idiopathic Short Stature	Seung Yang	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

P2-076	Coexistence of Medium chain acyl-CoA dehydrogenase deficiency (MCADD) and Type 1 diabetes (T1D): A management challenge	Donald Afreh-Mensah	Received

P3-076	Extra attention to be paid when looking after boys with Type 1 Diabetes Mellitus in Oman	Hussain Alsaffar	Received

P3-077	Factors affecting the preservation of C-Peptide Secretion in Egyptian children with Type 1 Diabetes	Amany El-hawary	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

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

P2-078	A case of an infant with congenital hyperinsulinism complicated by diabetic ketoacidosis during treatment	CHAERI YOO	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

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

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

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

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

P3-082	Assessment of testicular volume by Ultrasound in Children and Adolescents with Type 1 diabetes	Nikhil Lohiya	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

P2-082	Thiamine responsive megaloblastic anemia syndrome with restrictive cardiomyopathy: a case report	Wafaa Laymoun	Received

P2-083	17q12 Deletion and a Family History of Diabetes	ramona nicolescu	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

P1-083	Identification of novel recessive IGFALS mutations and INSR variant in an obese Korean boy	Yoo-Mi Kim	Received

P1-084	Development of a parent experience measure forparents of children with achondroplasia	Jane Beck	Received

P3-084	A low-carbohydrate diet improves metabolic control in a type 1 diabetic child without side effects	Philippe Klee	Received

P2-084	An Unusual Presentation of Type 1 Diabetes	faisal alwadiy	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

P2-085	Clinical characteristics and treatment outcomes in patients with autoantibody-negative ketosis-prone diabetes	Shin-Hee Kim Kim	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

P2-086	Factors influencing the formation and support of the motivation to self-control of adolescents with type I diabetes mellitus	Olena Kyrylova	Received

P1-086	Extreme short stature and poor pubertal growth: when FBN1 is the culprit	Cécile Brachet	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

P2-087	Glycemic Control in Egyptian Adolescent Girls with Type 1 DM	yomna shaalan	Received

P3-088	A case of Type 2 diabetic adolescent with sleep apnea who was successfully stopped metformin after adenotonsillectomy	Ji-Young Seo	Received

P2-088	A qualitative study investigating the experiences of using Solution Focused Therapy in a paediatrics diabetes team.	Mark Guyers	Received

P1-088	Etiology of Severe Short Stature: Single Center Experience	Matti Hero	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

P3-089	A mitophagic response to iron overload-induced oxidative damage associated with the PINK1/Parkin pathway in pancreatic beta cells	Lina ZHANG	Received

P2-090	NEONATAL DIABETES IN TWO SIBLINGS WITH FOXP3 VARIANT	MARIA CAROLINA COLOMBI GONZALEZ	Received

P3-091	Association of type 1 diabetes and celiac disease in child	Daniel Zaldumbide	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

P2-091	A novel variant of the WFS1 gene with dominant inheritance causing Wolfram-like syndrome	Juraj Stanik	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

P1-092	A rare case of pseudoisodicentric X chromosome in a patient with primary amenorrhoea	Saskia Schipper	Received

P3-092	Case of family neonatal diabetes with KCNJ11 gene mutation: dynamics monitoring	Svitlana Chumak	Received

P2-093	The growth hormone treatment and carbohydrate metabolism in children born small for gestational age.	Dominika Labochka	Received

P1-093	Persisting Embryonal Infundibular Recess in a patient with Morning Glory Syndrome and multiple pituitary deficiencies	ADALGISA FESTA	Received

P1-094	Familial occurrence of Turner syndrome in two Tunisian families	imen gargouri	Received

P2-094	Empirical sulphonyurea in Neonatal diabetes: results from a aTertiary care centre	smita ramachandran	Received

P3-095	Changes in the Microbiome of Pre-Type 1 Diabetic Children	Nikolina Zhelyazkova	Received

P2-095	Diabetes Mellitus, Severe Acanthosis Nigricans and Short Stature: a Rare Association in Chinese Children	Miaoying Zhang	Received

P1-095	The role of physical activity on postural stability and fitness characteristics in pediatric patients with GH deficiency	Maria Cristina Maggio	Received

P3-096	Assessment of cardiac function in obese children and adolescents with metabolic syndrome	Penio Kassari	Received

P2-096	Evaluation of celiac disease antibodies and 25-OH vitamin D in type 1 diabetic patients	Lusine Navasardyan	Received

P1-096	Assessment of subjective and objective compliance to growth hormone therapy of children with growth hormone deficiency	Elpis Athina Vlachopapadopoulou	Received

P3-097	Metabolic Syndrome in adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency	imen gargouri	Received

P1-097	Familial Neurohypophyseal Diabetes Insipidus and 2 Novel Vasopressin Gene Mutations in 13 Italian Kindreds.	GIUSEPPA PATTI	Received

P2-097	Does commencing on an insulin pump improve glycaemic control in paediatric patients?	Nuthana Prathivadi Bhayankaram	Received

P3-098	High allostatic load in children with excess of weight	Valeria Calcaterra	Received

P1-098	Final height in oncological growth hormone deficient (GHD) children after growth hormone (GH) therapy	Giulia Rodari	Received

P2-098	Prevalence of Neonatal Macrosomia (NM) and Its Relation to Hypoglycaemia (NH) in Normoglycemic Versus Dysglycemic Pregnant Women.	Ashraf Soliman	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

P1-099	Eating Behavior and Oxytocin in Childhood-onset Craniopharyngioma Patients: An Exploratory Study	Hermann L. Muller	Received

P2-099	A Case of Neonatal Diabetes Due to Newly Defined Mutation in the GLIS 3 Gene	Yilmaz Kor	Received

P2-100	Hypertriglyceridemia as a complication of severe diabetic ketoacidosis in newly diagnosed diabetes - a case report.	Matylda Hennig	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

P3-100	An infant with severe hypertriglyceridemia: Acute and long-term management in the paediatric population	Sarah WY Poon	Received

P3-101	BigO: The use of new technologies for the management of childhood obesity A clinical pilot study	Penio Kassari	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

P1-101	Identification of novel mutations in FGFR1 and functional characteristics in patients with isolated gonadotropin-releasing hormone deficiency	Yena Lee	Received

P1-102	Clinical Presentation, Management, and the Outcomes of Pituitary Adenomas in children	aashish sethi	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

P3-102	Obesity and Insulin Resistance: Differences between pubertal and prepubertal children	Eirini Dikaiakou	Received

P1-103	A case of panhipopituitarism with SOX3 gene deletion	Esra Dger	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

P2-103	Evaluation of the association of glutamic acid decarboxylase antibody and limbic encephalitis in children with type 1 diabetes mellitus	Esra Dger	Received

P2-104	Insulin pump therapy implementation in Uzbekistan	Khilola Hanmehmet	Received

P1-104	Interesting Genotype-Phenotype Differences in Siblings with Familial Hypopituitarism and Pituitary Hypoplasia	Emma Thorley	Received

P3-104	Treating Paediatric Morbid Obesity using the Multidisciplinary Intensive Inpatient Approach	Ruma Deshpande	Received

P2-105	Cardiopulmonary exercise testing, body composition and metabolic status after allogeneic hematopoetic stem cell transplantation in childhood	Kathleen De Waele	Received

P1-105	Familial Central Precocious Puberty Caused by a Novel MKRN3 Mutation	Osnat Admoni	Received

P3-106	PHENOTYPIC AND GENOTYPIC PROPERTIES OF CHILDREN WITH SUSPICION OF MONOGENIC OBESITY	Hayrullah Manyas	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

P2-106	School-age children awareness of seriousness of obesity problem, health-related outcomes and effectiveness of self-control preventive strategies	Tetyana Chaychenko	Received

P2-107	Childhood Obesity and Iron Metabolism	Julia Galhardo	Received

P3-107	Relation of serum 25 hydroxy-vitamin levels D3 with body-mass index in pediatric patients	paula sol ventura wichner	Received

P3-108	VITAMIN B12 LEVELS IN CHILDREN AFTER METFORMIN TREATMENT	Kostova Yordanova	Received

P2-108	Effectiveness of Multidisciplinary Outpatient Approach in the Management of Paediatric Obesity	Ruma Deshpande	Received

P2-109	Metabolic syndrome in children and adolescents who survived after childhood cancer.	Anna Gavrilova	Received

P1-109	A NCOA5 gene variant in a pedigree with maternally inherited precocious puberty	Magdalena Avbelj Stefanija	Received

P3-109	Follow-up evaluation of clinical markers and inflammatory, biochemical and hormonal profiles in children with bodyweight problems	Ioana Taranu	Received

P2-110	Pubertal milestones and related hormonal changes among children with obesity	Robert Stein	Received

P1-110	Novel references for ultrasound estimated testicular volumes and pubic hair in 6-16 year-old Norwegian boys	Ninnie Oehme	Received

P3-110	Gastroduodenopathies in obese young people	Olena Tolstikova	Received

P1-111	PROKR2 in in girls with idiopathic central precocious puberty	Anna Grandone	Received

P3-111	Seven Methods of indicating childhood Metabolic Syndrome	shahin koohmanaee	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

P3-113	SEVERE HYPERNATREMIA REVEALING A ROHHAD-NET SYNDROME.	YASMINE OUAREZKI	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

P1-114	Obesity in boys is not associated with delayed pubertal onset	Alexander Busch	Received

P3-114	RARE CASE OF ACQUIRED GENERALIZED LIPODYSTROPHY IN A 14-YEAR OLD PATIENT	Dumitrescu Cristina Patricia	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

P3-115	Gender-based differences in the clustering of metabolic syndrome factors in children and adolescents.	Valeria Calcaterra	Received

P1-115	Mutation screening of the Sonic Hedgehog signaling-related genes in 120 Japanese patients with congenital hypopituitarism	Masaki Takagi	Received

P1-116	How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty	tarik kirkgoz	Received

P3-116	Fat mass index and fat-free mass index percentiles in healthy Spanish adolescents.	Teodoro Durá-Travé	Received

P2-116	Nonalcoholic Fatty Liver Disease in Pediatric Obese Patients	giorgiana brad	Received

P2-117	Trends in childhood obesity, underweight and short stature among urban school children in Romania	Raluca-Monica Pop	Received

P1-117	The Role of Rat Hypothalamus Kisspeptin, Neurokinin and their respective Receptors in the Prolactin-Infertility Interaction	Bertan Yilmaz	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

P3-118	Somatostatine Analogue in Hypothalamic Obesity	Belma Haliloglu	Received

P2-118	Impact of a comprehensive program, on prevalence of childhood obesity in Andalusia, Spain.	María Rocío Hernández-Soto	Received

P1-118	Whole Exome Sequencing (WES) reveals oligogenic gene mutations in a case of Combined Pituitary Hormone Deficiency (CPHD).	AMALIA SERTEDAKI	Received

P3-119	PHYSICAL ACTIVITY, FOOD AND METABOLIC RISK IN CHILDREN AND ADOLESCENTS	Carmela de Lamas	Received

P2-119	Evaluation of Fetuin-A level and related factors in obese adolescents	Glin Karacan Kucukali	Received

P1-119	Menarche and its relation to the pubertal growth spurt	Jenni Gardstedt	Received

P2-120	Prevalence of Obesity among Infants Presenting with Intussusception	Omar Magdy Omar	Received

P1-120	ROLE OF PRIMING IN PERI-PUBERTAL GROWTH DELAYS: PRELIMINARY RESULTS OF A LARGE MULTICENTER STUDY	Elena Galazzi	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

P3-121	Associations between lipid parameters and insulin resistance in obese adolescents	Tetyana Chaychenko	Received

P2-121	A non-invasive model for detection of the metabolic syndrome in children and adolescents	Junfen Fu	Received

P1-121	Lower urinary tract dysfunction and infection in girls with disorders of sex development and urogenital sinus	Alexander Anikiev	Received

P3-122	THE CHARACTERISTIC OF THYROID STATUS IN OVERWEIGHT AND OBESE YOUNG PEOPLE WITH INSULIN RESISTANCE	Olena Tolstikova	Received

P2-122	Insulin-like growth factor-1 and binding protein-3 in children with metabolic syndrome	yoonji Lee	Received

P3-123	Validity of non-high-density lipoprotein cholesterol for detecting dyslipidemia among Korean adolescents	Hyo-Kyoung Nam	Received

P2-123	Overweight, obesity and hypertension among adolescents the impact of immigration and a acculturation	Orit Hamiel	Received

P1-123	Does the internet provide accurate and valid health information regarding disorders of sex development?	Toby Candler	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

P3-124	EARLY ONSET MONOGENIC OBESITY: TWO CASES WITH HOMOZYGOUS MUTATION IN LEPR GENE	Ozlem Nalbantoglu	Received

P1-125	A Health-Related Quality of Life Tool for Parents of Young Children With Disorders of Sex Development	Salma Ali	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

P2-125	Clinical features and genetic analysis of childhood dyslipidemia	Chao chun Zou	Received

P1-126	Longitudinal Changes In External Masculinisation Scores In Boys With XY Disorder Of Sex Development (DSD)	Malika Alimussina	Received

P2-126	TRACKING BODY MASS INDEX AND FAT MASS PERCENTAGE FROM INFANCY INTO CHILDHOOD	Inge van Beijsterveldt	Received

P3-126	Metabolic risk assessment in obese children using Hypertriglyceridemic waist (HTGW) phenotype. Can it be a useful screening marker?	Eirini Dikaiakou	Received

P2-127	The bilirubin/triglycerides ratio predicts changes over time in glycated hemoglobin in prepubertal healthy children	Elsa Puerto-Carranza	Received

P1-127	Mutations in CBX2 associated with gonadal anomalies in 46,XY and 46,XX individuals	Ken McElreavey	Received

P3-128	Lipid and glucose profiles in obese Algerian children and adolescents	Soraya Kerkouche	Received

P1-128	The novel founder homozygous V225M mutation in the 17HSDB3 gene causes aberrant splicing and severe XY-DSD	Floris Levy-Khademi	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

P1-129	Molecular diagnosis of patients with 46,XY differences in sex development in a single tertiary center.	Natalia Perez Garrido	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

P3-129	The effect of anthropometric indices at birth on obesity characteristics in school-age children	Dmitriy Latyshev	Received

P3-130	Acanthosis nigricans as a presentation of severe insulin resistance in obese children.	Maria Krajewska	Received

P2-130	SEVERE OBESITY MUCH MORE THAN AN UNHEALTHY LIFESTYLE	Joana Matias	Received

P2-131	Serum 25-Hydroxyvitamin D Levels and Insulin Sensitivity Across Pubertal Stages in Obese Children	Somboon Wankanit	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

P3-132	Recurrent apnea in a boy suffering from congenital hyperinsulinism in the course of diazoxide treatment.	J&281;drzej Nowaczyk	Received

P2-132	ASSOCIATION BETWEEN TSH AND METABOLIC SYNDROME IN OBESE CHILDREN AND ADOLESCENTS	Chiara Guzzetti	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

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

P2-133	Primary hyperlipidemia in children: experience of 11 years from a referral center in Vietnam	Mai Do	Received

P2-134	TUMOR NECROSIS FACTOR ALPHA IN METABOLIC SYNDROME DEVELOPMENT IN CHILDREN	Iwona Be&324;-Skowronek	Received

P3-134	Persistant Hypoglycemia in Children: Hyperinsulinemia	gl direk	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

P2-135	First Familial Occurrence of Prader-Willi Syndrome in China: Two Cases and Family Studies	Yunqi Chao	Received

P2-136	Insulin resistance and impaired glucose tolerance in overweight/obese adolescents attending an obesity clinic in Belgium	Renate Zeevaert	Received

P1-136	Serum estradiol is associated with inhibin B in healthy 1-6 years old girls.	Niels Birkebaek	Received

P1-137	Brain MRI Findings in Girls with Central Precocious Puberty in Taiwan: one medical center experience	FU-SUNG LO	Received

P2-137	Clinical characteristics and response to growth hormone treatment in patients with Prader-Willi Syndrome	Aydilek ak&305;r	Received

P3-137	Case report: A neonate with prolonged hypoglycemia	Adele Bodieu Kenmegne Spse Chetcha	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

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

P1-139	Gonadal function of female patients with Noonan syndrome	Sophie Moniez	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

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

P1-140	Methylation status of X inactivation-escape genes in controls and females with X chromosome rearrangements	Sayaka Kawashima	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

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

P2-141	Metabolic syndrome risk assessment in Indian children and adolescents	Vasundhara Chugh	Received

P3-141	TREATMENT OUTCOME OF GROWTH HORMONE IN TURNER SYNDROME CHILDREN	Bui Phuong Thao	Received

P1-141	Diagnostic Value of Anti-Mullerian Hormone Level in Adolescent Females with Polycystic Ovary Syndrome	Shereen Abdelghaffar	Received

P2-142	Vitamin D status in obese children and its relationship with leptin and adiponectin	Mona Nourbakhsh	Received

P1-142	Disorders of sex development (DSD): Inconsistencies between clinical features and peripheral blood cultured karyotypes	Nursen Gurtunca	Received

P1-143	BIOTINE INTERFERENCE IN A PATIENT WITH NON-CLINIC HIGH THYROID HORMONE LEVELS	Hayrullah Manyas	Received

P2-143	Two Siblings with Tyrosinaemia Type 1 and Transient Hyperinsulinaemic Hypoglycaemia	Ellada Sotiridou	Received

P3-144	A case of paediatric GH-secreting pituitary adenoma apoplexy	Dario Gallo	Received

P2-144	Glucagon therapy in preterm infants with hyperinsulinemic hypoglycaemia	Roschan Salimi Dafsari	Received

P2-145	NEONATAL HYPO-KETOTIC HYPOGLYCEMIA SECONDARY TO TRANSIENT HYPERINSULINISM. DIAZOXIDE RESPONSIVENESS AND EXPERIENCE WITH FASTING TEST AFTER TREATMENT WITHDRAWAL	Luis Salamanca	Received

P1-145	The investigation of genetic etiology in familial cases with congenital hypothyroidism	Feyza Darendeliler	Received

P3-146	GROWTH HORMONE DEFICIENCY AFTER RADIATION THERAPY FOR BRAIN TUMOR HOW TO MANAGE ?	OUIDAD BAZ	Received

P2-146	Severe Neonatal Hyperparathyroidism Due to a Novel Homozygous Mutation of the Calcium-Sensing Receptor (CaSR)	amir hacohen solovitz	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

P1-147	Intrathyroidal ectopia of thymus in children: frequency, ultrasound, evolution.	Goar Okminyan	Received

P2-147	A rare cause of pediatric hypoglycemia in a boy: a malignat insulinoma	Mariella Valenzise	Received

P1-148	Activating mutation M453V in receptor TSHR as a cause familial hyperthyroidism	Beata Sawicka	Received

P1-149	Central hypothyreoidism with pituitary enlargement and no gene alterations	Zoran Gucev	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

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

P3-150	Features of somatropin replacement therapy in a patient with Floating Harbor Syndrome	Olga Berseneva	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

P3-152	Linear Growth of infants with neonatal and early infantile meningitis	Ashraf Soliman	Received

P1-152	THYROID FUNCTION FOLLOWING HEMITHYROIDECTOMY IN A PEDIATRIC COHORT	Patricia Papendieck	Received

P2-152	Congenital Hyperinsulinism due to Compound Heterozygous mutations in ABCC8 fully responsive to Diazoxide therapy.	Tashunka Taylor-Miller	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

P1-153	Homozygous c.2422delT hTPO mutation in three patients with congenital hypothyroidism followed over 20 years	Kalina Mihova	Received

P3-153	Prevalence of Thyroid Dysfunction and Associated Autoimmune Disorders in Young Children with Down Syndrome (DS); A Cohort Study.	Nada Alaaraj	Received

P1-154	Association of Hashimotos Thyroiditis with Antistreptolysin O titer.	Antonis Voutetakis	Received

P2-154	Determinants of the peak GH response of the glucagon stimulation test in slowly growing children.	Jean De Schepper	Received

P3-155	Turners Syndrome - clinical presentation, genetics, investigation and management: a 10-year review	Hassan Elechi	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

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

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

P3-157	Bardet-Biedl syndrome: a case series	Ana Raquel Mendes	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

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

P3-158	A novelvariant of KAT6B caused Say-Barber-Biesecker-Young-Simpson syndrome	Ying Weng	Received

P2-158	Clinical and genetic characteristics of eleven Korean patients with hypochondroplasia and outcomes of growth hormone therapy.	Min-Sun Kim	Received

P1-159	Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency	Zehra Yavas Abali	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

P3-159	THREE CASES WITH FAMILIAL SHORT STATURE: LERI-WEILL SYNDROME	Hayrullah Manyas	Received

P1-160	Serum fetuin-A and insulin levels in classic congenital adrenal hyperplasia	Erdal Kurnaz	Received

P2-160	METABOLIC OUTCOME IN ADOLESCENTS WITH GROWTH HORMONE DEFICIENCY DURING TRANSITION PHASE	Nicola Improda	Received

P3-160	Thyroid Dysfunction in the First Year of Life in Infants with Down syndrome: Linear Growth Over 4 Years.	Nada Alaaraj	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

P1-161	Perioperative control of blood pressure in a child with paraganglioma using Esmolol	AMIR BABIKER	Received

P2-161	The Influence of pituitary MRI findings on clinical presentation and growth in GH-Treated Children with Congenital Hypopituitarism	Adel DJERMANE	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

P2-162	Metabolic effects of growth hormone treatment in short prepubertal children: a double-blinded randomized clinical trial	Anders Tidblad	Received

P3-163	Endocrinological evaluation of male patient with Floating-Harbor syndrome case report	Maja Oko&324;ska	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

P1-164	The urinary steroid signature of premature adrenarche	Marco Janner	Received

P2-164	BRAIN MAGNETIC RESONANCE IMAGING IN CHILDREN WITH ISOLATED GROWTH HORMONE DEFICIENCY	Pamela Yesquen	Received

P3-164	Longitudinal evaluation of audiological pattern in Turner syndrome	Tommaso Aversa	Received

P2-165	The clinical significance of post-sleep growth hormone levels in the diagnosis of growth hormone deficiency	Chaeri Yoo	Received

P1-165	How the level of antibodies against 21-hydroxylase changes with time in patients with Addisons disease	Leila Sozaeva	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

P1-166	Cortisol levels in glucagon stimulation tests in children evaluating for short stature: clinical and laboratorial correlations	Athanasios Christoforidis	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

P3-166	Growth hormone treatment and puberty in patient with Pallister-Hall syndrome.	Elena Pisareva	Received

P3-167	Bloom Syndrome in 7-year-old girl diagnosed with short stature.	Hanna Borysewicz-Sa&324;czyk	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

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

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

P1-168	Genotype-phenotype characteristics in four families of type 2 collagenopathy in our hospital	Kenichi Yamamoto	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

P3-169	Schaaf-Yang syndrome:Three cases report of MAGEL2 variation and literature review	Xuefei Chen	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

P3-170	Reevaluation of congenital growth hormone deficiency in adulthood	imen gargouri	Received

P1-170	Efficacy and safety of denosumab treatment in a prepubertal patient with cherubism	Haruka Kawamura	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

P2-171	Final height in GH-deficient paediatric patients: a nationwide experience	Stefano Zucchini	Received

P3-172	Pure gonadal dysgenesis with partial testicular development associated with Turner syndrome with SRY	Kyung Hee Yi	Received

P2-172	DIFFERENCES OF EFFICIENCY OF TREATMENT OF ISOLATED GROWTH HORMONE DEFICIENCY AND PANHYPOPITUITARISM IN CHILDREN IN REAL CLINICAL PRACTICE	Ekaterina Rudkova	Received

P3-173	A case of WiedemannSteiner syndrome with central precocious puberty	Kohei Aoyama	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

P2-173	Implementation of a growth disorders related twinning program in pediatric endocrinology is it necessary and feasible?	Irina Halvadzhiyan	Received

P1-174	The Optimal Dosage of Vitamin D Supplement for Vitamin D deficiency in Korean Children and Adolescents	Seung Yang	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

P3-174	Population prevalence of Downs syndrome and cardiac complications in South Korea: Based on National Health Insurance Service (NHIS)	NA YEONG LEE	Received

P2-175	The impact of Growth hormone treatment in patients with Noonan syndrome and growth hormone deficiency	Hae Sang Lee	Received

P3-175	McCune Albright Syndrome: Two cases with different clinical courses.	Agim Gjikopulli	Received

P1-175	Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees	Sare Betul Kaygusuz	Received

P1-176	Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA	Sare Betul Kaygusuz	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

P1-177	Severe Hypocalcaemia in Propionic Acidaemia caused by Parathyroid Hormone Resistance and treated with Alfacalcidol.	Jessica Sandy	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

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

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

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

P2-179	UNUSUAL CASE OF PATIENT WITH KLINEFELTER SYNDROME WITH SHOX DELETION BORN TO THE MOTHER WITH LERI-WEILL DYSCHONDROSTEOSIS	Nevena Krnic	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

P3-179	Clinical and molecular characteristics of pediatric patients with multiple endocrine neoplasia (MEN)	Yena Lee	Received

P3-180	APECED Syndrome in Childhood: Rare Clinical Presentations to Keep in Mind	Semra etinkaya	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

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

P3-181	Phenotype and clinical course in three individuals with Multiple Endocrine Neoplasia Type 2A due to a RET gene mutation.	Evangelia Panou	Received

P1-181	A case of prohormone convertase deficiency diagnosed with type 2 diabetes mellitus	Senay Savas-Erdeve	Received

P3-182	Two Siblings Case with Diagnosis of Autoimmune Polyglandular Syndrome Type 1	Hayrullah Manyas	Received

P2-182	Auditory phenotypes and dynamics of hearing thresholds in 246 Turner syndrome females	Tommaso Aversa	Received

P1-182	The influence of excess iron on pancreatic beta cells	Lina ZHANG	Received

P3-183	High demand for collaborative work between paediatric endocrinologists in Arab countries	Hussain Alsaffar	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

P1-183	Study on the mechanism of metformin in improving PGRN-induced insulin resistance of 3T3-L1 cell	Siqi Huang	Received

P1-184	A case with monogenic diabetes caused by RFX6 mutation in a 14-year-old-girl	Jeesuk Yu	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

P3-184	Eosinophilic Ascites: a rare complication of autoimmune polyendocrinopathy	Zacharoula Karabouta	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

P1-185	Endothelial and heart dysfunction in children and adolescents with type 1 diabetes.	Barbara Predieri	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

P2-186	Clinical features in a patient with Turner syndrome and pericentric inversion of chromosome 9	Mariella Valenzise	Received

P3-187	Difficulties in hypothyroidism and diabetes treatment in patient with GATA6 gene mutation case report.	Maja Oko&324;ska	Received

P2-187	Less Ready for Adulthood? Turner syndrome has an impact on transition readiness	Caroline Culen	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

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

P3-188	Endocrinopathies and linear growth in adolescents with -thalassemia intermedia in Relation to liver iron content.	Ashraf Soliman	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

P1-189	A Novel SLC2A2 mutation implicated in Fanconi Bickel syndrome and dysglycemia	Sanaa Sharari	Received

P3-189	Bardet-Biedl syndrome: Not only what but also how matters?	Narjess Boutalbi	Received

P3-190	STRUCTURAL PITUITARY ABNORMALITY AND DYSFUNCTION ASSOCIATED WITH CHARGE SYNDROME	Feneli Karachaliou	Received

P2-190	Growth Hormone Therapy in patients with Noonan Syndrome	Louise Apperley	Received

P1-191	Effect of Probiotics intake on obese children	Ruimin Chen	Received

P3-191	Hormone-secreting pituitary adenomas in children and adolescents	Natallia Akulevich	Received

P3-192	ROHHAD SYNDROME: REPORT OF 2 RARE CASES FROM CRETE-GREECE	PINELOPI SMYRNAKI	Received

P1-192	Changes in objectively measured sleep quality after an integral intervention in patients with abdominal obesity	Cristina Azcona	Received

P2-192	SHOX-HAPLOINSUFFICIENCY INTRA-FAMILIAL PHENOTIPIC VARIABILITY AND THE IMPACT ON FINAL HEIGHT: REPORT OF A PEDIGREE	Maria Cristina Maggio	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

P1-193	Circulating Insulin-like Growth Factor-I independently predicts blood pressure in apparently healthy children	Abel López-Bermejo	Received

P3-194	Coincidental Central Precocious Puberty and Wilms Tumor	ramona nicolescu	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

P2-195	The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation	Ayse Pinar OZTURK	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

P2-196	KLINEFELTER SYNDROME ASSOCIATED WITH SHORT STATURE DUE TO IATROGENIC CUSHING	RENATA PINTO	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

P3-197	Central precocious puberty in a boy with Prader-Willi syndromeduring growth hormone replacement therapy	WEI LU	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

P1-198	Correlation of serum chemerin concentrations with obesity/metabolic syndrome characteristics in pre-adolescents and adolescents	FLORA BACOPOULOU	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

P3-198	A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation	Ayhan Abac&305;	Received

P3-199	Prolactinomas in a Pediatric Population.	liliana Mejia de Beldjenna	Received

P1-199	Non-alcoholic fatty liver youth with obesity	Marina Ybarra	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

P2-200	Endocrine Features of Schaaf-Yang syndrome. Case report.	Olena Tolstikova	Received

P2-201	Papillary thyroid cancer in a 17-years old girl with a late-diagnosed Turner syndrome	Maria Pankratova	Received

P1-201	Serum Kisspeptin in Obese Children and Its Relation to Glucose Metabolism	Kochakorn Sithinamsuwan	Received

P2-202	The applicability of the NH-Clinical scoring system on diagnosis of Iranian children with SRS	Somayyeh Hashemian	Received

P3-202	A Case Of Syndromic Hypopituitarism	Sare Betul Kaygusuz	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

P1-203	Serum nonylphenol and obesity in children and adolescents	Mi Jung Park	Received

P3-203	Anapylaxis Secondary to Gonadotrophin Releasing Hormone Agonist used for Precocious Puberty, Two Case Reports	Hala Shaikh	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

P2-204	Electromagnetic fields exposure in Adolescents: a survey in 11-14 y old Greek students	Styliani Geronikolou	Received

P1-204	Risk factors for brain injury after transient or persistent hyperinsulinemic hypoglycemia in neonates	Marcia Roeper	Received

P1-205	Central Hypoventilation Syndrome and Hyperinsulinaemic Hypoglycaemia	Antonia Dastamani	Received

P3-205	Childhood craniopharyngioma: a single centre experience	Dario Gallo	Received

P2-205	Subcutaneous ossifications in children - think about AHO	Monika Flury	Received

P3-206	Unusual cause of hypopituitarism : A Niemann Pick Disease	Mouna Mnif Feki	Received

P2-206	Growth outcomes in growth hormone treated indian children with celiac disease	Smita Ramachandran	Received

P1-206	Unusual congenital hyperinsulinism case in a patient with a pathogenic GCK mutation	Diliara Gubaeva	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

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

P2-208	Autoimmune polyendocrine syndrome type I: a neuroendocrine multi-systemic disease with a variable expressivity	Gerdi Tuli	Received

P3-209	Pituitary hyperplasia as a complication of severe hypothyroidism due to Hashimotos thyroiditis could impair pituitary function.	Domenico Corica	Received

P1-209	Urogenital abnormalities in children conceived by assisted reproductive technologies	Zinaida Zyuzikova	Received

P2-209	Endocrine complications of patients with hepatic type of glycogen storage disease	Yena Lee	Received

P1-210	Subcutaneous fat necrosis of the newborn: A systematic review of the literature	Stephanie Brandt	Received

P3-210	Homozygosity for Proopiomelanocortin (POMC) mutation in a Palestininan child	Abdulsalam Abu-Libdeh	Received

P2-210	Autoimmune Thyroiditis and Autoimmune Hepatitis presenting at onset of Type 1 Diabetes (T1D)	Alice Marchant	Received

P3-211	Peculiarities Of Clinical Options For Delaying Sexual Aging In Boys-Adolescents	Hanna Kosovtsova	Received

P1-211	Characteristics of children with Kabuki syndrome and hyperinsulinemic hypoglycemia	Henrike Hoermann	Received

P2-211	Ulnar mammary syndrome - a case report	Supreetha Shetty	Received

P2-212	Unusual ovary formation in a girl with McCune-Albright syndrome.	Nadezhda Makazan	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

P1-213	Determinants of final height in patients born small for gestational age treated with recombinant growth hormone.	elodie adler	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

P2-213	Heart rate variability in adolescent polycystic ovary syndrome Greek patients	Styliani Geronikolou	Received

P2-214	CELIAC DISEASE AND ENDOCRINE AUTOIMMUNITY IN CHILDREN AND ADOLESCENTS	Feneli Karachaliou	Received

P3-214	Central precocious puberty in a 2 year-old with no sinister cause.	Sharon Lim	Received

P3-215	MKRN3 Gene Mutation in a Case of Familial Central Precocious Puberty	Berna Ero&287;lu Filibeli	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

P2-215	Intestinal ganglioneuromatosis as first manifestation of multiple endocrine neoplasia 2B in a premature girl	Tina Leunbach	Received

P3-216	Family Central Early Puberty about Three Sisters	Mouna Mnif Feki	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

P3-217	Clinical and Molecular Spectrum of Patients with Disorders of Sex Development: A Single Center Experience	Samim zen	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

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

P2-219	Aromatase inhibitor treatment in patient with beta-human chorionic gonadotrophin secreting tumor and gonadotropin-independent precocious puberty.	Nadia Mazerkina	Received

P3-219	Final adult height in SRY-negative 46,XX ovotesticular differences of sex development individuals.	Maria Tereza Ferrari	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

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

P3-220	A rare cause of SRY (-) 46, XX DSD: Aromatase deficiency	TULAY TULAY	Received

P3-221	Gonadal dysgenesis, 46 XY about 5 familial cases	Mouna Mnif Feki	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

P2-221	The case of congenital hypopituitarism due to mutation POU1F1 in 3 azerbaijani newborn boys.	Anzhelika Arestova	Received

P2-222	Case report of syndrome of nephrogenic inappropriate antidiuretic hormone secretion (NSIADH) caused by rare AVPR2 gene active mutation	wenjing li	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

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

P2-223	Long term effects of GnRH agonist therapy on BMI in girls with idiopathic central precocious puberty	Dogus Vuralli	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

P2-224	To whom should central nervous system imaging be performed in girls with central precocious puberty (CPP)?	Dogus Vuralli	Received

P3-224	Clinical and laboratory characteristics of different various types of gonadal dysgenesis in girls with hypergonadotropic hypogonadism	Kseniya Kabolova	Received

P2-225	Unusual presentation of McCune-Albright syndrome in a 10-year-old girl	sara ciccone	Received

P1-225	The Phenotypic Spectrum of Kabuki Syndrome in Patients of Chinese Descent	YiRou Wang	Received

P3-225	Evaluation of the Role of Fetuin A in Pathophysiology of Polycystic Ovarian Syndrome in Adolescents	Elvan Bayramoglu	Received

P3-226	Rare Cause of 46,XY Sexual Development Disorder: 17-Hydroxysteroid Dehydrogenase Type 3 Deficiency	Hayrullah Manyas	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

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

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

P2-227	Screening of Central Precocious Puberty (CPP) in females: efficacy of morning unstimulated luteinizing hormone (mLH) levels	Federico Baronio	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

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

P1-229	Endocrine evaluation of 29 Cornelia de Lange Syndrome patients (CdLS) patients	ANGELA MARINA ASCASO MATAMALA	Received

P3-229	Primary amenorrhea revealing Leydig cell hypoplasia	imen gargouri	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

P3-230	Novel heterozygous mutation in Wilms tumor 1 gene in patient with mixed gonadal dysgenesis	Heba Hassan	Received

P2-230	The incidence and diagnostic factors of polydipsia and polyuria: a single center survey in Japan	Miyuki Kitamura	Received

P2-231	Macroprolactinoma presenting with Pituitary Apoplexy associated with middle cerebral artery infarction in an adolescent male.	Sally Newbold	Received

P1-231	Height and weight dynamics in preschool boys with constitutional delay of growth and puberty	Thomas Reinehr	Received

P3-231	Falsely elevated serum sex steroid hormones in a girl with premature adrenarche	Lavinia La Grasta Sabolic	Received

P2-232	Childhood craniopharyngioma: clinical picture at diagnosis in an Italian multicentre study	Daniela Driul	Received

P1-232	Two Chinese Children with FBN1-Related Acromelic Dysplasia	Lele Hou	Received

P3-232	NR5A1 Gene Mutation: Variable Phenotypes, New Variants, Different Outcomes	Maria Felicia Faienza	Received

P3-233	Early embryonic testicular regression syndrome presenting with female external genitalia	Sezer Acar	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

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

P3-234	Diagnostic Dilemma in a 46-XY Female	Richelle Waldner	Received

P2-234	Evaluation of Clinical Features and Treatment Responses of Cases with Hyperprolactinemia	servan ozalkak	Received

P1-235	Development of a measure for the impacts of pediatricachondroplasia on childrens daily functioning and well-being	Jane Beck	Received

P2-235	A Case of Gonadotropin-independent precocious puberty due to germ cell tumor in the frontal lobe	Bulent Hacihamdioglu	Received

P3-235	Leydig Cell Hypoplasia in Three Siblings in the Same Family	Hakan Doneray	Received

P3-236	KLINEFELTER SYNDROME PRESENTING WITH LEARNING DISABILITIES: CASE REPORTS	Paraskevi Zosi	Received

P1-236	Serum endocan levels as a marker of endothelial dysfunction in Turner syndrome and correlation with cardiac findings	Ali Genco Genay	Received

P3-237	Gender self-identification and intra-family relations in children with disorders of sex development	Eugenia Globa	Received

P2-237	Heterozygous OTX2 deletion in a boy with normal eye development and normal pituitary function.	Emese Boros	Received

P1-237	The Effects of Fetal Electromagnetic Field Exposure on Expression of Anxiety Behavior and Associated Genes in Adolescent Period	Bertan Yilmaz	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

P3-238	Bilateral testicular atrophy and normal Inhibin B level : A paradoxal clinical finding for a rare biochemical cause	wafa kallali	Received

P2-238	Risk Factors for Hypogonadism in Patients with -Thalassemia Major:A Cross-sectional study	Zhuan-nan Jiang	Received

P1-239	UNUSUAL PRESENTATION OF AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE 1 (APS1)	Yagmur Unsal	Received

P2-239	Radiation therapy for children with medulloblastoma: Growth and thyroid sequelae.	Beatriz Corredor-Andrés	Received

P3-239	NORMOSMIC HYPOGONADOTROPIC HYPOGONADISM: AN INTRAFAMILIAR CASE	Joana Soares	Received

P1-240	Association of Tuberous sclerosis complex (TSC) and Insulinoma in a pediatric patient	ANA TANGARI	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

P1-241	A novel DCAF17 homozygous mutation in a girl with Woodhouse-Sakati syndrome and its role in the endocrine glands	Erdal Kurnaz	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

P3-242	CLINICAL AND LABORATORY CHARACTERISTICS OF PATIENTS WITH DIFFERENT VARIANTS OF GONADAL DYSGENESIS	Ekaterina Sannikova	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

P1-242	Basal metabolic rate in polycystic ovary syndrome: a meta-analysis	Styliani Geronikolou	Received

P3-243	Etiologic Classification of 46, XY Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results	Ayla Guven	Received

P2-243	A case of severe recurrent hypoglycemia after traumatic brain injury	Dr. Bongsebandhu-phubhakdi	Received

P1-243	A nation-wide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in pediatric and adolescent cancer patients	Yoko Miyoshi	Received

P2-244	The Evolving Role of Whole Exome Sequencing in the Diagnosis of Disorders of Sex Development (DSD)	Yardena Tenenbaum-Rakover	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

P1-244	Two Different Endocrine Cancer, One Disease; DICER-1 Mutation	Nihal Hatipo&287;lu	Received

P2-245	ETIOLOGICAL STRUCTURE DISORDERS OF SEX DEVELOPMENT 46,XY BY ONE CENTER	Ekaterina Sannikova	Received

P1-245	PTEN Hamartoma Tumor Syndrome (Overlap of Cowden syndrome and the Bannayan-Riley-Ruvalcaba Syndrome): Case Report	Hayrullah Manyas	Received

P3-245	Ovarian insufficiency: the hidden uterus	Biwen Cheng	Received

P3-246	An Adolescent Girl Presented with Hoarseness of Voice	Ho-chung YAU	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

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

P1-247	One AIRE gene mutation and two different clinical manifestations in a couple of brothers	Tiziana Timpanaro	Received

P2-247	DOES THE ANOGENITAL DISTANCE PREDICT OUTCOME OF HYPOSPADIAS REPAIR?	Alexander Springer	Received

P3-247	Turners syndrome mosaicism 45X/47XXX with iron deficiency anemia due to menometrorrhagia	Hwal Rim Jeong	Received

P3-248	Difficulties in diagnosing variable disorders of sexual development	Elena Sukarova-Angelovska	Received

P1-248	A novel AIRE gene mutation in two siblings revealing different phenotypes of autoimmune polyendocrine syndrome type 1	Melek Yildiz	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

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

P3-249	Association of Subclinical Hypothyroidism and Dyslipidemia in Children and Adolescents	Ashkan Habib	Received

P1-250	Correlation between pubertal growth and testicular volume in boys a longitudinal study	Anton Holmgren	Received

P3-250	Evaluation of Clinical, Demographic Data and Treatment Results of Cases with Graves Disease	Ayhan Abac&305;	Received

P2-250	High prevalence GnRH receptor mutations in Russian patients with idiopathic hypogonadotropic hypogonadism	Elena Frolova	Received

P3-251	A case of Graves disease with negative thyrotropin stimulating antibodies in a pediatric patient with type 1 diabetes	Liliana Burdea	Received

P1-251	Central diabetes insipidus in children: role of GH antibodies	Flavia Napoli	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

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

P1-252	Brain Malformations and Sellar Spine as possible causes of Central Precocious Puberty in a large monocentric study	Daniela Fava	Received

P3-252	An unusual presentation of Hypothyridism: Van Wyk-Grumbach syndrome	imen gargouri	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

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

P3-253	Child thyrotoxicosis Syndrome: Structure and Characteristics.	Oleg Latyshev	Received

P1-254	A novel approach for the evaluation of hypothalamic-pituitary region in patients with growth hormone deficiency: Pons ratio	Edip Unal	Received

P2-254	Paediatric Health Assistance to Transsexual Minor in the Multidisciplinary Care Unit of the Basque Country (Spain)	Itxaso Rica	Received

P3-254	Encephalitis associated with autoimmune thyroiditis : a rare cause of encephalopathy in children.	Julie Fudvoye	Received

P1-255	Effects of 5-Hydroxymethylfurfural on Pubertal Development of Wistar Rats	Selin Elmaogullari	Received

P3-255	Association of BMI Z-score and Subclinical Hypothyroidism in Children and Adolescents	Ashkan Habib	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

P1-256	Kisspeptin levels is a new diagnostic approach of hypogonadotropic hypogonadism in boys.	Irina Nikitina	Received

P3-256	Pseudoprecocious Puberty in a Girl with Untreated Acquired Hypothyroidism	Mihaela Dimitrova-Mladenova	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

P2-257	Efficacy and short-term safety of testosterone treatment in adolescents with gender dysphoria	Sabine Hannema	Received

P3-257	Bilateral Hip Pain as First Symptomatic Expression of Severe Primary Hypothyroidism	ramona nicolescu	Received

P3-258	The challenge to treat neonatal autoimmune hyperthyroidism in a small preterm	Sarah Lignitz	Received

P2-258	Study of Autistic Features among children and adolescents with Congenital Adrenal Hyperplasia	Shaymaa Elsayed	Received

P1-258	Novel pubertal references for girls using ultrasound to stage breast development. The Bergen Growth Study 2.	Ingvild Bruserud	Received

P3-259	Graves disease in a 3 year-old patient with agranulocytosis due to methimazole	emine demet akba&351;	Received

P1-259	Disruption of Hypothalamic regulation of Appetite associated with Proton Beam Therapy	aashish sethi	Received

P2-259	Differences of sex development with chromosomal mosaicism: histological characterization and immunohistochemistry markers in gonads during childhood.	Natalia Perez Garrido	Received

P3-260	Hashimotos Thyroiditis in children: Case series report of three patients	Thanh Nguyen Trong	Received

P2-260	Heterozygous CYP11A1 mutation associated with 46XY Disorder of Sexual Differentiation and mild Adrenal Insufficiency	Philippa Bowen	Received

P1-260	A case-control study of exposure to bisphenol-A and phthalates in girls with early onset of puberty	annalisa deodati	Received

P1-261	Long-term urological and psychosexual outcome of men born with hypospadias	Lloyd Tack	Received

P2-261	The modern approaches to differential diagnosis of constitutional delay of puberty and hypogonadotropic hypogonadism in boys	Oleg Latyshev	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

P3-262	A 12 year old boy with multifocal papillary thyroid carcinoma	Nataliia Muz	Received

P2-262	Etiologic Classification of 46, XX Disorders of Sexual Differentiation According to Chicago Consensus: Single Center Results	Ayla Guven	Received

P1-262	Long-Term Outcome In Leydig Cell Hypoplasia	Alessandra Boncompagni	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

P3-263	Papillary Thyroid Cancer in Children: Single Center Results	gl direk	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

P2-264	Ethical and familial dilemmas of genitoplasty encountered in Congenital Adrenal Hyperplasia	Dirlewanger Mirjam	Received

P1-265	Dynamics in blood pressure after pubertal suppression with GnRH analogs followed by testosterone treatment in male adolescents	Liat Perl	Received

P2-265	Hormonal assessment of malformation syndromes associated with disorders of sex development: Case series of 9 patients	Shaymaa Mahfouz	Received

P3-266	A Novel Mutation of INSR Gene in a Child with Type A Insulin Resistance	Federica Verdecchia	Received

P1-266	A Nationwide Study Of The Prevalence & Initial Management Of Atypical Genitalia & Delayed Sex Assignment In The Newborn	Salma Ali	Received

P2-266	Family Perrault syndrome in two Tunisian sisters	Mouna Mnif Feki	Received

P2-267	An intriguing co-occurrence of MURCS and VACTER associations	Noa Shefer Averbuch	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

P1-267	Endocrine profiling and association with testicular volume and biometrics in a cohort of Norwegian boys	Andre Madsen	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

P1-268	Idiopathic scoliosis in girls with central precocious puberty: Incidence and effect of gonadotropin-releasing hormone agonists	Lindsey Yoojin Chung	Received

P2-269	Pseudo-precocious puberty in children triggered by incidental transdermal contamination with topical sex steroids through parents	Vira Yakovenko	Received

P3-269	IGSF1 mutation: treatment in the absence of symptoms?	Sarah Castets	Received

P1-269	The impact of Klinefelter Syndrome on quality of life a multicentre study	Sebastian Franik	Received

P1-270	Large spectrum of DSD phenotype caused by pathogenic variants in Wilms tumor suppressor gene 1.	Maria Tereza Ferrari	Received

P3-270	Real World Experience of Burosumab Therapy in Children with X-linked Hypophosphataemic Rickets - 12 month follow-up data	Jessica Sandy	Received

P2-270	FOLLOW-UP OF INDIVIDUALS WITH GENDER IDENTITY DISORDERS: A LONG AND CHALLENGING PROCESS	Esin Karakilic Ozturan	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

P2-271	Follow-up of two similar patients with Steroidogenic Factor-1 (SF-1/ NR5A1) variants, in two different eras	Odile Gaisl	Received

P1-271	Endocrine and reproductive outcome of men born with various degrees of hypospadias	Lloyd Tack	Received

P1-272	Age at menarche over the last decades and inter-regional variability in Northern Spain	Pablo Alonso Rubio	Received

P2-272	Genetic testing of DSD patients in Ukraine	Eugenia Globa	Received

P1-273	Hypergonadotropic hypogonadism in 46, XX adolescents without gonadotoxic therapy: Clinical features and molecular etiologies	Zehra Yavas Abali	Received

P2-273	Spectrum of genital abnormalities in Robinow syndrome: Case series.	Shaymaa Mahfouz	Received

P3-273	THE INCREASE IN ADIPOSE TISSUE DURING GH TREATMENT INDUCES INSULIN RESISTANCE	Zvi Laron	Received

P2-274	MAMLD 1 gene mutation and 46 XY sex development disorder : a case report	BOUCHRA BOUSYF	Received

P1-274	Quality of life in Chilean transgender children, adolescents, and their parents	Carolina Mendoza	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

P3-275	Serum spexin is correlated with lipoprotein(a) and androgens in normal-weight, overweight and obese adolescent females	FLORA BACOPOULOU	Received

P2-275	46,XYcomplete gonadal dysgenesis in a familial case with a rare mutation in theDesert Hedgehog (DHH) gene	Vassos Neocleous	Received

P1-275	Long-term outcome of testicular function in nonclassic lipoid congenital adrenal hyperplasia	Tomohiro Ishii	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

P2-276	Novel thyroid hormone receptor -gene mutations in resistance to thyroid hormone	Ga Hyun Lee	Received

P2-277	Congenital Hypothyroidism: neonatal screening program with T4 and TSH.	Maria Chueca	Received

P3-277	The Role of Urine AVP in the Diagnostic Pathway of Polyuria and Polydipsia Syndrome	Claudio Giacomozzi	Received

P2-278	A 10- year-old girl with thyroid hormone resistance (THR)- case report.	Artur Bossowski	Received

P3-278	NEW MUTATION OF GNAS IN A 2 YEAR OLD ONCOLOGICAL PATIENT	Ana Belen Ariza Jimenez	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

P2-279	DIAGNOSIS OF CENTRAL CONGENITAL HYPOTHYROIDISM AND MULTIPLE PITUITARY DEFICIENCIES THROUGH A NEONATAL SCREENING PROGRAM.	Gema Grau	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

P2-280	CHILDHOOD THYROID CANCER AFTER RADI OIODINE THERAPY	OUIDAD BAZ	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

P2-281	Differential diagnosis of euthyroid hyperthyroxinemia	Eugenia Globa	Received

P3-281	New Autosomal Dominant Mutation in Glucokinase Gene Causing Congenital Hyperinsulinism Diagnosed in Adulthood	Ilana Zalmon-Koren	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

P1-282	Characteristics of 311 children with early onset pubertal signs. Descriptive study	paula sol ventura wichner	Received

P2-282	Treatment for Graves Disease in Children and adolescents: A Long-Term Retrospective Study at a Single Institution	Min-Sun Kim	Received

P2-283	Changes of thyroid function in girls with central precocious puberty after 6-month GnRH agonist treatment	Young-Jun Rhie	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

P1-283	Children with Hashimotos thyroiditis have increased intestinal permeability: Results of a pilot study	Banu Kucukemre Aydin	Received

P1-284	Different Endocrine Affects in DICER-1 Syndrome	semra etinkaya	Received

P2-284	Papillary Thyroid Cancer Associated With Hyperthyroidism	AHU PAKET&304;	Received

P3-284	Demographic, clinical and biochemical characteristics of pediatric obesity: interim analysis of a larger prospective study	Maja Tankoska	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

P1-285	Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases	AHU PAKET&304;	Received

P2-285	Serum PTH does not correlate with their serum calcium levels in children and adolescents with Hashimoto thyroiditis	Hirohito Shima	Received

P2-286	Management of childhood thyroid nodules in children a large group of cases from a single center.	Joanna Sieniawska	Received

P3-286	Alterations in ambulatory blood pressure in adolescents with obesity.	Desiree LOPEZ-GONZALEZ	Received

P1-286	Identification of a THRA mutation in a 2yr old child with clinical features of hypothyroidism and multisystem involvement	Rajesh Sakremath	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

P3-287	Should we review clinical criteria to diagnose SHOX gene mutations?	Francesco Gallo	Received

P2-287	BONE HOMEOSTASIS IN CHILDREN WITH SUBCLINICAL HYPOTHYROIDISM: EFFECTS OF TWO-YEARS TREATMENT WITH LEVOTHYOXINE	Flavia Barbieri	Received

P1-288	Outcomes of persistent hyperthyrotropinaemia in well term infants	May Ng	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

P1-289	Thyroid peroxidase antibodies in children with HLA-conferred susceptibility to type 1 diabetes	Liisa Saare	Received

P3-289	Quality of Life of patients with Type 1 Diabetes.	Renata Markosyan	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

P2-290	A rare combination with Congenital Hypothyroidism - Brain Lung Thyroid Syndrome	Sajith Sandamal	Received

P3-290	Etiologies and clinical patterns of Hypopituitarism in Sudanese children	Samar Hassan	Received

P1-291	An incidental finding of thyroid hormone resistance due to a de novo mutation in the THRB gene	Noa Shefer Averbuch	Received

P3-291	Rare causes for paediatric virilizing tumors	Jananie Suntharesan	Received

P1-292	Outcome of congenital hypothyroidism in Algeria: the urgent need to implement a national newborn screening program	Adel DJERMANE	Received

P2-292	Thyroid autoimmunity in children and adolescents with Type 1 Diabetes Mellitus	Nalini M Selveindran	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

P2-293	Analysis of diabetes-associated autoantibodies in children and adolescents with autoimmune thyroid diseases	Artur Bossowski	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

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

P2-296	Progressive thyroid dysfunction in infants with Down Syndrome; Trisomy 21 (DS): Effect on Linear Growth	Nada Alaaraj	Received

P3-296	Neonatal severe hyperparathyroidism - using genetics to determine treatment	Carmit Avnon-Ziv	Received

P2-297	EVALUATION OF ELEVATED SERUM THYROID-STIMULATING HORMONE (TSH) IN CHILDREN AND ADOLESCENTS: A SINGLE-CENTER STUDY IN URUGUAY.	Mariana Risso	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

P3-297	LIVER TRANSPLANTATION IN SAUDI HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA PATIENTS	Salman Al-Mansour	Received

P3-298	Mitchell-Riley Syndrome, a report of novel mutation in a Palestinian family resulting in Neonatal diabetes	Abdulsalam Abu-Libdeh	Received

P1-298	First morning pregnanetriol and 17-hydroxyprogesterone correlated significantly each other with in 21-hydroxylase deficiency	Tomoyo Itonaga	Received

P2-298	Neonatal hyperthyroidism: our centres experience	Silvana Caiulo	Received

P3-299	Review of neonatal cortisol evaluation between 2012-2018 in a single centre: trends, outcomes and associations.	Taffy Makaya	Received

P2-299	Epidemiological aspects of pediatric thyroid disorders in Western Ukraine	Viktoriya Furdela	Received

P1-299	Medical identification jewellery use in children and young adults with adrenal insufficiency	Georgina Chrisp	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

P1-300	Growth trajectory and final height in children with non classical congenital adrenal hyperplasia	Letteria Anna Morabito	Received

P2-300	The encephalopathy as complication of Hashimoto thyroiditis in children: a wide variety of clinical manifestations	Paola Chiarello	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

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

P1-301	Height in Infants aged 1 year with classic Congenital Adrenal Hyperplasia is related to their urinary Steroid Metabolome	Clemens Kamrath	Received

P3-302	Cognitive and Learning Performance of Children and Adolescents Cancer Survivors	FLORA BACOPOULOU	Received

P1-302	MIRAGE: A Novel Syndromic Form of Primary Adrenal Insufficiency (PAI)	Xinyi Chin	Received

P3-303	Hirsutism in children: pitfalls and diagnostic challenges	Teofana-Otilia Bizerea-Moga	Received

P3-304	Congenital craniopharyngioma - A rare case of congenital hypopituitarism.	Jananie Suntharesan	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

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

P3-306	IMPROVEMENT OF METABOLIC CONTROL IN CHILDREN WITH TYPE1 DIABETES USING CONTINUOUS GLUCOSE MONITORING DEVICES	Estela Gil-Poch	Received

P1-306	Genotype-Phenotype Correlation and Clinical Findings in 145 Patients with Congenital Adrenal Hyperplasia: Single Centre Experience	gizem cilsaat	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

P3-307	Autoimmune thyroiditis in beta thalassemia major after the hematopoietic stem cell transplantation - case report	Maja Tankoska	Received

P3-308	Graves disease: what place in the childs hyperthyroidism?	mohamed samir merad	Received

P1-308	ABCC8 MODY in an Obese Adolescent Misdiagnosed with Type 2 Diabetes	Berna Ero&287;lu Filibeli	Received

P1-309	Level of glycemic control in pediatric patients with type 1 diabetes in Bern: a cross-sectional study	Tanja Zingg	Received

P3-309	Vitamin D status among children and adolescents in an Egyptian cohort: can we predict vitamin D deficiency?	Mona Karem	Received

P1-310	Preliminary results of public health prevention program for diabetic ketoacidosis in children and adolescent	Marko Simunovic	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

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

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

P1-313	Familial versus non-familial type-2 diabetes mellitus in children and adolescents: Clinical and Biochemical Data.	fawziya Alyafei	Received

P3-314	Case report: Hyperglicemic iperosmolar state in a obese prepubertal girl with newly diagnosis of type 2 diabetes	Nella Polidori	Received

P3-315	Associations between pituitary abnormalities and treatment response in children with growth hormone deficiency. First multicenter study in Portugal	Catarina Diamantino	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

P3-316	Epidemiological and socioeconomic CHANGES in the child population from debut DM1 in this 21st century	Ignacio Diez	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

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

P3-318	Novel mutation in HNF4-alpha gene and reclassification of diabetes in a family	Maria Miguel Gomes	Received

P3-319	Systemic lupus erythematosus, Celiac and Hypothyroidism complicating type 1 diabetes: a rare tetrad.	Rakhi Jain	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

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

P3-320	EpiPEG-PreMeb study: chemerina plasmatic and metabolic syndrome relation at SGA childrens	Ignacio Diez	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

P3-321	Hydrometrocolpos due to congenital adrenal hyperplasia A rare cause of bladder outflow tract obstruction in a female child	Jananie Suntharesan	Received

P3-322	Bartter syndrome complicated with growth hormone deficiency due to a suprasellar arachnoid cyst.	Fathima Raihana Hashim	Received

P1-322	Neonatal diabetes and Glis3 mutation: a new phenotype	Sana Kmiha	Received

P1-323	Diabetes type 2 in non-obese neurologically impaired children and adolescents: a new emerging entity?	Valeria Calcaterra	Received

P3-324	Hypoglycemia in a patient with Turner syndrome and Kabuki make-up	ziqin liu	Received

P1-324	Cataract in type 1 diabetes mellitus patients- a nationwide population-based study	Li-Min Chen	Received

P3-325	45X/47XXX Mosaicism and progressive puberty	ziqin liu	Received

P1-325	Association of CTLA-4 gene with the familial diabetes mellitus	Talat Saatov	Received

P3-326	VITAMIN D AND TYPE 1 DIABETES MELLITUS IN CHILDREN	Harjoedi Adji Tjahjono	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

P1-327	The Paediatric Diabetes Service in England and Wales Learning from Swedens Improvement Journey.	Megan Peng	Received

P3-327	Severe hypercalcaemia after years on the ketogenic diet: A novel case report	Jessica Sandy	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

P3-328	Estrogen Production by Sertoli cell tumor in unusual case of Testicular feminization syndrome	shahab noorian	Received

P3-329	Dysphagia and dyspnea by lingual thyroid mass in a young child: what to do?	mohamed samir merad	Received

P1-329	Evaluation of AGP reports in patients with type 1 diabetes using intermittently viewed continuous glucose measurement system (iCGM)	Erdal Eren	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

P3-330	Van-Wyk Grumbach syndrome associated with trisomy 21: a case report	Nihad Selim	Received

P3-331	Fahr syndrome in young boy with hypoparathyroidism.	mohamed samir merad	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

P3-332	Thyroid cancer in a child with gravess disease	mohamed samir merad	Received

P1-332	Targeted next-generation sequencing demonstrates high frequency of MODY in Russian children.	Natalia Zubkova	Received

P3-333	Influence of nocturnal hypoglycemia on school performance of teens with DM type1	Ignacio Diez	Received

P1-335	The relationship between serum neurotensin levels and metabolic parameters and eating behavior in obese children	Gnl atl&305;	Received

P1-337	How does Clusters of Parental Characteristics Influences Offspring Adiposity: A Prospective Study	Marina Ybarra	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

P1-339	Elevated high-sensitivity C-reactive protein level is associated with prediabetes and adiposity in Korean children and adolescents.	Sohyun Shin	Received

P1-341	ANGPTL2 and ANGPTL3 in children with obesity and metabolic syndrome	Maryam Razzaghy Azar	Received

P1-342	Can Increased First Hour Glucose Concentration in OGTT Be a New Indicator in Projecting Metabolic Profile?	Servan zalkak	Received

P1-343	Perinatal features of Prader-Willi syndrome: a Chinese cohort	Lili Yang	Received

P1-346	Non-invasive assessment of liver steatosis: usefulness of elastography in obese children a pilot study.	Domenico Corica	Received

P1-347	PRECOCIOUS PUBARCHE IN SPINAL MUSCULAR ATROPHY PATIENTS WITH SEVERE SARCOPENIA	Avivit Brener	Received

P1-348	EVALUATION OF THE RELATIONSHIP BETWEEN SERUM URIC ACID LEVEL AND CARDIOMETABOLIC RISK IN OBESE CHILDREN AND ADOLESCENTS	Servan zalkak	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

P1-350	Metabolic risk in long-term survivors of childhood acute lymphoblastic leukemia	Milena Belcheva	Received

P1-351	Congenital generalized lipodystrophy type 4 - New mutation in the CAVIN1 gene	Esra Dger	Received

P1-352	Paediatric patients with type 1 diabetes mellitus exhibit reduced brown adipose tissue heat signature following cold stimulation	James Law	Received

P1-354	Association between adiposity measures and metabolic variables in children and adolescentswith obesity	Giuseppina Rosaria Umano	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

P1-356	The double diabetes in adolescent with Prader-Willi syndrome.	Elena Bogova	Received

P1-357	Evaluation of body composition and resting metabolic rate in adolescents with KS	Daria Bespaliuk	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

P1-359	Insulin-like growth factor 2 in pediatric gliomas: expression, intracellular localization and association with clinical outcome	FLORENCIA CLÉMENT	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

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

P1-363	Metabolism of somapacitan, a long-acting growth hormone derivative, in human subjects	Birgitte Damholt	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

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

P1-366	Glomerular filtration rate in young adults born SGA: a 5-year longitudinal study after cessation of GH treatment.	Wesley Goedegebuure	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

P1-369	Detection and referral of children with short stature in Serbia - the impact of electronic growth charts	Sanja Panic Zaric	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

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

P1-373	Matrix metalloproteinases, their inhibitors and neurotrophic factors as indicators of cardiometabolic risk in Turner syndrome girls	Ewa B&322;aszczyk	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

P1-375	SOAR Study: New approaches to managing social skills deficits in Turner Syndrome	Jeanne Wolstencroft	Received

P1-376	Noonan Syndrome (NS) spectrum panels should include mutations in LZTR1 gene	Maria Guemes	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

P1-378	Vascular Anomalies And Aortic Dilatation in Turner Syndrome Study In A Large Cohort Of Young-Adult Patients	Laura Mazzanti	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

P1-380	A new model of adult height prediction validated in boys with constitutional delay of growth and puberty	Thomas Reinehr	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

P1-382	NUTRITIONAL REQUIREMENTS IN PRADER WILLI SYNDROME CHILDREN TREATED WITH GROWTH HORMONE UNDER TWO YEARS OF AGE	Raquel Corripio	Received

P1-383	Cardiovascular Anomalies and Association with Karyotypes in Turner syndrome in Taiwan: one medical center experience	FU-SUNG LO	Received

P1-384	Pubertal induction amongst girls with Turner Syndrome: a review of changing practice over 10 years.	Hassan Elechi	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

P1-388	Is there a QTc interval prolongation in girls and women with Turner syndrome?	Iris Noordman	Received

P1-389	Eight years of growth hormone treatment in a patient with Schaaf-Yang Syndrome	Alicia Juriaans	Received

P1-390	Genetic Evaluation of Idiopathic Short Stature	Firdevs Bas	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

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

P1-393	Evaluation of body composition and resting metabolic rate in children with growth hormone deficiency	Maria Pankratova	Received

P1-395	Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years	Johanna Hietamki	Received

P1-397	Questioning the Value of Brain MRIs in the Evaluation of Children with Isolated Growth Hormone Deficiency	Ori Eyal	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

P1-399	Pubertal events, reproductive and growth hormones and predictive factors in healthy girls with Transient Thelarche.	JULIO SOTO	Received

P1-400	PLASMA COPEPTIN DISTRIBUTION IN THE PEDIATRIC AGE: A USEFUL DIAGNOSTIC TOOL FOR AVP-RELATED DISORDERS	Gerdi Tuli	Received

P1-401	Management and treatment outcome of childhood-onset craniopharyngioma (CP) in Italy: multicentre collection of 117 cases	Stefano Zucchini	Received

P1-402	EVALUATION OF BRAIN MRI LESIONS IN 381 GIRLS WITH CENTRAL PRECOCIOUS PUBERTY	didem helvac&305;o&287;lu	Received

P1-403	Xanthomatous hypophysitis : a rare case in a paediatric patient	Sze Lyn Jeanne Wong	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

P1-406	Tolvaptan for management of intractable salt and water imbalance in a case with suprasellar tumor after surgery	Tomoe Yamaguchi	Received

P1-407	No association between serum level of NPTX 1 and MKRN3 in central precocious puberty	Hwal Rim Jeong	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

P1-409	LONG-TERM OUTCOME IN YOUNG WOMEN TREATED FOR CENTRAL PRECOCIOUS PUBERTY	Ida DAcunzo	Received

P1-410	Sertoli cell function after chemotherapy in boys with hematologic malignancies	Romina Grinspon	Received

P1-412	WES analysis of a cohort of 94 patients presenting with 46,XY and 46,XX DSD	Patrick Sproll	Received

P1-413	Assessment of the Function of Lower Urinary Tract Following Feminizing Genitoplasty in Females with Congenital Adrenal Hyperplasia	Shaymaa Elsayed	Received

P1-414	Gonadal Insufficiency and Affecting Factors in Patients with Bone MarrowTransplantation(BMT) for Non-malignantIndications in Childhood or Adolescence	Samim zen	Received

P1-415	Clinical and Molecular Characteristics of Russian Patients with 46,XY DSD due to NR5A1 Gene Mutations.	Natalia Kalinchenko	Received

P1-416	Creating a clinicalevaluation system for simple and comprehensive scoring of differences/disorders of sexual development	Fusa Nagamatsu	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

P1-419	Premature ovarian insufficiency in women after treatment for childhoodcancer is a risk factor for metabolic syndrome	Axel Netterlid	Received

P1-420	The Genetic and Clinical Characteristic of Pediatric Patients with Congenital Hypothyroidism Gland In-Situ	Maria Cristina Vigone	Received

P1-421	Zinc transporter 8 (ZnT8) as a new autoantigen in thyroid tissue preliminary data	Artur Bossowski	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

P1-423	Congenital hypothyroidism (CH) detected by the second newborn screening in Lombardia region: incidence and evolution of CH	Silvana Caiulo	Received

P1-424	Transition for patients with chronic thyroid diseases	Piriya Ratnasabapathy	Received

P1-425	Maternally inherited resistance to thyroid hormones with discordant postnatal phenotypes in two infant brothers	Rosalie Cavin	Received

P1-426	A rare case of familial heterozygous Thyroid hormone receptor beta (THRB) mutation presenting with dilated cardiomyopathy	Lucy Hastings	Received

P1-427	Acquired Hypothyroidism in a Toddler: An Unusual Presentation of Langerhans Cell Histiocytosis	Richelle Waldner	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

P1-429	Genetic evaluation of congenital hypothyroidism with gland-in-situ using targeted exome sequencing	Jung hyun shin	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

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

P1-432	LEVOTHYROXINE EFFECT ON THYROID VOLUME IN CHILDREN WITH AUTOIMMUNE HASHIMOTO THYROIDITIS (AHT) PRESENTING SUBCLINICAL (SH) OR OVERT (OH) HYPOTHYROIDISM	Sofia Leka	Received

58th Annual ESPE Meeting

19-21 September 2019 Viena

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ACTIVE FROM 19/09/2019 TO 19/09/2021

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DOI: 10.3252/pso.eu.58ESPE.2019



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