PosterSessionOnline

EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

The 62nd Annual ESPE Meeting 2024

November 16 – November 18 Liverpool

N. Poster

Poster title

Applicant name

Status


1-RFC8	PREDICT A randomized investigation of a reduced prenatal dexamethasone dose to reduce virilization in female fetuses with congenital adrenal hyperplasia	Uta Neumann	Received

1-RFC5	ABOUT CARING FOR PATIENTS AND UNDERSTANDING THEIR PATHWAYS: 10 YEARS OF THE ROTTERDAM CENTRE FOR ADULTS WITH RARE GENETIC SYNDROMES	Jacqueline Goos	Received

1-RFC6	Frequency of genetic variants in a population with early-onset obesity: a single center experience	Giuseppina Rosaria Umano	Received

1-RFC12	From neurology to endocrine: Misdiagnosed MCT8 deficiency	Yasemin Denkboy Öngen	Received

1-RFC13	MRI-based radiomics of the pituitary gland is highly predictive of CentralPrecocious Puberty in girls: pilot study	Maria Elisabeth Street	Received

1-RFC10	Long-Term Endocrine Outcomes of Acute Lymphoblastic Leukemia Treatment with Special Emphasis on the Gonadal Impact	HASAN KARAKA&350;	Received

1-RFC4	Screening for Adrenal Insufficiency in Children by Home Waking Salivary Cortisone testing	Jessica Craig	Received

1-RFC14	The LIFE-MILCH project: preliminary data from the risk assessment model of exposure to Endocrine Disrupting Chemicals (EDCs) in mother-infant dyads during the first 3 months of life.	Beatrice Righi	Received

1-RFC7	Understanding the molecular basis of short stature in Fanconi Anemia: Impact of pappalysins and stanniocalcins on IGF-I bioavailability	Beatriz Corredor	Received

1-RFC3	DNA Methylation profiles in girls with anorexia nervosa and amenorrhea: a pilot study	Anna Grandone	Received

1-RFC1	Perceptions and Experiences of PDSNs on Different Hybrid Closed Loop Systems (HCLS) across Wales	Nway Nway Htun Kyi	Received

1-P3	Growth and Final Adult Height Outcomes in Pediatric Patients with Salt-Wasting Congenital Adrenal Hyperplasia	FAWZIYA ALYAFEI	Received

1-T	Genetic and Nutritional Influences on Growth: A Case of PAPPA2-Related Growth Disorder in a Pediatric Patient.	fawziya alyafei	Received

2-RFC6	Genetic Diagnostic Yield of Obesity	Antje Garten	Received

2-P2	ESPE School: Sharing Knowledge to Save Lives - Developing and Standardizing Education for Healthcare Providers and Families with Children with Adrenal Insufficiency in Kazakhstan	Aliya Zetova	Received

2-P1	Reciprocal regulation of 11b-HSD1/2 correlates initial glucocorticoids responsiveness in childhood acute lymphoblastic leukemia	SHUJI/S SAI	Received

2-RFC4	Salivary cortisol and cortisone is related to age	Sarah McNally	Received

2-RFC2	Microarchitectural Alterations in Children with Rheumatological conditions on Long-term Glucocorticoid Treatment	Joanna Tung	Received

2-RFC5	The development and validation of Bone age-guided Interpretation of Growth (BIG), a web-based tool for the guidance of evaluation of children and adolescents with growth disorders.	Vibha yadav	Received

2-RFC3	Results from a targeted hypopituitarism gene panel in patients with variable congenital hypopituitarism identifies variants in known and novel candidate genes.	Louise Gregory	Received

2-RFC15	Study on effects of poly- and perfluoroalkyl substances on hormones in girls with central precocious puberty	Yan Li	Received

2-T	Comprehensive Evaluation of Anastrozole in Pediatric Height Management and Bone Health A Real World Data	reham Ghanim	Received

2-RFC12	Prevalence and etiology of thyroid disorders and Characteristic of thyroid function tests in preterm infants	Pichaya Vathanasakpuban	Received

2-P3	A case of suspected Pigmented primary nodular adrenocortical disease with a Tanner stage inconsistent with testosterone levels	Eri Tanimoto	Received

3-RFC11	Ultrasound evaluation of kidney and liver involvement in Bardet-Biedl syndrome	Metin Cetiner	Received

3-T	Development and Validation of DSD Interpreter, a Mobile Application-Based Tool for Point-of-Care evaluation of Children with Atypical Genitalia.	Dhvani Raithatha	Received

3-P3	Towards Universal Congenital Adrenal Hyperplasia Newborn Screening in Indonesia: Knowledge, Perspectives and Experience of Pediatric Residents and Pediatricians	Agustini Utari	Received

3-RFC6	Identification and clinical characterization of new patients with novel monogenic agouti-like obesity trait	Eric Wenzel	Received

3-RFC10	Anthropometric changes in survivors of childhood acute lymphoblastic leukemia treated on the Italian Association of Pediatric Hematology and Oncology protocols without radiotherapy in the last two decades: preliminary data from an Italian tertiary center.	Patrizia Bruzzi	Received

3-RFC14	Complex Glycerol Kinase Deficiency: four new cases and a review of the literature	Fengxue Wang	Received

3-P1	Insulin-induced copeptin response in children and adolescents to diagnose arginine vasopressin deficiency*	Sebastian Gippert	Received

3-RFC9	Nanoencapsulated Curcumin-Piperine Complex: A Breakthrough in Targeting CYP17A1 for Managing Androgen Excess in Adolescents with PCOS.	Jibira Yakubu	Received

3-RFC7	Incidence of false positive results of growth hormone stimulation tests in children with short stature from theoretical background to clinical approach	Joanna Smyczynska	Received

3-RFC12	Mechanisms and natural history of pituitary resistance to exogenous thyroxine in children with congenital hypothyroidism	Jamala Mammadova	Received

3-RFC4	Differences and similarities in salivary diurnal adrenal hormones in monozygotic twins with intra-twin birthweight-differences	Thea Roedig	Received

3-P2	The Impact of the COVID-19 Pandemic on Patients with Adrenal insufficiency	Sujin Kim	Received

4-T	More than 15 years of activity of the Ghent pediatric gender service: trends in referrals and medical steps.	Silvia Ciancia	Received

4-RFC11	Association of whole blood amino acid and acylcarnitine metabolome with anthropometry and IGF1 serum levels in healthy children and adolescents	Antje Garten	Received

4-RFC4	Serum cortisol correlates strongly with salivary cortisol and cortisone in girls and boys, and across all ages	Olivia Buckingham-Woodhouse	Received

4-RFC10	Manifestation of PTEN and MUTYH gene mutations: A Case Report	Ruta Navardauskaite	Received

4-P3	Bridging Gaps in Congenital Adrenal Hyperplasia Care: Insights from General Practitioners Knowledge, Attitudes, and Experiences in Indonesia	Helena Arnetta Puteri	Received

4-RFC7	Use of iSYS-IDS IGF1-Assay Normative Data as a STANDARD in the Diagnosis of Pediatric Growth Hormone Deficiency	ADEL DJERMANE	Received

4-P2	Pitfalls in diagnosis of Congenital Adrenal Hyperplasia due to 3beta-hydroxysteroid dehydrogenase type 2 (HSD3B2) deficiency A Problem of Assay Interference	Chamila Balagamage	Received

4-RFC12	Establishing Outcomes and Management of Mild Neonatal Hyperthyrotropinaemia, a Retrospective Multi-Centre Review	Naomi Howard-James	Received

4-RFC9	Testicular function in prepubertal boys with haematological malignancies during and post chemotherapy: a prospective, longitudinal study	Jimena C. Lopez Dacal	Received

4-RFC15	Autoimmunity in children with type 1 diabetes in association with the COVID_19 pandemic - results from the prospective DPV Registry	Claudia Boettcher	Received

4-RFC5	Analysis of growth patterns in Klinefelter syndrome using the QEPS growth model	Anton Holmgren	Received

4-RFC3	Serum DLK1 During Minipuberty and Pubertal Transition in Healthy Girls and in Girls with Precocious Puberty	Lea Vilmann	Received

4-RFC1	Children born small for gestational age (SGA) under growth hormone treatment have similarly impaired glucose-insulin metabolism as children with obesity	Robert Stein	Received

4-RFC14	Neurodevelopmental response to nifedipine treatment in an infant with Congenital Hyperinsulinism due to de novo gain-of-function CACNA1D variant.	Divya Pujari	Received

5-RFC15	Prevalence and management of modifiable cardiovascular risk factors among adolescents and young adults with type 1 diabetes a cross-sectional analysis from the Diabetes Prospective Follow-Up Registry DPV	Alena Welters	Received

5-RFC5	Searching for associated dysmorphic and cardiac abnormalities in youth tall basketball players	Katerina Gregorova	Received

5-P3	46,XX DSD secondary to Maternal Adrenocortical Tumor	ANJU JACOB	Received

5-P1	Evaluation of 2 years second-tier testing for the screening on congenital adrenal hyperplasia (CAH)	Anouk Olthof	Received

5-RFC13	The Development and Validation of Bone-age guided Interpretation of Puberty, a web-based tool for guidance of pubertal disorders	Dhvani Raithatha	Received

5-RFC11	Hepatic lipogenesis increases FGF21 in children/adolescents with obesity.	Anita Morandi	Received

5-RFC14	The utility of ketones in screening for congenital hyperinsulinism: a retrospective evaluation.	Jennifer Whitehead	Received

5-RFC8	Mitochondrial Nicotinamide Nucleotide Transidrogenase (NNT) and NNT-AS1 impairment is associated with worse outcomes in patients with adrenocortical tumors	Aline Faccioli Bodoni	Received

5-RFC3	Long-Term Health Outcomes of Delayed Puberty in Males: A Comprehensive Population-Based Study	Maria Lodefalk	Received

5-RFC9	Reevaluating Guidelines for Primary Ovarian Insufficiency Workup: Is It Time for a Change?	Noah Gruber	Received

5-RFC2	Prediction of residual growth potential in girls reached menarche by linear regression modeling based on the radiomics features extracted by knee DR images and clinical characteristics	Xueqiong Xu	Received

5-RFC6	GRB10 METHYLATION IN UMBILICAL CORD ASSOCIATES POSTNATALLY WITH OBESITY IN HEALTHY CHILDREN	Abel López-Bermejo	Received

5-P2	Pharmacological therapy of adrenal hypercortisolism in a boy with suspected isolated micronodular adrenal hyperplasia (iMAD) due to a mutation in the PDE11A gene	Michaela Marx	Received

5-RFC7	HEALTH-RELATED QUALITY OF LIFE AT MID-PUBERTY IN ADOLESCENTS WITH IDIOPATHIC ISOLATED GROWTH HORMONE DEFICIENCY	Joeri Vliegenthart	Received

5-T	Endocrine and metabolic complications after solid organ transplantation in childhood and adolescents	Ji-Hee Yoon	Received

6-RFC7	Big data as a strategy in the development of population auxological studies	Ignacio Diez	Received

6-P3	Induced Adrenal Insufficiency: Case series	ADEL DJERMANE	Received

6-RFC15	Macrophage switch and iron metabolism regulation by Burosumab in XLH pediatric patients: implications in inflammation and pain modulation.	Anna Grandone	Received

6-P1	Impact of Fludrocortisone on Blood Pressure in Young Children Under 5 with CAH in the I-CAH Registry: Autoregressive Causal Inference Analysis	Neil Lawrence	Received

6-RFC13	Hypogonadism hyperprolactinemia-related and its treatment in three patients with inherited disorders of biogenic amine metabolism	Sara Soldovieri	Received

6-RFC10	Different Faces of Carney Complex: Report of Three Cases	Ilayda Altun	Received

6-RFC11	Pten knockout in osteoprogenitor cells leads to loss of adipose tissue	Florentien Kolbig	Received

6-RFC1	METABOLIC DYSFUNCTION-ASSOCIATED STEATOTIC LIVER DISEASE AND ITS ASSOCIATION WITH GLYCEMIC CONTROL METRICS IN CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES: AN EXPLORATORY STUDY	Valentina Mancioppi	Received

6-RFC8	Prospective evaluation of urinary outcome after partial urogenital sinus mobilization (PUM) for toilet trained female patients with classic congenital adrenal hyperplasia (CAH).	Noha Aly	Received

6-RFC14	Utility of Continuous Glucose Monitoring in hospital monitoring of patients with Hyperinsulinism	Shamani De Silva	Received

6-T	Gonadal function in patients with germline variants of WT1 : results from the French GONADVENIRs retrospective study.	Morgane Carré Lecoindre	Received

6-RFC2	Comparison of two automated bone age evaluation methods in pediatric patients with growth and puberty disorders	Inge Lore Ruiz Arana	Received

6-RFC6	POTENTIAL ROLE OF ASPG METHYLATION AS A BIOMARKER OF CHILDHOOD OBESITY	Ariadna Gomez	Received

7-T	Long-read sequencing analysis in two Beckwith-Wiedemann syndrome families caused by defects of OCT4/SOX2 binding site	Hayate Masubuchi	Received

7-P1	Variation in Blood Pressure in Young Adults with 21a-Hydroxylase Deficiency: Longitudinal Multilevel Modelling of Data from the I-CAH Registry	Neil Lawrence	Received

7-P2	ESPE Caucasus&Central Asia School (C&CAS) Sharing Knowledge for Saving Patients Lives:Organizing pediatric endocrinology care for patients with adrenal insufficiency in Armenia.	Sona Samvelyan	Received

8-P1	Leptin and adiponectin are associated with the glucocorticoid dose and androgen concentrations in children and young persons with congenital adrenal hyperplasia: data from the CAH-UK cohort.	Irina A Bacila	Received

8-T	Predicting the risk of fragility fractures in childhood hematologic cancer survivors	Luminita-Nicoleta Cima	Received

8-P3	RARE PRESENTATION OF CATECHOLAMINE-SECRETING TUMOR IN AN INFANT: EXCESSIVE THIRST AND POLYDIPSIA	Sebla Güne&351;	Received

9-P1	Exploring the Long-Term Consequences of Congenital Adrenal Hyperplasia: First Study of Testicular Adrenal Rest Tumors Profile in Indonesia	Agustini Utari	Received

9-T	Differential microRNA Expression Profiles in Girls with Central Precocious Puberty and Premature Thelarche	Hye Jin Lee	Received

9-P3	Early Diagnosis and Management of Aldosterone Synthase Deficiency in Infancy: A Case Report	Bogdan Mihai Pascu	Received

10-P2	Early Diagnosis of Adrenoleukodystrophy in Two Siblings	Kiymet Karagoz	Received

10-T	Phenotypic and genotypic characterization and long-term follow-up of patients with thyroid hormone resistance	Tessa Van der Auwera	Received

10-P1	Causality between Sex Hormones and Bone Mineral Density in Childhood: Age- and Tanner stage-matched Sex Hormone Level May be an Early Interpreter of Pediatric Bone Fragility	Sung Eun Kim	Received

11-P3	PRIMARY ADRENAL INSUFFICIENCY: CASUISTRY OF A THIRD LEVEL HOSPITAL	Cristina Aguilar Riera	Received

11-P2	Iatrogenic adrenal insufficiency a single centre response to increasing awareness and instituting management in non-endocrine specialities.	Sally Tollerfield	Received

11-T	Postnatal detection of sex chromosome abnormalities by quantitative fluorescence polymerase chain reaction potential for newborn screening	Camilla Mains Balle	Received

12-P1	X-linked hypophosphatemia caused by a novel deep intronic variant in the PHEX gene	Dr. Angela Huebner	Received

12-T	Investigating the Effects of Familial Mediterranean Fever on Growth and Puberty: Does the Duration of Puberty Change?	Ozge Bayrak Demirel	Received

12-P2	Central adrenal assessment in a group of prepuberal Prader Willi Syndrome patients in a tertiary center	Elisa Vaiani	Received

12-P3	An unusual case of remission of clinically overt autoimmune Addisons disease in a Pakistani girl.	Kashan Arshad	Received

13-P3	Focus on the project: ITASAG24, observational, multicenter study comparing Italian regions with and without neonatal screening for Congenital Adrenal Hyperplasia	Laura Corbelli	Received

14-T	ATA-Pediatric low-risk differentiated thyroid carcinoma (PLR-DTC): starting to withhold radioiodine therapy (RAIT)	PATRICIA PAPENDIECK	Received

14-P2	Clinical characteristics of rare forms of paediatric congenital adrenal hyperplasia (CAH) in a single tertiary centre	Meera Shaunak	Received

14-P3	Combined Therapy with GnRH Analogue, Aromatase Inhibitor, and Growth Hormone on Adult Height in Non-Classical Congenital Adrenal Hyperplasia: A Case Report	Sabina Sharifova Mirzayev	Received

15-T	Alterations in BMI and Body Composition Twelve Months After Cessation of Growth Hormone Therapy in Adolescents with Prader-Willi Syndrome (PWS)	Constanze Lämmer	Received

15-P2	Premature Adrenarche, Body Composition and Metabolic Dysfunction Characterisation of a Pilot Cohort	wogud Ben Said	Received

15-P3	Cushings disease in pediatrics. Case report.	Consuelo Pino	Received

15-P1	Adipokines level and vertebral fracture in children and adolescent with systemic lupus erythematous receiving glucocorticoid therapy	Voraluck Phatarakijnirund	Received

16-T	The importance of genetic diagnosis in obesity - leptin-melanocortin pathway and beyond.	Robert ket	Received

16-P2	THE CHALLENGE OF DIAGNOSIS AND MANAGEMENT OF MICRONODULAR ADRENOCORTICAL DISEASE IN A 7-YEAR OLD GIRL WITH CYCLIC CUSHINGS SYNDROME: A CASE REPORT	Olimpia Alice Manzardo	Received

16-P3	ADRENAL INSUFFICIENCY DUE TO BILATERAL ADRENAL HAEMORRHAGE IN A NEWBORN AFTER SUFFERING PERINATAL ASPHYXIA: A CASE REPORT	Olimpia Alice Manzardo	Received

17-T	Burden of disease across age groups in individuals with hereditary hypophosphatemia a retrospective Danish register study	Clara Utley	Received

17-P1	New clinical phenotypes associated with ALPL mutations	Mariam Farman	Received

17-P3	Surgical interventions in girls with congenital adrenal hyperplasia Experience from a low middle income country A preliminary report.	Thabitha Hoole	Received

17-P2	17OHP and cortisol day curve profiles for children using hard-capsule modified release hydrocortisone as compared with immediate release hydrocortisone.	Grace Petkovic	Received

18-P3	Nephrocalcinosis in one pediatric patient with Congenital Hyperplasia. Case report.	Consuelo Pino	Received

18-P2	Determination of Anti-Müllerian Hormone and Inhibin B Reference Ranges According to Pubertal Stages in Children and Adolescent Girls	Ozge Kaynar Sidimi	Received

18-P1	Vosoritide therapy in 16 young children with achondroplasia: a retrospective study	Natsuho Adachi	Received

18-T	DNA methylation level at five specific CG-sites within TRAK1 correlates with the neurocognitive profile in individuals with Klinefelter syndrome.	Helene Bandsholm Leere Tallaksen	Received

19-T	Ultrasonographic Evaluation of Ovarian and Uterine Morphology in Minipuberty and Associations with Reproductive Hormones: A COPANA Cohort Study of 302 infant girls.	Margit Bistrup Fischer	Received

19-P1	Autosomal Dominant Hypocalcemia type 1 (ADH 1) with hypercalciuria due to CASR Ser820Phe mutation: a case report	Emanuela Pignatone	Received

19-P3	A case of primary amenorrhea in a 17-year-old patient	Kamila Szeliga	Received

19-P2	Metabolic risk factors in children with Premature Adrenarche a systematic review and meta-analysis	wogud Ben Said	Received

20-T	Real World Effectiveness of Vosoritide in 165 Children with Achondroplasia Data from a Multicenter European Registry	Katja Wechsung	Received

20-P1	Cross-talk between mechanical loading and longitudinal bone growth under chronic inflammation	Tim Aeppli	Received

20-P3	A case of Familial Glucocorticoid Deficiency	Francisco Branco Caetano	Received

21-P2	Should we routinely screen for adrenal rests in Congenital Adrenal hyperplasia?	Abeer Alkhalaf	Received

21-P1	A population preventive study of early detection of type 1 diabetes in asymptomatic children in the North-East region of Poland	Artur Bossowski	Received

21-P3	Pitfalls of Diagnosing 11-OHD in Limited Settings	Sare Kaygusuz	Received

22-P3	X-LINKED ADRENOLEUKODYSTROPHY: A CASE SERIES	Sibel Tugce Aygün	Received

22-P1	CLINICAL AND MOLECULAR SPECTRUM OF POLYCYSTIC KIDNEY SYNDROME AND DIABETES DUE TOMUTATIONS IN HNF-1B	Luis Salamanca Fresno	Received

22-P2	Severe Adrenocortical Carcinoma Presentation with Vena Cava Involvement in a 1-Year-Old Boy: A Case Presentation and Management Considerations	Dimitrije Cvetkovic	Received

23-P2	Adrenal Lesions Evaluated in A Pediatric Endocrinology Department	Selen Hürmüzlü Közler	Received

23-P3	Case report for a 15-year-old black girl with genu valgus and abnormal gait.	fawziya alyafei	Received

24-P3	An Update on Biochemical Findings for Stages of Nutritional Rickets	Huseyin Anil Korkmaz	Received

24-P2	Genotype-Phenotype correlations in three patients with CYP21A2 picked up by 17- ? OHP screening	Kalina Mihova	Received

24-P1	Associations between arterial stiffness and metabolic target in children and adolescents with type 1 diabetes treated in a modern setting	Julie Agner Damm	Received

25-P2	X-linked congenital adrenal hypoplasia due to a novel mutation in NR0B1 gene	Zdravka Todorova	Received

26-P1	Exercise induced hyperinsulinism: A rare cause of recurrent hypoglycaemia	Sarita Bosco	Received

26-P2	Bisphosphonate Therapy in a Pediatric Case Series with Monostotic Form of Fibrous Dysplasia: A Single-Center Retrospective Analysis of Efficacy and Safety	Nikola Ilic	Received

27-P2	Infantile hypercalcemia with CYP24A1 variant triggered by fortified milk	Sota Iwafuchi	Received

27-P3	Insight Bone Metabolism Disorders in Pediatric Patients: A Tertiary Hospital Study	giorgiana flavia brad	Received

27-P1	Insights into the Application of Molecular Genetics for Early Onset Diabetes Mellitus in a Prospective Pediatric Study	Yoo-Mi Kim	Received

28-P2	HDR syndrome due to a new mutation in the GATA3 gene	Zeynep Donbaloglu	Received

28-P3	Incomplete penetrance and Variable Expressivity in Monogenic Diabetes	Shiga Chirayath	Received

28-P1	Role of urinary tumor necrosis factor-alpha and transferrin in the diagnosis of diabetic nephropathy in pediatric patients with type 1 diabetes mellitus.	Iskra Modeva	Received

29-P1	Wolcott-Rallison Syndrome: A Case Report of a Novel Mutation	Kashan Arshad	Received

29-P3	Rare combinations: Loeys-Dietz Syndrome Type 2 with Type 1 Diabetes mellitus and Loeys-Dietz Syndrome Type 4 with congenital hypothyroidism due to thyroid hypoplasia.	Platonas Karatsiolis	Received

29-P2	Vitamin D dependent rickets Type 2A: A case series of two siblings with novel mutation in vitamin D receptors responded to high dose oral calcium and calcitriol.	Noor-ul-ain Mehak	Received

30-P3	Red flag for the diagnosis of non-nutritional rickets: experience of a single centre in Southern Italy	Fabio Toscano	Received

30-P2	Investigation of GNAS Gene Mutation and Clinical Correlations in Patients Followed with the Diagnosis of Pseudohypoparathyroidism	Esra Deniz PAPATYA AKIR	Received

30-P1	The Impact of Sleep Quality and Metabolic Control in Children with Type 1 Diabetes: a Prospective Cohort Study	Dina Bashammakh	Received

31-P1	Rare forms of (non)syndromic monogenic diabetes in the Czech registry of patients susceptible for monogenic diabetes	Stepanka Pruhova	Received

31-P2	Bisphosphonates : A promising treatment for osteolytic lesion in Langerhans cell histiocytosis	Cindy Ho	Received

31-P3	BUROSUMAB AS A TREATMENT FOR X-HYPOSPHOSPHAMETIC RICKETS:REPORT OF TWO CASES	Panagiota Georgia Maltezou	Received

32-P3	Growth hormone treatment in a case of cleidocranial dysplasia with growth hormone deficiency	Jeesuk Yu	Received

32-P2	A rare presentation of parathyroid adenoma as bilateral genu valgum in an adolescent Pakistani girl.	Sommayya Aftab	Received

32-P1	Factors Associated with Pump Set Occlusion	Elif Tuge Tunca Küükali	Received

33-P1	A Case of Mild Clinical Course MODY9	Agh Akin	Received

33-P3	Rare Presentation of Rare Disease: Case report of Prenatal onset Hypophosphatasia	Hanan AL Azkawi	Received

33-P2	Dysplasia Epiphysealis Hemimelica combined with Familial Hypocalciuric Hypercalcemia can the calcium-sensing receptor have a role in expansive bone lesions?	Barbara Aoto	Received

34-P1	SEXUAL KNOWLEDGE AND CONTRACEPTIVE USE IN ADOLESCENTS WITH TYPE 1 DIABETES IN COMPARISON WITH THEIR HEALTHY PEERS	Betina Kandyla	Received

34-P3	Evaluation of Bone Health in Children Treated for Acute Lymphoblastic Leukemia*	Rabia oban	Received

34-P2	Persistent Hypocalcemia In a Pakistani Infant: A Rare Activating CaSRMutation	Dr Syed Saddam Hussain	Received

35-P1	Diabetes Mellitus in Woodhouse -Sakati syndrome	Rasha Amin	Received

35-P2	Tibial-tubercle avulsion and patellar-tendon rupture in an adolescent with osteogenesis imperfecta	Kübra Sen Küük	Received

35-P3	Micronutrients, especially zinc, are essential for the proper growth and development of children	Ana kokhreidze	Received

36-P3	A 5-year-old girl with severe nutritional rickets mimicking hypophosphatemic rickets (XLH)	Stefano Zucchini	Received

36-P2	KIF22 Mutation with Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type 2 (SEMDJL2)	Betül Liv anga	Received

36-P1	HAIR PROTEOMICS PROFILE IN GIRLS WITH NEWLY-DIAGNOSED TYPE 1 DIABETES MELLITUS	Nicolas Nicolaides	Received

37-P1	INFLUENCE OF TYPE 1 DIABETES ON AGE OF MENARCHE IN GIRLS WITH TYPE 1 DIABETES	Maja Vinkovic	Received

37-P2	Vosoritide Therapy in Children with Achondroplasia: Single-Center Experience	Rasha Amin	Received

37-P3	A Case of Intravenous Pamidronate Treatment for Steroid-Induced Osteoporosis in a Patient with Rhematic Arthritis	Ji-Young Seo	Received

38-P2	KENNY-CAFFEY SYNDROME IN THE NEONATAL PERIOD	Júlia Galhardo	Received

38-P1	A Retrospective Analysis of Cost of Admission Care in Children with First Presentation of T1D at University Hospital Limerick: Assessing the Feasibility of Ambulatory Care	Lucy Angela Dockery	Received

39-P3	Phenotypic and Genotypic profile of VDDR type1A: An experience from West Yorkshire, UK	Sarita Bosco	Received

39-P1	The Effect of Excessive Fructose (Corn Syrup) Consumption on Insulin resistance, Lipid Profile and Lipid Peroxidation	Huseyin Anil Korkmaz	Received

39-P2	PTHLH gene mutation: A rare diagnosis of skeletal dysplasia	Samia Almalki	Received

40-P2	An adolescent health care clinic at King Abdulaziz Medical City, Jeddah, Saudi Arabia	Najya Attia	Received

40-P1	DETECTION OF RISK OF NON-ALCOHOLIC HEPATIC STEATOSIS (NASH) IN OBESE CHILDRENS POPULATION THROUGH RAPID ULTRASOUND MEASUREMENT OF PREPERITONERAL ABDOMINAL FAT AT THE BED SIDE. A NEW STRATEGY	Ignacio Diez	Received

40-P3	Genetic Rickets: Can it be that early?	Tahani Alharbi	Received

41-P1	Prediction of hepatic fibrosis using the aspartate transaminase-to-platelet ratio index in children and adolescents with non-alcoholic fatty liver disease	Eun Young Kim	Received

42-P3	Access to physiotherapy for children with Osteogenesis Imperfecta in Austria	Adalbert Raimann	Received

42-P2	THE ETIOLOGICAL DISTRIBUTION OF ELEVATED SERUM ALKALINE PHOSPHATASE LEVELS AND CHARACTERISTICS OF CHILDREN WITH TRANSIENT HYPERPHOSPHATASEMIA	&304;lkay Bahar Balaban Berber	Received

42-P1	Unravelling the relationship between Head Circumference and Melanocortin4-Receptor deficiency from infancy to adulthood: a case-control study	Eline van der Walle	Received

43-P1	BIO-STREAMS: Multi-Pillar Framework for children Anti-Obesity Behavior building on an EU biobank, Micro Moments and Mobile Recommendation Systems	Penio Kassari	Received

43-P2	The development of low selenium concentrations in children undergoing liver transplantation	KOGORO IWANAGA	Received

43-P3	About a case of Trichorhinophalangien Syndrome	nadira rouabah	Received

44-P3	Congenital hypomagnesaemia in four Algerian families the need for early diagnosis and treatment to avoid neurodevelopmental delay	Kamelia Boulesnane	Received

44-P2	Use of denosumab in aneurysmal bone cyst and giant cell tumor in a third-level pediatric center	gisela viterbo	Received

44-P1	ASSESSMENT OF METABOLOMIC-NUTRITIONAL STATUS AND CARDIOVASCULAR RISK IN ADOLESCENTS WITH ANOREXIA NERVOSA AND LOW BODY WEIGHT	Paula Sol Ventura	Received

45-P2	Hereditary hypophosphatemic rickets with hypercalciuria: a rare disorder not to be forgotten about	Matteo Pontone	Received

45-P1	EARLIE Pilot study for universal familial hypercholesterolemia screening in Luxembourgish primary school children	Marianne Becker	Received

46-P3	Parathyroid adenoma in a 12-year-old boy with incidental hypercalcemia	Nobuhiko Koga	Received

46-P1	Circulating levels of ghrelin in patients with rare diseases with intellectual disability associated with hyperphagia, and/or overweight, and/or obesity The HOGRID study	Sandy FAYE	Received

46-P2	Advanced bone age in short stature due to ACAN gene mutation: a case report.	Beatrice Righi	Received

47-P1	Sleep quality and telomere length after long-term impact of a lifestyle intervention in patients with abdominal obesity	Maria Cristina Azcona-Sanjulian	Received

47-P2	Evaluation of Pediatric Cases with ACAN Gene Variants	Aysun Ata	Received

48-P2	Two compound heterozygous variants in SLC34A1 causing idiopathic infantile hypercalcaemia (IIH) type 2 - a case report	Christin Maria Duffert	Received

48-P3	Influence of the Bacillus Calmette-Guérin vaccine on the incidence of cases of type 1 diabetes mellitus in children and adolescents in the Basque Country (last CCAA to withdraw vaccination in Spain)	Ignacio Diez	Received

48-P1	RELATIONSHIP BETWEEN SERUM AND FAECAL ZONULIN CONCENTRATION AND GLUCIDIC METABOLISM IN CHILDREN AND ADOLESCENTS WITH OBESITY	Giorgia Pepe	Received

49-P3	STUDY OF THE ELECTRICAL STABILITY OF THE HEART MUSCLE IN CHILDREN WITH TYPE I DIABETES MELLITUS	Laman Sultanova	Received

49-P1	Correlations Between Nutritional Interventions, Growth Dynamics, and IGF-1 Levels in Pediatric Populations: A Comprehensive Analysis	nada alaaraj	Received

50-P1	Genetic Variations in IGF1R and IGF1: Elucidating Their Role in Growth Disorders and Therapeutic Responsiveness	FAWZIYA ALYAFEI	Received

50-P2	Lysinuric Protein Intolerance: A Case Report of a Child Presenting with Multiple Fractures to Bone Clinic	Olivia Holland	Received

50-P3	The Effect of Continuous Glucose Monitoring Device Assistance on Glycaemic Control in Children and Adolescents with Type 1 Diabetes Following the 2023 Türkiye Earthquake Doublet: A Multicentre Study	Gürkan Tarin	Received

51-P1	The Metabolic Impacts of GH Therapy in SGA Children and Its Effects on Various Metabolic Parameters and Health Outcomes	FAWZIYA ALYAFEI	Received

51-P3	Mauriac Syndrome: A Clinical Case of a Rare Complication in Pediatric Type I Diabetes Mellitus	Warisa Uthayo	Received

52-P1	Changes in Length and Weight Standard Deviation Scores in Children with Growth Hormone Deficiency Across Various Studies	FAWZIYA ALYAFEI	Received

52-P2	Current challenges in diagnosis, treatment, and follow-up of children with parathyroid hormone dysfunction lessons learned from a cohort of children presenting with hypocalcaemia	Ana Laura Fitas	Received

53-P1	Correlation of Growth Hormone Secretion and Infantile Growth Patterns in Children Diagnosed with Growth Hormone Deficiency (GHD)	FAWZIYA ALYAFEI	Received

53-P3	Diabetic Neuropathic Cachexia and Mauriac Syndrome : A Rare Complication of Poorly Controlled Diabetes Mellitus	ADEL DJERMANE	Received

53-P2	Bone mineralization at age 5 years in very preterm vs term-born children	Demi Dorrepaal	Received

54-P1	Should MRI Be Performed on the Pituitary Gland in Short Stature Children with Peak Growth Hormone Levels Between 5 and 7 Micrograms/Liter Following Provocation Tests?	FAWZIYA ALYAFEI	Received

54-P2	The clinical burden and healthcare resource utilization among children and adolescents with osteogenesis imperfecta: an observational study using Optums de-identified Clinformatics Data Mart Database	Yasmin Lau	Received

55-P2	Bone Mineral Density in Children with Inflammatory Bowel Disease	Omneya Omar	Received

55-P1	The Relation Between Serum Glucose and Growth Hormone Concentrations During Standard Glucagon Test for GH Release in Short Stature Children	fawziya alyafei	Received

56-P3	FREQUENCY AND ASSOCIATED FACTORS OF LIPOHYPERTROPHY IN CHILDREN AND ADOLESCENT WITH TYPE 1 DIABETES IN A SINGLE TERTIARY CARE CENTRE.	Kashan Arshad	Received

56-P2	Real-world effectiveness of vosoritide in children with achondroplasia: Results from 18 months follow-up in France	Amin Ghane	Received

56-P1	BODY COMPOSITION ABNORMALITIES DURING THE TRANSITION STAGE IN MALES WITH GROWTH HORMONE DEFICIENCY (GHD) AFTER COMPLETION OF REPLACEMENT THERAPY	CARLA BOQUETE	Received

57-P2	Sleep disturbances in children and adolescents with type 1 diabetes mellitus: Prevalence, and relationship with diabetes management	Zeynep Donbaloglu	Received

57-P3	MANAGEMENT OF A CLINICAL CASE OF TYPE 1 DIABETES IN THE PRE-ASYMPTOMATIC STAGE	Zacharoula Karabouta	Received

57-P1	Long-term treatment with recombinant human growth hormone in pediatric patients influences but does not destroy stem cells circulating in peripheral blood	Anna W&281;drychowicz	Received

58-P2	The Relationship of Serum Diabetes Antibodies with the Development of Early Diabetic Retinopathy Findings in Children with Type 1 Diabetes Mellitus	Huseyin Anil Korkmaz	Received

58-P3	Relationship between body mass index and metabolic control in patients with type 1 diabetes mellitus	Senay Savas Erdeve	Received

58-P1	Somapacitan is Effective and Well Tolerated in Chinese Children with GHD: 52-week Results from the Randomized Phase 3 REAL6 Trial	Junfen Fu	Received

59-P2	Impact of Telemonitoring on Glycemic Control in Pediatric Patients with Type 1 Diabetes Mellitus	Radwa Shamma	Received

59-P1	Near adult height in prepubertal children treated with growth hormone: differences between definite growth hormone deficiency (dGHD), short stature unresponsive to stimulation tests (SUS) and idiopathic short stature (ISS)	Gianluca Tornese	Received

59-P3	Comparative characterization of prediabetes and diabetes mellitus type 2 in adolescents with obesity	Nadezda Minkova	Received

60-P1	Big data tools for assessing the nutritional situation of a pediatric population : did the prevalence of obesity change pre- and post-pandemic?	Ignacio Diez	Received

60-P3	Evaluating the diagnostic utility of Autoantibodies in Korean pediatric diabetes patient	Eun Young Joo	Received

60-P2	THE INCIDENCE OF TYPE 1 DIABETES AMONG ESTONIAN CHILDREN IN 2007-2022 IN COMPARISON WITH THE DATA FROM 1983 TO 2006 AND THE IMPACT OF THE COVID-19 PANDEMIC.	Vallo Tillmann	Received

61-P1	Comparison of the diagnostic yield of whole exome sequencing (WES) and targeted panel sequencing for children with idiopathic short stature (ISS)	Laurana Cellin	Received

61-P2	A Novel Disease-causing Variant of INS-MODY with a Unique Phenotype.	Cherie Chua	Received

62-P3	Severe hypertriglyceridaemia and lipaemia retinalis in a child presenting with diabetic ketoacidosis	Kathryn Kimber	Received

62-P2	Founder WSF1 Mutation Causing Wolfram Syndrome in the Druze Population in Israel	Inbal Halabi	Received

63-P1	Long-term effectiveness and safety data from the Global Increlex Registry in patients treated with rhIGF-1: Subgroup analysis of naïve prepubertal patients and patients with Laron syndrome	Orla Woodward	Received

63-P2	The frequency of anemia and the evaluation of related factors in patients with type 1 diabetes mellitus	Esra Deniz PAPATYA AKIR	Received

63-P3	Diabetes Mellitus in children with pancreatitis. Report of three cases	Consuelo Pino	Received

64-P3	A case of insulin autoimmune syndrome onset at the age of 3	Yuan Ding	Received

64-P2	AUTOMATED INSULIN DELIVERY SYSTEMS: ARE THEY ALL THE SAME? FOLLOW-UP OUTCOMES OF TWO HCLS IN YOUTHS WITH TYPE 1 DIABETES: A 2-YEAR REAL-LIFE BASED STUDY.	Laura Sayol-Torres	Received

64-P1	Osteocalcin in infancy and early childhood correlates to growth and body composition: A longitudinal birth cohort study	Sara Berggren	Received

65-P1	Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader-Willi syndrome	Julie CORTADELLAS	Received

65-P3	Clinical characteristics and immunologic analysis of children with type 1 diabetes mellitus	Ding Yu	Received

65-P2	DIABETES MELLITUS, MACROCYTOSIS AND SKIN PIGMENTATION DISORDER IN A CHILD WITH LARGE-SCALE mtDNA DELETION	Duje Braovac	Received

66-P2	Genetic analysis and treatment of congenital hyperinsulinemic hypoglycemia: A single centers experience	Jaeeun Chung	Received

66-P1	Neutrophil-driven inflammatory stress in Turner syndrome	Lukas Ridder	Received

66-P3	An Audit Evaluating Omnipod 5 usage in Patients Under the Care of the Paediatric Diabetes Team at Wythenshawe Hospital	Rachael OBrien	Received

67-P2	Clinical Outcomes with MiniMedTM 780G Advanced Hybrid Closed-Loop Therapy In Children 7 years with Type 1 Diabetes	Nihal Gül Uslu	Received

67-P1	Study of genetic variability in a cohort of familial growth retardation	LAMBERT ANNE SOPHIE	Received

68-P3	early onset Thiamine Responsive Megaloblastic Anemia (TRMA), diabetes mellitus and sensorineural hearing loss, in 7 month infant, case report.	Maysa Saleh	Received

68-P1	Impact of Idiopathic Short Stature (ISS) on childrens well-being.	Anders Juul	Received

69-P2	Venous Sodium, Potassium, and Glucose Results on Rapid Arterial Blood Gas Analyzer in Children with Diabetic Ketoacidosis: Are the Values Comparable with Results Obtained from the Central Laboratory?	Sebla Güne&351;	Received

69-P1	Hormonal markers of ovarian function and their role in predicting reproductive lifespan in girls with Turner syndrome	Sanne van der Coelen	Received

70-P1	Two Cases of Type I Sialidosis and Literature Review	Yuan Ding	Received

70-P3	A Rare Case of Neurofibromatosis Type 1 in a Child with Diabetes Mellitus Type 1	Sokratis Katsoudas	Received

70-P2	Efficacy of Advanced Hybrid Closed-Loop System Medtronic MiniMed 780G in Japanese children with type 1 diabetes mellitus (T1DM)	Nagisa Ujita	Received

71-P2	Severe Acute Kidney Injury in an Adolescent with Diabetic Ketoacidosis	Kübra Sen Küük	Received

71-P1	Endocrine and metabolic comorbidities in juvenile-onset systemic lupus erythematosus	Su Jin Park	Received

72-P3	Cystic fibrosis-related diabetes. Report of two cases.	Consuelo Pino	Received

72-P1	Serum nesfatin-1 and GLP-1 concentrations in adolescent patients with anorexia nervosa/obesity.	Malgorzata Blaska	Received

72-P2	Neonatal Diabetes, Thrombocytopenia, and Atopic Dermatitis: A Diagnostic Challenge of IPEX Syndrome	Gizem Bakir	Received

73-P3	Recommendations for screening and prevention of bone disorders in children and adolescents with diabetes mellitus type 1	Olga Slavcheva-Prodanova	Received

73-P2	Neonatal Diabetes Due to Insulin Gene Mutation	Betül Liv anga	Received

75-P1	Endocrine Complications in Childhood Primary Brain Tumor Survivors: A Single Center Study	Nuanpan Chooprasertsuk	Received

75-P2	Rabson-Mendenhall Syndrome: Clinical presentation , genotype and management in a cohort of Sudanese children	Jouyriah Mohmmed	Received

76-P3	THE AWARENESS OF TEACHERS AND MEDICAL SCHOOL WORKERS REGARDING DIABETES IN CHILDREN	Viktoriya Furdela	Received

76-P1	The Significance of Clinical Examination in Diagnosing Genetic Diseases: An Infant with Williams-Beuren Syndrome	Sokratis Katsoudas	Received

77-P3	Modified Diabetic Ketoacidosis Protocol - 12-Year Treatment Experience	Deniz Özalp K&305;z&305;lay	Received

77-P2	Congenital Generalized Lipodystrophy in Down Syndrome patient	Andrea Soledad Reinoso	Received

77-P1	An atypical presentation of McCune Albright syndrome	Nicolas Bonnet	Received

78-P3	Severe case of Obesity and Type 2 Diabetes where to go when nothing seems to help?	Eleanor Crawley	Received

78-P1	The Endocrine Chameleon: Expanding the phenotype of Pseudohypoparathyroidism 1A in infancy A Case Series	Martin Munteanu	Received

79-P1	Clinical Characteristics and Management Outcomes in Girls with McCune-Albright Syndrome: An Experience from a Tertiary Center	Prapai Prapai Dejkhamron	Received

79-P3	COMPARATION BETWEEN 2 SISTEMS OF AUTOMATED INSULIN DELIVERY	AINA VALLS	Received

80-P3	Case Series of Five Children withThiamine-Responsive Megaloblastic Anemia in the PakistaniPopulation, a Rare Form of Monogenic Diabetes Mellitus.	Kashan Arshad	Received

80-P2	INFLUENCE OF SARS-COV-2 VIRUS ON INITIAL MANIFESTATION OF TYPE 1 DIABETES IN CHILDREN: NATIONAL DATA FROM LATVIA	Lizete Braivo	Received

80-P1	A 12-month, Open-Label, Single-Arm, Phase 3 Trial of the Efficacy and Safety of Triptorelin 6-Month Formulation in Chinese Children with Central Precocious Puberty	Amie Lochrie	Received

81-P3	A Case of Stress Hyperglycaemia with Ketoacidosis Diagnostic Dilemma	Evelyn Flynn	Received

81-P2	Sweet lies detector; Factitious Diabetes Mellitus as a rare presentation of Munchausen by Proxy syndrome	Mina Koutrouli	Received

82-P1	Comparative Analysis of a-Klotho Levels for the Diagnosis of Central Precocious Puberty (CPP) in Children: A Gender-Specific Study	&44221;&55148; &51060;	Received

82-P3	INCIDENCE OF NEW ONSET TYPE 1 DIABETES IN CHILDREN DURING THE COVID-19 GLOBAL PANDEMIC	Lobanov Michail	Received

83-P1	Frequency and phenotypic characteristics of copy number variations in patients with Kallmann syndrome and normosmic isolated hypogonadotropic hypogonadism	Dohyung Kim	Received

83-P3	The Relation between Obesity and Thyroid Function in Children and Adolescents	FAWZIYA ALYAFEI	Received

84-P3	Regulated sports activity is a greater protective factor for obesity than lunch at school, even in a pandemic.	Ignacio Diez	Received

84-P2	Endocrine Evaluation in Patients with Cystic Fibrosis: A Retrospective Study from Single Tertiary Center	Mert Uar	Received

84-P1	Use of the arginine-stimulated copeptin test in paediatric polyuria-polydipsia syndrome: experience with eleven patients	GONZÁLEZ-LLORENS NÚRIA	Received

85-P2	Clinical Characteristics and follow-up of Type 2 Diabetes in Children and Adolescents: A Single Center Experience	didem helvac&305;o&287;lu	Received

85-P3	A novel GPIHBP1 mutation of chylomicronemia syndrome: A case report:	abdullah alshahrany	Received

86-P3	SETMELANOTIDE AS TREATMENT FOR OBESITY DUE TO LEPTIN RECEPTOR (LEPR) DEFICIENCY IN A CHILD UNDER 6 YEARS OF AGE	Ana-Belen Ariza-Jimenez	Received

86-P2	ENDOTYPES IN DIABETES, DIFFERENT DIABETES, DIFFERENT MANAGEMENT?	Marta Murillo	Received

86-P1	Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients	Masayo Kagami	Received

87-P1	Phenotypic characteristic of a large cohort of pediatrics Argentine patients with PSIS. High Prevalence of Mutations in ROBO1 gene	María Isabel Di Palma	Received

87-P3	Family-Based Intervention for Overweight Children: Links Between Parental Health Attitudes, Behaviors, and Childrens Success	keren Shechter Refael	Received

88-P3	THE EFFECT OF BREASTFEEDING DURATION ON BODY MASS INDEX IN CHILDREN: WHAT IS THE SITUATION IN AZERBAIJAN CHILDREN?	Leman Sultanova	Received

88-P2	Effectiveness of Different Insulin Delivery Systems Among Preschool Children with Type 1 Diabetes	Lorena Matonti	Received

88-P1	Hypopituitarism following traumatic brain injury in children and adolescents - Long-term outcome study in a prospective patient cohort (2017-2023)	Irena Drozd	Received

89-P1	ORGANOKINES AND LIVER ENZYMES IN ADOLESCENT GIRLS WITH POLYCYSTIC OVARY SYNDROME DURING RANDOMIZED TREATMENTS	Cristina Garcia-Beltran	Received

90-P1	Decreased serum DHEAS to cortisol ratio in adolescents evaluated for gender dysphoria	Gianluca Tornese	Received

90-P2	Type 1 diabetes incidence in children aged under 15 years living in Ireland during 2022	edna roche	Received

91-P2	Prevalence, clinical, immunological and biochemical characteristics of children with Familial T1D in Kuwait	Dalia M Al-Abdulrazzaq	Received

91-P1	Serum steroid metabolite profiling by LC-MS/MS in two phenotypic male patients with HSD17B3 deficiency: implications for hormonal diagnosis	Yohei Masunaga	Received

92-P1	Phenotypic spectrum of WT1 gene variants in DSD	Mariana Costanzo	Received

92-P3	Obesity in children from 5 to 19 years old at the Vietnam Northern referral center	Khanh Nguyen Ngoc	Received

92-P2	Can asprosin be used as a diagnostic biomarker for non-alcoholic fatty liver disease in obese children?	Zeynep Donbaloglu	Received

93-P3	Exploring leptin dysfunction in severe early-onset obesity: implications for pediatric health a preliminary report	Sabina Galiniak	Received

93-P1	EuRRECa Core Registry: results from the Gender Incongruence module	Silvia Ciancia	Received

93-P2	PREVALENCE OF METABOLIC SYNDROME COMPONENTS AND ATHEROGENIC INDEX IN OBESE NONDIABETICCHILDREN: ANTHROPOMETRIC COMPARISON WITH PARENTS	FAWZIYA ALYAFEI	Received

94-P2	Phenotype, Genotype and Follow-up of Pediatric Hypertriglyceridemia: An Indian Perspective	Sayan Banerjee	Received

94-P3	Real-life Experience of Liraglutide Treatment and Weight Control in Obese Adolescents: A Preliminary Study Supported by Psychoanalysis	HASAN KARAKA&350;	Received

95-P3	FRUCTOSE INTAKE IS ASSOCIATED WITH MASLD IN PEDIATRIC OBESITY	Mariangela Chiarito	Received

95-P2	The Effect of Vitamin D Supplementation on Fatty Liver Disease and Insulin Resistance	Huseyin Anil Korkmaz	Received

95-P1	Phenotypes linked to duplication upstream of SOX9: New insights into presentation and diagnosis	TULAY GURAN	Received

96-P3	Correlation between the onset of hyperlipidemia and increased IGF-1 concentrations in obese children	Justyna Szydlowska-Gladysz	Received

97-P1	Long term follow up of children with intrathyroidal ectopic thymus	Carla Bizzarri	Received

97-P2	Improvement of Cardiometabolic Risk Factors and Psychosocial Health in Children and Adolescents with Excess Adiposity following Implementation of a Comprehensive, Multidisciplinary, Personalized, Lifestyle Intervention Program	Aikaterini Vourdoumpa	Received

97-P3	Prevalence and hormonal correlates of arterial hypertension in overweight/obese children.	Willem Staels	Received

98-P2	The role of Glucagon-Like Peptide 1 Receptor Agonists for Weight Control in Individuals with Acquired Hypothalamic Obesity- A Systematic Review	Nicholas Beng Hui Ng	Received

99-P1	Transient congenital hypothyroidism in a newborn with congenital goiter and compound heterozygosity for thyroglobulin	Elise Nauwynck	Received

99-P2	Body Composition in Pediatric Patients with Craniopharyngioma following Surgical Treatment	Avivit Brener	Received

100-P1	Evaluating Malignancy in Pediatric Thyroid Nodules: The Effectiveness of the Bethesda System and TIRADS	Natalia Gazek	Received

101-P1	Genetic analyses in a cohort of pediatric patients with congenital hypothyroidism based on congenital hypothyroidism consensus guideline	Erdal Kurnaz	Received

101-P3	Correlation of body mass index and insulin resistance in obese and overweight children and adolescents - a single center study	Milica Jakovljevic	Received

102-P1	DIAGNOSIS AND TREATMENT OF A CHILD AFFECTED WITH A NOVEL THYROID HORMONE RECEPTOR ALPHA (THRA) GENE MUTATION	MARIA FELICIA FAIENZA	Received

102-P2	Diagnosis of monogenic obesity: the uncertainty due to the occurrence of VUS has decreased over time. A single center experience of variant follow-up.	Anita Morandi	Received

102-P3	Early-onset obesity in a child with developmental delay and autism spectrum disorder (ASD) - a result of a new ADNP gene mutation	Sonya Galcheva	Received

103-P1	The Relationship Between Antiepileptic Drug Use and Central and Peripheral Thyroid Hormone Sensitivity	Elif Tuge Tunca Küükali	Received

103-P2	Different impact of BMI on bones mineralisation between obese and lean boys : Cross-Sectional Study	Emeriau Fabienne	Received

103-P3	Promising Horizons: The Impact of GLP-1 Agonist Therapy on Pediatric Obesity Outcomes	Arhire Amalia Ioana	Received

104-P1	Thyroid nodules in children and adolescents: 26 years of experience in a large single academic center	Athanasia STOUPA	Received

104-P3	First report of a case of Wernicke Encephalopathy due to Acute Avoidance and Restrictive Food Intake in an Adolescent with insatiable hunger due to Melanocortin 4 Receptor Deficiency: a seemingly contradictory combination	Eline van der Walle	Received

104-P2	Silent Dangers: How Insulin Resistance and Trimethylamine N-Oxide Fuel Early Atherosclerosis in Obese Children. A preliminary study	MONICA SIMINA MIHUTA	Received

105-P1	Presentation and outcome of ATA-Pediatric low-risk differentiated thyroid carcinoma (PLR-DTC) with high-invasive molecular alterations	Patricia Papendieck	Received

105-P3	A rare case of Sitosterolaemia in a paediatric patient presenting with multiple xanthomas	Eleanor Burke	Received

106-P2	Comparative Analysis of the Discriminative Ability of BMI, TMI, and BMI zscore in Establishing Metabolic Syndrome Risk	Gloria Bueno-Lozano	Received

106-P3	Syndromic and monogenic obesity: Is clinical exome sequencing necessary?	Hatice Nursoy	Received

106-P1	When Should We Consider Congenital Adrenal Hyperplasia in Children with Premature Pubarche: Key Features for Differential Diagnosis	Sebla Günes	Received

107-P3	Clinical, Laboratory, and Molecular Characteristics Of Cases With Early-Onset Obesity: a single-center experience in Egypt.	Yasmine Abdelmeguid	Received

107-P1	Non-invasive biochemical monitoring for Congenital Adrenal Hyperplasia: use of urinary steroid metabolites and salivary 17a-Hydroxyprogesterone	Joseph Tonge	Received

107-P2	Xq27.3-q28 Duplication Containing FMR1 Gene: Case Presentation and Literature Review of Familial X-linked Hypogonadism, Gynecomastia, Short Stature, Intellectual Disability and Obesity Syndrome	Mehmet Ali Oktay	Received

108-P1	Surveillance for phaeochromocytoma in children with changes in the SDHB gene may reduce morbidity: Contrasts in parent and child cases	Elham Atiq	Received

108-P3	CHALLENGES IN THE TREATMENT OF COMPLEX CASES OF HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA	Valentina Mancioppi	Received

108-P2	Prevalence and risk factors of Metabolic Associated Fatty Liver Disease (MAFLD) in polish children and adolescents with severe obesity.	Ewa Kostrzeba	Received

109-P1	Prevalence of Adrenal Insufficiency in Patients with Nephrotic Syndrome: A Prospective Observational Study	Arpita Bhriguvanshi	Received

110-P1	Does timing of Adrenocorticotropic hormone stimulation test matter?	Liat de Vries	Received

110-P2	Identification of menstrual disorders in Polish adolescent girls with severe obesity. Preliminary results of the Polish-German research project on early-onset severe obesity	&379;aneta Malczyk	Received

110-P3	Correlation between bone remodeling biomarkers and glucose metabolism in pediatric patients with essential obesity	Serena Sbilordo	Received

111-P2	The level of vascular endothelial adhesion factor (VEGF) correlate with hyperlipidemia in obese children and type 1 diabetes in important as the marker of cardiovascular disease.	Zaklina Tomczyk	Received

111-P1	Impact of ACTH on Plasma Aldosterone Concentrations in Healthy Subjects: A Systematic Review and Meta-Analysis	George Paltoglou	Received

112-P3	EVALUATING THE EFFICACY OF LIRAGLUTIDE IN THE OBESITY CHILDREN	Gunduz Ahmadov	Received

112-P2	Risk Factors for Obesity in Children with Hypothalamic Masses	Fulya METE KALAYCI	Received

113-P2	Impact of Semaglutide on body composition, cardiometabolic variables, glycaemic status, and quality of life in adolescents with severe obesity	Anand Ramakrishnan	Received

113-P3	Infantile Blounts disease: an unusual presentation of severe early-onset obesity due to LEPR mutation.	Yasmine Abdelmeguid	Received

113-P1	A NOVEL GENETIC VARIANT IN SPHINGOSINE-1-PHOSPHATE LYASE CAUSING PRIMARY ADRENAL INSUFFICIENCY AND INBORN ERROR OF IMMUNITY	Maria Elisa Amodeo	Received

114-P1	IGF1R is most highly expressed in human iPS cell-derived proliferating chondrocytes: an approach to molecular mechanisms of IGF1 action in the human growth plate	Masanobu Fujimoto	Received

114-P2	The Association between Metabolic markers, Liver function enzymes, Vitamin D level, and Lung Function Tests in Overweight/obese Children with and without Asthma	Elwaseila Hamdoun	Received

115-P3	Bariatric surgery in adolescents - one center experience	Kamila Szeliga	Received

115-P1	Unusual Presentation of Tumor-Induced Osteomalacia with Suppressed FGF-23 in an 8-Year-Old Boy	Worapimon Lerdrassameethad	Received

115-P2	Changes in Weight Distribution & Trends in Obesity Prevalence among Children and Adolescents in East Asia: Insights from NCD-RisC Data	Yong Hee Hong	Received

116-P1	Health related quality of life (HRQoL) of adolescents with XLH treated with burosumab at the end of skeletal growth (EoSG)	Clara Utley	Received

116-P2	Prevalence of Central Obesity Among Adolescent School Children in Rural Kerala, South India.	Abraham Paulose	Received

116-P3	Genetic Determinants of Egyptian children with early obesity	Omneya Magdy Omar	Received

117-P2	A paediatric case of Progeroid Lipodystrophy: diagnosis, follow-up and new insights from a de novo mutation in the POLD1 gene.	Matteo Cerutti	Received

117-P1	GH and Vosoritide combination: report of clinical experience in two girls with achondroplasia and GH deficiency	Alessandro Barbato	Received

118-P2	Semaglutide treatment for severe obesity after craniopharyngioma surgery with or without radiotherapy.	Ann-Margrethe Rnholt Christensen	Received

118-P1	Patient-Centred Data Collection Provides Comprehensive Insights into Healthcare Resource Use in Achondroplasia: Data From the Pilot Phase of the VIrtual STudy in Achondroplasia (VISTA)	Amin Ghane	Received

118-P3	A retrospective evaluation of pediatric patients admitted with hypoglycemia in terms of etiology	Esra Deniz PAPATYA AKIR	Received

119-P2	Use of medical technology and daily weight measurements in the management of severe childhood obesity	James OBrien	Received

119-P1	Craniometaphyseal Dysplasia Mimicking Infantile Osteopetrosis: A Case of Skeletal Hyperostosis and Calcipenic Rickets	Karn Wejaphikul	Received

119-P3	Experience with Octreotide-LAR in Hyperinsulinemic Hypoglycemia	Kiymet Karagoz	Received

120-P1	Health-related quality of life (HRQL) in paediatric patients with X-linked hypophosphatemia (XLH) in France: analysis of observational real-world registry data	Haruka Ishii	Received

120-P3	A challenging case of neonatal electrolyte abnormalities	Laura Corbelli	Received

121-P2	Anthropometric, Laboratory and Clinical Evaluation of Patients with Syndromic Obesity Regarding to Their Genetic Diagnoses	Gokce Velioglu Haslak	Received

121-P1	Lower Limb deformity in different types of rickets-A systematic literature	Anahita Mayr	Received

121-P3	TREATMENT OF AN INFANT WITH CONGENITAL HYPERINSULINISM DUE TO KCNJ11-MUTATION WITH OCTREOTIDE VIA CONTINUOUS SUBCUTANEOUS INFUSION: A CASE REPORT	Olimpia Alice Manzardo	Received

122-P3	Challenging management of an extreme preterm neonate with persistent hypoparathyroidism	Cristina Partenope	Received

122-P1	Good response to bisphosphonate therapy in monozygotic twins with SCN8A mutations presenting with multiple fractures associated with seizures	Thabitha Jebaseeli Hoole	Received

123-P3	GLI2 variant associated with hypopituitarism and midline defects	Gabriella Cinzia Pozzobon	Received

123-P1	Severe Diazoxide-Unresponsive Congenital Hyperinsulinism Evolving to Diabetes in Early Adolescence Caused by a Homozygous p.(Cys26Tyr) ABCC8 Variant	Maha Abdulhadi-Atwan	Received

124-P2	Genetic Causes of Obesity in children from a tertiary hospital in UAE	ANJU JACOB	Received

124-P1	Comprehensive genetic analysis of Japanese patients with congenital hyperinsulinism	Shinji Higuchi	Received

124-P3	Cause of Hypoglycemia in a Case with Turner Syndrome: Hyperinsulinemic Hypoglycemia	Aslihan Arasli Yilmaz	Received

125-P3	Impact of Sex Steroid Priming on Growth Hormone Stimulation in Children with Short Stature: A Comparative Study	FAWZIYA ALYAFEI	Received

125-P2	The Metabolic Effect of Liraglutide as Add on Treatment to Lifestyle Modification on Obese Adolescents in a Tertiary Centre, Riyadh.	Amir Babiker	Received

125-P1	RISING TREND OF TYPE 2 DIABETES FOLLOWING COVID-19 PANDEMIC IN PAEDIATRIC AGE GROUP	Abraham Paulose	Received

126-P2	First year outcomes in a Paediatric Complications of Excess Weight (CEW) Service	Khadiga Osman	Received

126-P3	Unusual presentation of Growth hormone presentation (GHD	FAWZIYA ALYAFEI	Received

126-P1	Non-invasive techniques to detect early signs and determinants of diabetic peripheral neuropathy in children with type 1 diabetes.	Miriam Eilers	Received

127-P3	A challenging case of Growth hormone deficiency (GHD) during the neonatal period	FAWZIYA ALYAFEI	Received

127-P2	MC4R VARIANT IN A FOUR-GENERATION FAMILY WITH EARLY-ONSET SEVERE OBESITY	Eleni Giannopoulou	Received

128-P1	EFFICACY AND SAFETY OF THE TANDEM T:SLIM X2 WITH CONTROL-IQ AUTOMATED INSULIN INCHILDREN WITH TYPE 1 DIABETES PREVIOUSLY TREATED WITH MULTIPLE DAILY INSULIN INJECTIONS	Raghad Alhuthil	Received

128-P3	Enhancing Diagnostic Accuracy in Growth Hormone Deficiency: A Comparative Analysis of Sex Steroid Priming in Pediatric Short Stature	FAWZIYA ALYAFEI	Received

128-P2	PLXNA1 as a Candidate Gene for Monogenic Obesity	Tara Al-Barazenji	Received

129-P3	Exploring the Impact of Growth Hormone Therapy on Glucose and Insulin Metabolism in Children with GH Deficiency: A Review	FAWZIYA ALYAFEI	Received

129-P2	Evaluation of genetic etiology and genotype-phenotype association in endogenous obesity	Esra Koyi&287;it	Received

130-P1	Evaluation of children with secondary diabetes; a single center study over a ten year-period	Emine Aya	Received

130-P2	Genetic etiology and clinical phenotype of childhood obesity based on whole exon sequencing technology	Hui Huang	Received

130-P3	OUTCOMES OF HORMONE REPLACEMENT THERAPY IN CHILDREN WITH ISOLATED IDIOPATHIC GROWTH HORMONE DEFICIENCY	Thi Ngoc Anh Tran	Received

131-P2	The Impact of Congenital Hyperinsulinism on Family Finances and Time: A Report from the HI Global Registry	Lauren Lopez	Received

131-P3	Comparison of Growth Hormone Stimulation Tests in Prepubertal Children with Short Stature According to Response of Growth Hormone Replacement	Seong Hwan Chang	Received

132-P2	A RARE METABOLIC DISEASE MIMICKING STARVATION HYPOGLYCEMIA: FRUCTOSE 1-6 BISPHOSPHATASE DEFICIENCY	Sebla Günes	Received

132-P3	Factors influencing adherence and therapy-related stress in children and adolescents on daily rhGH treatment.	Domenico Corica	Received

132-P1	The proteome of circulating exosomes in appropriate- versus small-for-gestational-age infants: differentially expressed proteins at birth associate with measures of weight gain, liver fat, insulin resistance and adrenarche at age 7	Marta Díaz	Received

133-P1	The effect of a lifestyle intervention program of diet, sleep and exercise on apelin-12, vaspin and resistin concentrations in children and adolescents with overweight and obesity	Sofia-Iliada Karampatsou	Received

134-P3	Beyond the phenotype. Report of 3 patients with non-typical Noonan Syndrome	Paula Plomer	Received

134-P1	The prevention of childhood obesity is a priority: preliminary results of the EpPOI: Education to Prevent Childhood Obesity project	Letteria Anna Morabito	Received

134-P2	LONG-TERM FOLLOW-UP OF CHILDREN AND ADOLESCENTS WITH CONGENITAL HYPERINSULINISM: A 16 YEARS SINGLE CENTER EXPERIENCE	Michaela Nikolaou	Received

135-P3	Exploring healthcare professionals perception and intent towards utilisation of digital solutions in the management of growth hormone therapies: A Taiwanese participatory study	Ekaterina Koledova	Received

136-P3	Benefits and risks of integrating digital health solutions in patients receiving growth hormone therapy in Hong Kong: Findings from an experts panel	Ekaterina Koledova	Received

136-P1	PODiaCar-Fight against Pediatric Obesity: from a predictive tool for type 2 Diabetes and Cardiovascular diseases risk to healthy educational programs	Virginia Rossi	Received

136-P2	Hypoglycemia workup in pediatric emergency room before and after an implementation of an improved management protocol	Adi Auerbach	Received

137-P1	Evaluation of VEGF, MMP-9 and visfatin levels in adolescent girls with polycystic ovary syndrome and abdominal obesity	Karolina Skrzynska	Received

137-P3	Atrioventricular Block in a Patient Small for Gestational Age during hGH Treatment	Sokratis Katsoudas	Received

137-P2	Isolated Speech and Mild Global Developmental Delay with Abnormal Genetic Microarray and IGF1 Resistance in a 6-Year-Old Female	fawziya alyafei	Received

138-P2	Comparative Growth Trajectories of SGA and AGA Preterm Infants Over the First Five Years	FAWZIYA ALYAFEI	Received

138-P1	Enhanced Metabolic Profiles Following Exercise Training in Children	Virginia Rossi	Received

138-P3	GROWTH HORMONE DEFICIENCY IN A CHILD WITH KNOWN GM1 GANGLIOSIDOSIS	Vasiliki Bekiou	Received

139-P1	The effect of pharmacotherapy compared to lifestyle intervention on body composition in children and young people managed within a multidisciplinary weight management service	Hannah Dixon	Received

139-P3	Growth Hormone Therapy in Congenital Tufting Enteropathy: A Case Report and Literature Review	Mehmet Ali Oktay	Received

139-P2	Postnatal Growth Patterns of Small for Gestational Age Infants Under 1.5 kg Over a Five-Year Period	FAWZIYA ALYAFEI	Received

140-P2	Postnatal Growth Trajectories for 5 years for AGA Preterm Infants Born 1.5 kg.	FAWZIYA ALYAFEI	Received

141-P2	Insight into IGF1 Receptor Gene Mutations: Implications for Growth Disorders and Treatment - A Comprehensive Review	FAWZIYA ALYAFEI	Received

141-P3	A RARE CAUSE OF SHORT STATURE : ELLIS-VAN CREVELD SYNDROME	Gizem Esme Kocaman	Received

142-P1	The effect of a personalized, lifestyle intervention program on SFRP5 concentrations in children and adolescents with obesity	DIAMANTO KOUTAKI	Received

142-P2	Comparative Study of Glucose Response to Intramuscular Glucagon in Pediatric Growth Hormone Deficiency and Idiopathic Short Stature: What is the risk of hypoglycemia?	FAWZIYA ALYAFEI	Received

142-P3	Growth Hormone and Scoliosis; Cause or Coincidence?	Hajer Alzahrani	Received

143-P2	Retrospective Analysis of Early Growth Patterns in Children Diagnosed with Growth Hormone Deficiency	FAWZIYA ALYAFEI	Received

143-P3	GH therapy in idiopatic short stature: an apportunity to always take into	Sabrina Criscuolo	Received

143-P1	Increased early cardiovascular risk in childhood brain tumor survivors	Soncka Jazbinsek	Received

144-P1	Age different in anti-obesity treatment targeting BAT with Ang1-7	Jun Mori	Received

144-P2	Growth Aberrations in a Yemeni Girl with Elevated IGF-1 Due to a PAPPA2 Gene Mutation: A Case Report	FAWZIYA ALYAFEI	Received

144-P3	GHD in Eastern Algeria	nadira rouabah	Received

145-P3	Severe growth deficiency in a patient with extreme short bowel syndrome and growth hormone deficiency - is there an effective treatment option ?	Dawid Goncerz	Received

145-P1	Food deserts and deprivation: Experience from a Complications of Excess Weight Service in UK	Shien Chen Lee	Received

145-P2	Comparison of growth hormone therapy response according to the presence of growth hormone deficiency in short stature children born small for gestational age in Korea.	Ha Young Jo	Received

146-P3	The Impact of Growth Hormone Therapy on Glucose Metabolism in Individuals with Turner Syndrome: A Comprehensive Review	FAWZIYA ALYAFEI	Received

146-P1	Evaluation of microvascular abnormalities and metabolic status in children with non-syndromic early-onset severe obesity using nailfold capillaroscopy	Ummahan Tercan	Received

146-P2	Clinical characteristics and treatment efficacy evaluation in Lithuanian cohort patients with severe primary IGF-1 deficiency	Ruta Navardauskaite	Received

147-P2	Is somatotropin therapy lowering the risk of SARS-CoV-2 infection in children with growth hormone deficiency and idiopathic short stature?	Gherta Bril	Received

147-P3	Accuracy of the Algerian Growth Chart in diagnosing growth hormone deficiency	ADEL DJERMANE	Received

148-P2	The Diagnostic Effectiveness of Low IGF-1 Combined with a Single Insulin Tolerance Test for the Diagnosis of Growth Hormone Deficiency	Worapimon Lerdrassameethad	Received

149-P1	Obstructive sleep apnea impairs insulin clearance and hepatic insulin sensitivity in children and adolescents with obesity	Giuseppina Rosaria Umano	Received

149-P3	A Retrospective Evaluation of Endocrinological Problems in Patients with Down Syndrome	Esra Deniz PAPATYA AKIR	Received

149-P2	Real-world experience of using Long-Acting Growth Hormone Somatrogon in children and adolescents with growth hormone deficiency	Gianluca Tamaro	Received

150-P2	Real-world data on growth hormone therapy adherence using a connected injection device and catch-up growth in children with growth disorders in Serbia	Ekaterina Koledova	Received

150-P3	Peer bullying occurs frequently among school-aged children who are short in stature.	Esra Deniz PAPATYA AKIR	Received

150-P1	Heterozygous Familial Hypobetalipoproteinemia: description of phenotype in affected children and adolescents in the Era of Obesity.	Patrizia Bruzzi	Received

151-P2	Quality of Life and Treatment Burden of Greek children and adolescents with growth hormone deficiency	Evangelia Baxevanidi	Received

151-P3	Assessment of growth in children with iron deficiency anemia treated with ferrous iron.	Simone Foti Randazzese	Received

151-P1	An old disease: New problem. Why should pediatric endocrinologists recognize Wernickes Encephalopathy due to thiamine deficiency?	Ahmet Kahveci	Received

152-P3	Unusual case of Noonan or Turner Syndrome Why not think about Escobar Syndrome?	Caroline Rosa Pelliciari	Received

152-P2	Successful Treatment of increasing chronic Hypoglycaemia by long acting GH a 15 y old girl with reduced GH Secretion	Matthias Börschel-Thomsen	Received

152-P1	Etiology of severe primary isolated growth hormone deficiency: a next-generation sequencing analysis of a single center cohort	Lukas Plachy	Received

153-P3	A case of Albright Hereditary Osteodystrophy (AHO)- Journey to diagnosis.	Ines Dakhlia	Received

153-P2	EVALUATION OF MINUTES RELATED TO THE MAXIMUM LEVELS AND RANDOM BASAL LEVELS OF GROWTH HORMONE DURING STIMULATION TEST WITH GLUCAGON	Laman Sultanova	Received

153-P1	Enhancing growth hormone treatment adherence in Argentina: A patient support programme approach	Ekaterina Koledova	Received

154-P1	Growth chart with cut-offs for poor growth response to growth hormone therapy using worldwide data in patients with growth hormone deficiency and small for gestational age	Ekaterina Koledova	Received

154-P2	Two Clinical Cases of Growth Hormone Insensitivity Overlapping Disorders: STAT3 Gain-Of-Function Syndrome and Meier-Gorlin Syndrome.	Giulia Del Medico	Received

154-P3	An unusual association of Beckwith-Wiedemann syndrome with congenital hypothyreosis, cutaneous haemangiomas and diaphragmatic eventration	Atifete Ramosaj Morina	Received

155-P2	Short and long-term response to rhGH therapy in short children born at very low birth weight.	Alexsandra Christianne Malaquias	Received

155-P1	World-wide use of the Growzen Buddy smartphone app to improve adherence in patients receiving recombinant human growth hormone therapy	Ekaterina Koledova	Received

155-P3	A Rare Cause of Short Stature in Boys: Lysineuric Protein Intolerance and Growth Hormone Experience	Gizem Bakir	Received

156-P1	Real-world adherence to growth hormone treatment and catch-up growth in children with growth disorders from the French SCOPE study	Ekaterina Koledova	Received

156-P3	Growth Hormone Therapy in a Patient with Leri-Weill Dyschondrosteosis Presenting with Madelung Deformity	Kiymet Karagoz	Received

156-P2	Dosage of recombinant human growth hormone across geographic regions at enrolment into the Kabi/Pfizer International Growth Study (KIGS)	Mitchell Geffner	Received

157-P3	Radiographic features and response to growth hormone therapy for SHOX deficiency: A case series	Aiko Sugiura	Received

157-P1	The Long-Term Follow-up of Growth Hormone Treatment in a Case with 2q37 Deletion, 14q32 Duplication and Alopecia Totalis	CANSU CEREN ERYILMAZ	Received

157-P2	Investigation of Short Stature in a 10-Year-Old Girl with STAT3 Gain-of-Function Syndrome	Lydia Mavraki	Received

158-P2	Healthcare professional (HCP) perceptions towards Mallya Connectivity Cap & App for long-acting growth hormone: results from a Slovenia Participatory Study	Primo Kotnik	Received

158-P3	A patient with of 45,X/47,XXX mosaic Turner syndrome and unusual presentation	Teodora Karamfilova	Received

158-P1	Tailoring the long-acting GH therapy in the real life	Chiara Mozzato	Received

159-P3	Results from the first stage of the Programme for early detection and follow-up of children born small for their gestational age in Bulgaria	Tanya Zlateva	Received

159-P2	Correlation Patterns in Longitudinal Growth of Preterm AGA Infants with Birth Weight 1.5 kg Over Five Years	FAWZIYA ALYAFEI	Received

160-P2	Early Growth Decline in Children with Growth Hormone Deficiency: A Comparative Study with Emphasis on Rapid Catch-Down Growth during early infancy.	FAWZIYA ALYAFEI	Received

160-P1	Systematic Approach To Define Clinically Significant Variants of Unknown Significance (VUS) in Children With Short Stature	Annalisa Deodati	Received

160-P3	Belated diagnosis of Silver-Russell Syndrome (SRS): Presentation of three cases	Ilektra Toulia	Received

161-P2	Long-Term Effects of Estrogen and Growth Hormone Replacement on Mortality and Comorbidities in Turner Syndrome	Pen-Hua Su	Received

162-P2	Leptin, ghrelin, and nesfatin-1 in children born small for gestational age with catch up growth	Hye Jin Lee	Received

162-P3	Three cases of rare bone dysplasias	Petra Tvrda	Received

163-P3	A case of PIK3CA-related overgrowth syndrome with hypertrophy of the right index finger and upper limb	Jun Mori	Received

163-P1	Real-world utility of diagnostic gene panels for severe childhood growth failure and multiple pituitary hormone deficiency in the UK	David Lim	Received

163-P2	Noonan Syndrome: About 21 cases	MALEK IABBASSEN	Received

164-P1	Prevalence of failure to thrive (FTT) in infants with Prader-Willi syndrome and the long-term effects of GH-treatment on FTT cases	Demi Trueba - Timmermans	Received

164-P3	Design and objectives of Study 111-902: a multicenter, prospective and retrospective observational study of children with hypochondroplasia	Andrew Dauber	Received

165-P3	Turner syndrome: Genotype vs Phenotype correlation.	NOOR-U-AIN MEHAK	Received

165-P2	Pattern of growth and pubertal development in a patient with MIRAGE syndrome.	Kenichi Miyako	Received

165-P1	A deep learning recognition model based on hand bone features for screening Turner syndrome	Yirou Wang	Received

166-P1	Growth hormone therapy in patient with overlap syndrome: growth outcome after one year of treatment.	Giovanni Luppino	Received

166-P2	Successful Radiofrequency Ablation of Bilateral Macronodular Adrenal Cortical Disease for Cushing Syndrome in a 6-Year-Old Girl: Preservation of Adrenal Function	Dau-Ming Niu	Received

167-P3	Efficacy of alternative Somatropine-rhGH treatment for the management of SHOX-related short stature	Chiara Mozzato	Received

167-P2	Kenny - Caffey syndrome type 2 - uncommon cause of short stature	Nguyen Thu Ha	Received

167-P1	Familial Noonan Syndrome due to mutations in PTPN11 and PLOD1 genes	Shiga Chirayath	Received

168-P1	Pubertal induction amongst girls with Turner Syndrome: oral vs patch oestrogen over the last 16 years.	Eleanor Lloyd-Jones	Received

168-P2	Pediatric Floating-Harbor Syndrome: Clinical Features and Treatment Outcomes in a Cohort of Chinese Children	Yanmei Sang	Received

168-P3	CLINICAL CASE OF A FAMILY VARIANT OF STOWN STALLING CAUSED BY A MUTATION IN THE NPR2 GENE	Zinaida Zyuzikova	Received

169-P2	Students in Turkey show a continuing positive secular change of height but a worrying increase of overweight in males	Ozge Bayrak Demirel	Received

169-P1	Compliance in children with growth hormone deficiency treated with recombinant growth hormone (rhGH): a multicentre study in Poland.	Dorian Scheuring	Received

170-P1	Growth hormone therapy is not efficient in improving the adult height of children with Hypochondroplasia	Caroline Rosa Pellicciari	Received

170-P2	Assessment of combined growth hormone and gonadotropin-releasing hormone analog treatment for patients with Silver-Russell syndrome	Amelie Perriere	Received

171-P2	Development and validation of a deep learning algorithm for predicting vitamin D deficiency risk in children using routine laboratory tests	Jo-Ching Chen	Received

171-P1	Referrals for short stature to a regional pediatric endocrinology referral: Similarities, trends, and variations in 692 children over 10 years	Fozia Memon	Received

172-P3	NOONAN SYNDROME: CASE REPORT OF 4 PATIENTS	Amel Mokrane	Received

172-P2	European Achondroplasia Forum Assessing Outcomes in a New Era of Achondroplasia Treatment	Andrea Szkuban	Received

173-P1	Incidence of delayed puberty: A nationwide register-based study.	Charlotte E. Thomsen	Received

173-P2	Prevalence and changes in genetic and clinical abnormalities in growth hormone-treated girls with Turner syndrome: a study from the Belgian-Luxembourgish growth hormone registry (BELGROW)	Laure Boutsen	Received

174-P1	International Practice in Management of Puberty for Patients with Hypogonadotropic Hypogonadism	Sebastian Castro	Received

174-P2	A Chinese case report of X-linked acrogigantism caused by Xq26.3 microduplication	Miao Qin	Received

175-P2	Endocrinopathy in patients with Prader-Willi syndrome: A single center cohort study	Bina Kim	Received

176-P3	Evaluation of an infant formula with large, milk phospholipid-coated lipid droplets on long-term growth and adiposity: Saturn study	Demi Dorrepaal	Received

176-P2	What is The Most Effective Method for Predicting Adult Height in Boys with Constitutional Delay of Growth and Puberty?	Gözde Ak&305;n Ka&287;&305;zmanl&305;	Received

176-P1	Pelvic ultrasound and pubertal attainment in girls with sexual precocity: the pivotal role of uterine volume in predicting the timing of menarche	Alessandro Cattoni	Received

177-P3	Pseudohypoparathyroidism and Turner syndrome: a case report	Meriem Benterki	Received

177-P1	Androgen Receptor Cag Repeat Polymorphism Might Be A Possible Cause of Familial Constitutional Delay in Growth and Puberty	Gözde Akın Gozde Kagızmanlı	Received

178-P3	Chromosomal abnormalities and phenotypic features in algerian paediatric population with Turner Syndrome.	Rawda Aboura	Received

178-P2	Co-Occurrence of DNET and Lymphoma in a patient with Noonan syndrome and mutation in PTPN11 gene	Caroline Rosa Pellicciari	Received

178-P1	Investigation of the Emotional and Psychosocial Dimensions of Girls Diagnosed with Idiopathic Central Precocious Puberty	Arzu Jalilova	Received

179-P3	Brazilian children with severe short stature and Batter syndrome type 3: a case series	Andrea de Castro Leal Novaes	Received

179-P2	An Uncommon Cause of Short Stature: 18q Deletion	Elif Tuge Tunca Küükali	Received

179-P1	A 31-year referral center experience in pediatric growth hormone secreting pituitary adenomas.	Maria Hernandez	Received

180-P1	Retrospective Analysis of Pediatric Craniopharyngioma at a National Referral Center: A 37-Year Experience. Clinical Characteristics and Treatment Outcomes.	Maria Hernandez	Received

180-P2	A Rare Case of Short Stature and Hypergonadotropic Hypogonadism: LIG4 Mutation	Agh Akin	Received

180-P3	Sleep disturbances among 4 to 12 year-old Filipino children with drug resistant epilepsy in a Pediatric Tertiary Hospital in the Philippines	Cherise Andrea Llaneta	Received

181-P1	Characterization of puberty-regulating microRNAs within the hypothalamus of female mice	Pavlos Fanis	Received

181-P3	Impact of Nutrition and Endocrinal Complications on Growth Pattern of Children with Sickle cell Disease	Radwa Shamma	Received

181-P2	Mimicking the diagnosis - new challenge for pediatric endocrinology?	Eva Vitariusova	Received

182-P3	THE OUTCOME OF ONGOING ADULT ENDOCRINE ENGAGEMENT FOLLOWING TRANSITION FROM PAEDIATRIC CARE	Xin Yean Chai	Received

182-P1	A description of a national meeting for hypothalamo-pituitary-axis-tumours	Bryan Padraig Finn	Received

183-P2	Growth disorders and endocrine problems in children with FASD	Agnieszka Domin	Received

183-P1	Arginine-stimulated copeptin for Central Diabetes Insipidus diagnosis in children.	Flavia Napoli	Received

184-P1	Assessment of hypogonadotropic hypogonadism using a gonadotropic-gonadal stimulation test with subcutaneous Triptorelin: preliminary results.	Analía Freire	Received

184-P2	Impact of Growth Hormone Therapy in Small for Gestational Age (SGA)	Arzu Jalilova	Received

185-P2	A clinical follow-up of 46 Algerian patients with Prader Willi-Syndrome and their endocrine profile	sakina kherra	Received

185-P1	Genetic analysis of a European cohort of ROHHAD patients	Federica Buonocore	Received

185-P3	From endocrine phenotype to hematological diagnosis of Fanconi anemia apropos of 2 cases	Corina Ramona Nicolescu	Received

186-P2	Aggrecan mutation in amidst of congenital neuropathy: what is the relevance of an early genetic diagnosis?	Francisco Branco Caetano	Received

186-P1	Utility of First-Morning-Voided Urinary Total LH in Detecting the Onset of Central Puberty	And Demir	Received

186-P3	Early Recognition and Management of Nephrogenic Diabetes Insipidus in preterm newborn: A Vital Case Study	Sommayya Aftab	Received

187-P1	Moderate day-to-day variation in first morning urine total luteinizing hormone levels supports the use of a single determination to identify imminent puberty	And Demir	Received

187-P3	Hypophosphaemic rickets, central precocious puberty and epidermic neavus syndrome	nadira rouabah	Received

187-P2	Chronic autoimmune thyroiditis and Say- Barber -Biesecker- Young- Simpson syndrome: description of a case of unusual association	Tiziana Abbate	Received

188-P2	A patient with Rahman syndrome presenting with a novel pathogenic mutation and diabetes	Yuliya Bazdarska	Received

188-P1	Childhood-onset craniopharyngioma: 26 years of experience at Childrens Memorial Health Institute (CMHI)	Agnieszka Bogusz-Wójcik	Received

188-P3	Hypothyroidism with thyroid gland in place as the initial sign of a rare disease with typical phenotypic characteristics	Sara Soldovieri	Received

189-P2	A child with cutaneous-skeletal hypophosphatemia syndrome caused by a mosaic HRAS mutation outcome of treatment with anti-FGF23 antibody	Jing Wu	Received

189-P3	ENDOCRINOLOGICAL SEQUELAE OF PROTEIN-LOSING ENTEROPATHY IN AN ITALIAN CHILD	paolo cavarzere	Received

190-P2	Rare Cases of Primary Hypoparathyroidism in Childhood in the Covid-19 Era	George Paltoglou	Received

190-P1	The first description of an MC4R variant in a patient with Kallmann syndrome and obesity	Aisha Aslam	Received

191-P3	Exaggerated mini puberty vs central precocious puberty in an extreme preterm female, To treat or not to treat?	Abdulsalam Abu-Libdeh	Received

191-P1	Assessing quality of care for people with differences of sex development (DSD) results of an annual benchmarking of DSD centres in Germany	Ulla Doehnert	Received

192-P2	Assessment of the rhGH treatment compliance in children based on data from centres in Poland and Italy.	Dorian Scheuring	Received

192-P1	Sex Steroid Metabolite Profile and Gonadotropins during Hormone Therapy in Transgender Adolescents	Pernille Norup	Received

192-P3	EFFECT OF GNRH TREATMENT OF GIRLS WITH EARLY/PRECOCIOUS PUBERTY ON MENARCHE, MENSTRUALCYCLE STATUS, AND ONSET OF MENOPAUSE.	nada alaaraj	Received

193-P2	Impact of Growth hormone therapy in a Child with SOX3 mutation: A Case Study	Julia Karpel	Received

193-P3	Height Gain after GnRH agonist Treatment for Precocious Puberty or Early Puberty	Ja Hyang Cho	Received

193-P1	Under the Lens: A Study of Childhood Gender Identity Through the Toy Preference Test and its relation to minipuberty	Laura Lucaccioni	Received

194-P1	Consequences for treatment following the German Act on the Protection of Children with Differences in Sexual Development (DSD)	Uta Neumann	Received

194-P2	Effectiveness of therapy with recombinant human growth hormone (rhGH) in patients with HLHS and short stature	Aleksandra Furtak	Received

194-P3	Atypical Presentation of Endocrinal Disorder	Radwa Shamma	Received

195-P3	Pituitary Hyperplasia Due to Primary Hypothyroidism Apropos of 2 Cases	Corina Ramona Nicolescu	Received

195-P1	Clitoromegaly - Size does matter	Malka Ariella Brown Segal	Received

195-P2	Severe intrauterine growth retardation and diagnosis of growth hormone deficiency as initial presentation of TEMPLE syndrome	Kalina Mihova	Received

196-P1	Survey of pediatricians on the care provided to children with gender diversity	Maria Alija	Received

196-P3	Giant prolactinoma presenting as unilateral exophthalmia a case report	Corina Ramona Nicolescu	Received

196-P2	Early life growth patterns in cystic fibrosis in Infants from western Algeria	Meriem Oussalah	Received

197-P1	46 XY Gonadal Dysgenesis- Transmission of a Novel DMRT1 Mutation	Elaine C Kennedy	Received

197-P3	Isolated Premature Menarche: Management and Outcomes A case series from a UK University Teaching Hospital	Diamantina Spilioti	Received

197-P2	Adult height of children born small for gestational age treated with growth hormone in southern Brazil	Adriane Cardoso-Demartini	Received

198-P1	Course and Predictors of Puberty in Boys with Isolated Micropenis	Dhvani Raithatha	Received

198-P3	A BABY GROWN UP WITH CENTRAL HYPOTHYROIDISM	Ho Chung YAU	Received

198-P2	A Correlation Study Between Iron Overload, Chelation Therapy (ICT), and Metabolic Outcomes in -Thalassemia Major (-TDT) Patients	Ashraf Soliman	Received

199-P2	Impact of Iron Chelation Therapy Adherence on Prediabetes Development in Young Adult -Thalassemia Major Patients: A Comparative Analysis	Ashraf Soliman	Received

199-P3	Giant Rathkes Cleft Cyst Causing Panhypopituitarism	Cansu Sadiye Karadeniz	Received

200-P3	Gynecomastia in a Patient with Neurofibromatosis Type 1	Betül Liv anga	Received

200-P1	Severe congenital hypothyroidism due to a novel homozygous variant affecting the conserved CAGYC region of TSH	Nina Makretskaya	Received

201-P3	A case of Precocious Puberty in a girl with Prader-Willi Syndrome	Renato Vaiasuso	Received

201-P2	Assessment of genotype-phenotype correlation in children with pseudohypoparathyroidism	Dorota Roztoczynska	Received

202-P3	Pituitary hyperplasia secondary to primary hypothyroidism (PHPH) in a paediatric patient with fetal alcohol syndrome A case report	Eugenio Trinati	Received

202-P2	Endocrine Abnormalities and Growth Pattern in Single Large-Scale Mitochondrial DNA Deletion Syndromes	Ayman Daka	Received

203-P3	Pituitary hyperplasia secondary to primary hypothyroidism	Mabrouka M A Al Towati	Received

203-P1	Experience with Combined T4 and T3 Therapy in Childhood Hypothyroidism	ba&351;ak alan tehi	Received

204-P1	Impact of the Presence of a Feeding Tube on Tiratricol Maintenance Dosing and Efficacy Outcomes in Patients with MCT8 Deficiency	Samia Haque	Received

204-P3	Severe hypoglycemia in a 5-year-old boy with hyperprolinemia and growth hormone deficiency	Ilektra Toulia	Received

205-P2	Congenital disorders of glycosylation (CDG): Endocrinological features in a case of twin siblings with a ALG1 gene defect.	Gisela Viterbo	Received

205-P1	Treatment Outcomes in Pediatric Differentiated Thyroid Carcinoma: A Single Center Experience	Ilayda Altun	Received

206-P2	A Case of Pediatric PTEN Hamartoma Tumor Syndrome Presenting with a Breast Mass	Hasan Bora Ulukapi	Received

207-P3	PROLACTINOMA	Muhammad Faizi	Received

207-P2	Endocrinological disturbances in patients with ROHHAD syndrome- single center data	Magdalena Ossowska	Received

207-P1	Newborn screening for congenital hypothyroidism and re-screening at two weeks of life in infants born to mothers with thyroid diseases.	Maria Cristina Vigone	Received

208-P1	The prevalence of nephrocalcinosis among patients with congenital adrenal hyperplasia due to 21 hydroxylase deficiency one-centre experience. Do we need a regular screening?	Magdalena Banaszak-Ziemska	Received

208-P3	Can InhibinB and AMH measurements help in the differential diagnosis of HHI?	Esther Angrisani	Received

208-P2	A Case of Kearns-Sayer Syndrome Presenting with Hypoglycaemia and Adrenal Insufficiency	Sandipan Paul	Received

209-P1	Early Childhood-Onset Non-Classical CAH (NCCAH) Presenting with Premature Pubarche and Clitoromegaly Caused by CYP21A2 Duplication Without Gene Mutation in Triplets	Johanna Schnitzlein	Received

209-P3	Delayed, disharmonic pubertal development as the leading symptom of IGSF1-deficiency	Stefan Riedl	Received

210-P3	Hypergonadotropic hypogonadism in a girl after bone marrow transplantation from a male unrelated donor.	Elena Shukarova-Angelovska	Received

210-P2	Endocrine Phenotypic Variability in Schaaf-Yang Syndrome: Insights from a Case Series	shira goldman	Received

210-P1	Triple A syndrome: A common cause of primary adrenal insufficiency in Algeria	Kahina Mohammedi	Received

211-P2	IMPACT OF GNRH ANALOG THERAPY ON EARLY AND FAST PUBERTY GIRLS: CLINICAL, RADIOLOGICAL AND HORMONAL ANALYSIS	fawziya alyafei	Received

211-P1	Non tumoral ACTH-Independent Cushing Syndrome in Pediatric Patients: A Retrospective Observational Cohort Study	dulanjalee kariyawasam	Received

211-P3	Fahrs Syndrome as a Manifestation of Autoimmune Polyendocrinopathy Syndrome	Bushra Rehman	Received

212-P3	A case of multiple pituitary hormone deficiency with complex brain malformations: anunusual occurence of pituitary stalk interruption syndrome (PSIS)	Tiziana DAlvano	Received

212-P1	Negative Impact of Supraphysiological Glucocorticoid Dosing on Growth and Changes in Glucocorticoid Dose and Androstenedione Health States in Patients with Classic Congenital Adrenal Hyperplasia: Results from the CAHtalog Patient Registry	Jackie Dessibourg	Received

213-P3	Koolen de Vries: a new associated malformation and an additional complex disease?	Caetano Francisco	Received

213-P1	Prematurity and low birth weight may be key indicators for a low peak cortisol on neonatal Short Synacthen Tests	Aneeq Ahmed	Received

214-P3	Time to Diagnosis and Risk Factors for Central Diabetes Insipidus Complicating Hypoxic-Ischemic Encephalopathy after Return of Spontaneous Circulation	Takehiro Honma	Received

214-P1	The unique urinary steroid metabolome in infants with P450 oxidoreductase deficiency in the first week of life	Elizabeth S. Baranowski	Received

215-P1	Who should be screened for electrolyte imbalances in the outpatient endocrinology clinic?	Raluca Pop	Received

215-P3	EMPTY SELLA SYNDROME: A CASE REPORT	Sokratis Katsoudas	Received

215-P2	Transition-loop, an educational tool that helps to provide a smooth transition to adult care for the youngster with chronic conditions. Before transition from adolescent care to adult care - necessary considerations	Camilla Ernstsson	Received

216-P3	A Case of Adipsic Diabetes Insipidus with Craniopharyngioma	Meltem Korkmaz Vural	Received

216-P2	The comparison of the timing of menarche in girls with central precocious puberty following the discontinuation of monthly and 3-monthly Leuprolide acetate.	Ekkachai Nakaviroj	Received

216-P1	Characterization of a large cohort of 99 argentinian patients with hereditary hypophosphatemic rickets (HHR) followed in a single pediatric tertiary center	Gisela Viterbo	Received

217-P1	Preterm born young men have lower lumbar spine Z-scores than preterm born young women	Ella Bruun	Received

217-P2	Multihormonal Pituitary Insufficiency as a Late Manifestation of Traumatic Pituitary Stalk Interruption.	Tomasz Jackowski	Received

217-P3	Differential Diagnosis of Pituitary Stalk Thickening in Central Diabetes Insipidus	Gizem Bakir	Received

218-P1	Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor Mutation: Experience with Cinacalcet and Parathyroidectomy	Hasan Bora Ulukapi	Received

218-P3	Hypogonadotropic Hypogonadism due to mutation of KISS1R gene in a 12 years old boy with different approach for treatment	Omair Alghamdi	Received

218-P2	Report of a patient with TUBB3 E410K syndrome: when Moebius syndrome does not quite fit	Anis Fozi	Received

219-P3	An unusual cause of precocious puberty in a young boy	Louise Apperley	Received

219-P1	Prospective longitudinal assessment of bone mineral density, circulating markers of bone turnover and changes in body composition in children and adolescents treated for acute lymphoblastic leukemia	Silvia Molinari	Received

220-P3	Septo-optic dysplasia and panhypopituitarism: a case report	Gabriella Cinzia Pozzobon	Received

220-P1	Safety and efficacy of continuous subcutaneous PTH (1-34) infusion therapy (CSPI) for severe autosomal dominant hypocalcaemia type 1 (ADH1) in Children and Young People (CYP)	Aikaterini Perogiannaki	Received

220-P2	Association between Attention Deficit Hyperactivity Disorder, Precocious Puberty and Obesity in Korean girls	Eun Byoul Lee	Received

221-P1	A 10-year non-interventional registry of patients with FGF23-related hypophosphatemic rickets and osteomalacia in Gulf Cooperation Council (GCC)	Mohammed Al Dubayee	Received

221-P3	Etiology of precocious puberty, 8 years study in a Pediatric endocrine Center in Annaba, Algeria	Nihad SELIM	Received

221-P2	CENTRAL PRECOCIOUS PUBERTY: FROM ETIOLOGIES TO OUTCOMES IN PATIENTS AT THE VIETNAM NATIONAL CHILDRENS HOSPITAL	Hang Nguyen	Received

222-P1	Expanding the clinical phenotype of PKDCC Rhizomelic Skeletal Dysplasia A Case Report and literature review	Eleanor Burke	Received

222-P3	Pituitary macroadenoma in a 17-year-old girl - therapeutic difficulties	Hanna Borysewicz-Sa&324;czyk	Received

222-P2	Genetic and clinical heterogenicity in Russian adolescents with congenital isolated hypogonadotropic hypogonadism	Kristina Kokoreva	Received

223-P2	Surgical Treatment and Somatostatin Experience in Growth Hormone-Secreting Pituitary Macroadenoma Due to AIP Mutation	Kiymet Karagoz	Received

223-P1	Determinants of bone mineral density in healthy term-born children at age 6 months	Demi Dorrepaal	Received

223-P3	Use of Desmopressin Instead of CRH for Inferior Petrosal Sinus Sampling in Children with Clinical Suspicion of Cushings Disease	Elif Kelestemur	Received

224-P3	Delayed diagnosis of congenital hypopituitarism presenting as syndromic obesity	Gabriella Pozzobon	Received

224-P1	Rare diseases, rarely diagnosed: Mapping the accuracy of laboratory screening for rare bone disorders in Austria	Adalbert Raimann	Received

224-P2	Successful Experience with Tolvaptan in Syndrome of Inappropriate Secretion of Antidiuretic Hormone	Agh Akin	Received

225-P3	Management challenges in a pediatric somatotropinoma	Gabriella Pozzobon	Received

225-P1	Lower Limb deformity in different types of rickets -A systematic literature review	Anahita Mayr	Received

225-P2	DESCRIPTION OF A COHORT OF PAEDIATRIC PATIENTS WITH CONGENITAL HIPOPYTUITARISM	Cristina Aguilar Riera	Received

226-P3	Evaluation of service provision for patients with Precocious Puberty in a District General Hospital	Cristina Matei	Received

226-P1	MICROVASCULAR COMPLICATIONS OF T1DM IN CHILDREN AND ADOLESCENTS AT TERTIARY CARE HOSPITAL, PAKISTAN.	Dr Syed Saddam Hussain	Received

227-P2	Real Life Efficacy and Safety of Monthly (4-week) and 6-Monthly (24-week) Formulations of Gonadotropin-Releasing Hormone Agonist (GnRHa) Among Children with Central Precocious and Early Fast Puberty	Libby Shopen	Received

227-P1	Higher levels of c-peptide at the onset of Type 1 Diabetes are correlated with better glycemic control after 2 years from the diagnosis in a cohort of pediatric patients.	Valentina Mancioppi	Received

227-P3	A de novo novel heterozygous deletion mutation in steroidogenic factor 1 gene (NR5A1) in a 46,XY female with sex reversal, primary adrenal insufficiency and splenic aplasia: A 13 years follow-up	Danyi Wang	Received

228-P3	The clinical conundrum of mixed gonadal dysgenesis: A case report	Thabitha Hoole	Received

228-P1	The use of pumps with Automated Insulin Delivery (HCL/AHCL) improves the Sleep Quality of Children and Adolescents with Type 1 Diabetes and of their parents/caregivers.	Valentina Mancioppi	Received

228-P2	Can Hypophysitis Mask Pituitary Stalk Germinoma? Insights from a Case Series Analysis.	Maria Hernandez	Received

230-P1	Screening for Dysglycaemia in Children Amidst a Global Obesity Crisis	Jack Sims	Received

230-P3	Does Primary Ovarian Failure associate with Monogenic Diabetes Mellitus	Muna Sharaf	Received

230-P2	Advancing Endocrine Disorder Diagnosis in Cyprus: The Cyprus Institute of Neurology and Genetics as an ENDO-ERN Reference Center	Vassos Neocleous	Received

231-P1	Children and Young People and Parent and Carer Perspectives on Provision of Type 2 Diabetes Mellitus Care in England and Wales Insights from the PREM survey report (2021/22)	Katherine Hawton	Received

231-P3	A case of isolated transient clitoral hypertrophy in extremely preterm infant with popliteal pterygium	Lavinia La Grasta Sabolic	Received

232-P1	Dietary interventions for the management of type 2 diabetes mellitus in childhood and adolescence: a systematic review	Katherine Hawton	Received

232-P3	When phenotype and genotype do not match: Risks to be analyzed.	Maria J. Chueca	Received

233-P2	Novel GLI2 Mutation in a Girl with mild holoprosencephaly presenting with Pituitary Stalk Interruption Syndrome, Central diabetes insipidus and combined pituitary hormone.	Francesca Aiello	Received

233-P3	Spontaneous Puberty in a Boy with Desert Hedgehog (DHH) Mutations with Hypospadia and Cryptorchidism after Stimulation with GNRHa and HCG/FSH during Infancy	Gunter Simic-Schleicher	Received

233-P1	Early Markers of Diabetic Nephropathy in Children and Adolescents with Type 1 Diabetes	Shereen Abdelghaffar	Received

234-P3	Clinical case of rare association of Treacher Collins syndrome with micropenis and unilateral cryptorchidism in Russian patient	Kristina Kokoreva	Received

234-P1	Diploid/triploid mosaicism: a rare cause of metabolic syndrome and diabetes in children	Anita pehar Uroi&263;	Received

234-P2	Cranberry as a Cause of Premature Menarche	ba&351;ak alan tehi	Received

235-P1	Towards a Genetic Obesity Risk Score: preliminary data from a single-centre cohort of obese children and adolescents	Cristina Partenope	Received

235-P2	A RARE CASE OF HYPOGONADOTROPIC HYPOGONADISM ASSOCIATED WITH SKELETAL ANOMALITIES: ULNAR-MAMMARY SYNDROME	Valentina Mancioppi	Received

236-P2	Achieving normal near final height in girls with idiopathic central precocious puberty and early puberty following gonadotropin-releasing hormone analog treatment: Predictors	Dolrutai Puttawong	Received

236-P1	Prevalence of variants in the Leptin Melanocortin 4 receptor (MC4R) pathway in an Israeli cohort of children with severe obesity and their clinical and laboratory characteristics	Michal Ben Ami	Received

237-P1	Health transition of children with obesity - a comprehensive approach from a German obesity center: a prospective cohort analysis	Robert Stein	Received

238-P3	New mutation in the ANOS gene associated with hypogonadotropic hypogonadism, anosmia, synkinesis and renal agenesis.	Elena Pisareva	Received

238-P1	Predictive Value of Impulse Oscillometry and Hepatic Fat Content for Obstructive Sleep Apnea Syndrome in Obese Children and Adolescents	Sercan Öztürk	Received

238-P2	Vaginal Bleeding in a Severely Premature Infant During the Mini-Puberty Period	Meltem Korkmaz Vural	Received

239-P2	Clinical Follow-Up of a Case Diagnosed with POMC Deficiency Presenting with Hypoglycemia and Cholestasis	Behiye Sarikaya Özdemir	Received

239-P1	Evolution of the cytokine profile following duodenal-jejunal bypass liner in adolescents with obesity	Igor Tercon	Received

240-P1	Patient and parent experience of a group exercise programme collaboration with a tertiary paediatric weight management service	Claire Semple	Received

240-P3	Delayed puberty: etiological and gender characteristics	Goar Okminyan	Received

241-P2	Sellar Mass Confused with Craniopharyngioma: Mature Cystic Teratoma	Aslihan Arasli Yilmaz	Received

241-P1	Genetics of obesity: results from a tertiary paediatric weight management service	Hannah Hickingbotham	Received

241-P3	The curious case of a boy with cryptorchidism	Marilea Lezzi	Received

242-P2	Single Centre Experience in the Management of Childhood Prolactinoma	Gizem Boke Kocer	Received

242-P1	GNAS mutation: an under-rated cause of severe early-onset obesity !	Yasmine Abdelmeguid	Received

242-P3	Efficacy of Letrozole in Managing Prepubertal Gynecomastia Associated with Peutz-Jeghers Syndrome: A Case Study	Hasan Bora Ulukapi	Received

243-P1	Experience with Cinacalcet in Neonatal Severe Hyperparathyroidism Due to CASR Mutation	Kiymet Karagoz	Received

243-P2	Overweight and obesity in children and young people with CNS tumours	Anand Ramakrishnan	Received

243-P3	Aphallia: a case report	akli Taazibt	Received

244-P3	A rare cause of Secondary Amenorrhoea: Sertoli-Leydig cell tumour of ovary associated with DICER-1	Buddhi Gunasekara	Received

244-P1	TEAR PROTEOMICS IN CHILDREN AND ADOLESCENTS WITH CONGENITAL HYPERINSULINISM	Michaela Nikolaou	Received

244-P2	Rapidly progressing peripheral precocious puberty due to pineal germ cell tumor in a preschool age boy	Sofia LEKKA-EMIRI	Received

245-P1	The LIFE-MILCH study: first data on the exposure to Endocrine Disrupting Chemicals (EDCs) in urine and breast milk (BM) from end of pregnancy to 12 months of life.	Francesca Alberghi	Received

245-P2	Effectiveness of the uterine artery pulsatility index as a non-invasive diagnostic method for precocious puberty and its correlation with pelvic and breast ultrasound findings, bone age, and hormonal profile	Aidy González Núñez	Received

246-P1	Rarity of congenital adrenal hyperplasia in children born verypreterm: Possible mechanism and implication for newborn screening	Asmahane Ladjouze	Received

246-P2	The role of insulin-like growth factor-I in predicting growth velocity during GnRH-agonists treatment for central precocious puberty.	Valeria Citterio	Received

247-P3	The Complex Relationship Between Thyroxine Therapy and Growth Outcomes in Pediatric Hypothyroidism	nada alaaraj	Received

248-P3	The Natural Course of Subclinical Hypothyroidism in Children and Adolescents: A Comprehensive Review	nada alaaraj	Received

248-P1	Assessment of carbohydrate and lipid metabolism in patient with glycogen storage disease type 0a and celiac disease at diagnosis and after 3 years of follow-up - case report.	Maja Okonska	Received

249-P2	PUBERTAL VIRILIZATION IN INDIVIDUALS WITH PARTIAL GONADAL DYSGENESIS ATTRIBUTABLE TO DHH MUTATION: A CASE REPORT	Aylin Günay	Received

249-P1	THE PREVALENCE OF THYROID DISORDERS AND COELIAC DISEASE IN CHILDREN WIH TYPE 1 DIABETES MELLITUS SEEN IN A TERTIARY HOSPITAL IN RESOURCE LIMITED SETTING	Tebo Thekiso	Received

249-P3	Treating versus Not Treating Subclinical Hypothyroidism (SCH) in Children: A Comprehensive Review	nada alaaraj	Received

250-P3	Thyroxines Role in Growth and Development: A Review of Clinical Effects	fawziya alyafei	Received

250-P1	In an era of advanced genomic testing- is karyotype still relevant?	Noa Shefer-Averbuch	Received

251-P1	The Use Of EQ5D For Assessment Of Health Related Quality Of Life And Its Determinants In Children With Complex Endocrine Conditions	Xanthippi Tseretopoulou	Received

251-P2	Teen pregnancy in a girl with 45,X/47,XXX-Turner syndrome in the virtual absence of serum AMH and no oocytes in ovarian histology	Gerhard Binder	Received

251-P3	Comprehensive Review on the Mechanisms of Thyroxine Action on Growth and Brain Development	fawziya alyafei	Received

252-P3	Impact of Subclinical Hypothyroidism on Pediatric Health: A Summary of Findings	nada alaaraj	Received

252-P2	Challenges in prenatal and postnatal management of 45,X/46,X, idic (Y) mosaicism	Julie Fudvoye	Received

252-P1	Growth Hormone Therapy in Prader Willi Syndrome Audit of Age of Initiation Over Time in a Tertiary Centre	edna roche	Received

253-P1	Establishing a Nurse-led Transition Clinic for Young People with Congenital Adrenal Hyperplasia (CAH): Quality Improvement Project	Angela Thompson	Received

253-P2	A Rarely Detected Variant in 46,XX Disorders of Sex Development: Recurrent p.Arg92Trp Variant in NR5A1	Mehmet Ali Oktay	Received

253-P3	Growth hormone deficiency in patients with late detected Hashimoto thyroiditis-how long to wait for treatment	Elena Sukarova-Angelovska	Received

254-P3	Chief complaints at initial presentation of children with Graves disease	Ayse Nurcan Cebeci	Received

254-P1	Growth Response to Medical Intervention in an Observational Real-life Study of Children with Growth Delay: A Causal Inference Method	Kanetee BUSIAH	Received

254-P2	Implication for metabolic heath of using of adolescent PCOS criteria	&379;aneta Malczyk	Received

255-P2	Exploring the Clinical Implications of a LARS2 Gene Mutation in a Female Adolescent with Perrault Syndrome	Júlia Galhardo	Received

255-P3	Encephalopathy in Hashimotos Thyroiditis: A Case Report	Ruta Navardauskaite	Received

255-P1	Health and life risks in children with achondroplasia multicenter study.	Wiktoria Wrobel	Received

256-P3	Van Wyk Grumbach syndrome an exciting disease with different causes and forms of presentation	Susen Reichardt	Received

256-P2	Normosmic Congenital Hypogonadotropic Hypogonadism caused a missense mutation in the GnRHR gene in a Female Adolescent	Júlia Galhardo	Received

256-P1	Height outcomes in children born small for gestational age (SGA) from combined CrescNet and REPAR cohorts: The impact of either spontaneous or growth hormone-induced catch-up growth	Aneta Kodytková	Received

257-P3	Case of Hyperthyroidism Due to Amiodarone Use for Supraventricular Tachycardia	Emine Seyma EKEN	Received

257-P2	Clinical and Laboratory Characteristics of Children with Congenital Adrenal Hyperplasia (CAH): A Comparative Study of Hypertensive and Normotensive Patients	Shaymaa Elsayed	Received

257-P1	molecular and phenotypic characteristics of chinese neurofibromatosis type 1 children	zhiying li	Received

258-P2	Impact of Precocious Puberty on Clinical Management in Pediatric Patients with Congenital Adrenal Hyperplasia	Shaymaa Elsayed	Received

258-P3	Challenges in Managing Pediatric Hypothyroidism: A Case of Severe Autoimmune Thyroiditis	Bogdan Mihai	Received

258-P1	First Real-Life Data on the Use of Long-Acting Growth Hormone Somatrogon in Türkiye	CENG&304;Z KARA	Received

259-P3	Brain-Lung-Thyroid Syndrome: differences in clinical spectrum in two case reviews	Kamal Weerasinghe	Received

259-P1	Polysomnography Findings and Respiratory Problems in Prader-Willi Syndrome: The Effect of Growth Hormone Treatment	Elif Kelestemur	Received

259-P2	Fostering Resilience: Exploring Family Support Groups for Girls with Turner Syndrome - A Pilot Study	Moran Shemesh-Iron	Received

260-P2	CARE OF TRANSGENDER CHILDREN AND ADOLESCENTS IN OUR REGION: NINE YEARS OF EXPERIENCE OF A MULTIDISCIPLINARY WORKING GROUP	Laura Bertholt	Received

260-P1	Long-Acting Growth Hormone Therapy in Children with Growth Hormone deficiency A two centre real world experience from UK	Pon Ramya Gokul	Received

260-P3	Evolution of subclinical hypothyroidism in infancy: a single-center longitudinal retrospective cohort study	Francesca Franchina	Received

261-P1	Recombinant Growth Hormone Therapy in Pediatric Renal Failure: 30-Year-Experience in a Tertiary Hospital	Silvia Gil	Received

261-P2	Attitude of the pediatric endocrinologists in the accompaniment of children with gender diversity: results of a survey	Isolina RIAÑO-GALAN	Received

262-P2	The correlation between quality of life and anthropometric indicators in boys with delayed puberty	Goar Okminyan	Received

262-P3	Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation and Autonomic Dysregulation (ROHHAD)	Nur Rochmah	Received

262-P1	A novel comprehensive bioinformatic strategy could significantly enhance the molecular genetic diagnosis in growth restriction phenotypes	Miho Ishida	Received

263-P3	Urinary iodine concentrations in schoolchildren in Serbia: still too little or too much	Ljiljana Saranac	Received

263-P1	Reduced final height in boys after allogeneic hematopoietic stem cell transplantation (HSCT) for childhood cancer: does pubertal growth spurt matters?	Vittorio Ferrari	Received

264-P1	Single center prospective study on the Efficacy and Safety of Vosoritide Therapy in Achondroplasia: A Comprehensive Evaluation at Three and Six Months	Roberta Leonardi	Received

264-P3	Ophthalmic Involvement in Childhood Graves Disease: A Report of Two Cases	&304;lkay Bahar Balaban Berber	Received

265-P1	Use of Vosoritide in Children with Achondroplasia -Real Life Experince	Ahmet Kahveci	Received

265-P2	Gonadal function and its evolution in 46, XX testicular/ovotesticular DSD	Margherita Sepich	Received

266-P3	TRAb, a nasty joke: two cases of neonatal hyperthyroidism in newborns of mothers affected by autoimmune hypothyroidism.	Maria Cristina Vigone	Received

266-P1	AFMS (Achondroplasia Foramen Magnum Score) in a case series; correlation with clinical manifestations, and sleep studies.	Kyriaki Hatziagapiou	Received

266-P2	Outcome of antenatal treatment in congenital adrenal hyperplasia due to 21 hydroxylase-deficiency in Algeria	Yasmina Ouarezki	Received

267-P2	Gynecomastia: Could It be The One and Only Symptom of The Androgen Insensitivity Syndrome?	Meltem Buhur Pirimo;lu	Received

267-P1	The clinical burden and healthcare resource utilization among children and adolescents with achondroplasia: an observational cohort study using Optums de-identified Clinformatics Data Mart Database	Yasmin Lau	Received

267-P3	Unraveling Refetoff Syndrome: Insights from a Pediatric Endocrinology Case	Maria Cristina Vigone	Received

268-P3	An unusual genetic variant in SLC16A2 causing MCT8 deficiency	Amith Ramcharan	Received

268-P1	Mechanisms of Growth Failure in a Mouse Model of Aggrecan Deficiency: Insights into Chondrocyte Function and Akt Signaling	Ameya Bendre	Received

269-P3	The comorbidity of other autoimmune diseases in children with autoimmune thyroid diseases	Justyna Michalak	Received

269-P1	Effect of treatment with Isotretinoin on early bone maturation: A Case Report	Adriane Cardoso-Demartini	Received

269-P2	Exercise and Eating Behaviors among Transgender and Gender Diverse Adolescents	Sarah Knaus	Received

270-P2	A Rare Cause of Primary Ovarian Insufficiency: Novel Homozygous c.2120GC(p.Arg707Pro) Pathogenic Variant in the MCM8 Gene	Simge Eren	Received

270-P3	Atrophic thyroiditis in a 14-year-old girl who was undiagnosed for 4 years despite growth failure	Hitomi Saiki	Received

271-P3	Challenges in Treating Simple Virilizing CAH: A Case of Accelerated Bone Maturation	Bogdan Pascu	Received

271-P1	The Use Of GloBE-Reg As A Global Platform For Performing Safety & Efficacy Studies Of rhGH Therapy	Malika Alimussina	Received

271-P2	Thyroid Function Changes During Growth Hormone Therapy in Pediatric Patients: A Review and Comparison with Recent Data	fawziya alyafei	Received

272-P2	Thyroid function during GH therapy in children with GHD versus those with ISS	fawziya alyafei	Received

272-P1	Nonfunctioning pituitary adenomas in childhood: A single-center experience	Selen Hürmüzlü Közler	Received

273-P1	Prospective assessment of hypothalamic dysfunction (HD) in congenital or tumorous diseases and impact on quality of life.	Manuela Cerbone	Received

273-P3	A rare cause of acute salt wasting crisis in infancy: Case report of Type 1 aldosterone synthase deficiency with CYP11B2 mutation	Ka Yee Chan	Received

273-P2	Post-HSCT Gravess Disease & Autoimmune Hypothyroidism in Toddlers with Severe Combined Immunodeficiency due to RAG1/RAG2 gene mutation: Keep an eye on the thyroid function following HSCT	Ghassan Mohamadsalih	Received

274-P3	Iatrogenic cushings syndrome in infants	Meryem Smouni	Received

274-P1	Somatotropinomas in Pediatric Endocrinology Practice: Single Center Experience	Gözde Gürp;nar	Received

275-P1	Endocrine Deficiency after Photon and Proton Radiotherapy for Medulloblastoma in Hokkaido University Hospital, Japan.	Naoya Kaneko	Received

275-P2	Persistent tachycardia in a teenager with Graves disease on block and replace therapy	Sharon Lim	Received

276-P2	Delusional psychosis in a 14-year old female with Graves Disease	Misako Okuno	Received

276-P3	11 -Hydroxylase deficiency presenting with precocious puberty and gigantism : case report	Hassiba Sahli	Received

277-P2	Atypical Presentation of Childhood Primary Hypothyroidism with Reversible Chronic Kidney Disease stage-2	Ghassan Mohamadsalih	Received

277-P1	A rare cause of hypogonadotropic hypogonadism: KLB gene variant in a prepubertal boy evaluated for micropenis	Zehra Yavas Abali	Received

278-P2	PREDICTIVE FACTORS OF TRANSIENT CONGENITAL HYPOTHYROIDISM: A RETROSPECTIVE STUDY	Lorna Abad	Received

279-P2	Secondary Hypertriglyceridemia Due to Diabetes Mellitus and Hypothyroidism in A Pediatric Patient.	Jamala Mammadova	Received

279-P3	Nutritional rehabilitation in children with idiopathic stunted growth: is it a recovery pattern of growth?	Chaymae HAMDANE	Received

280-P2	Neurodevelopmental Outcome in Children with Congenital Hypothyroidism Between 6 to 42 Months of Age A Cross-Sectional Analytical Study	CG Delhikumar	Received

280-P3	Skeletal Manifestations in Children with Nephropathic Cystinosis- Single Center Experience	Noha Aly	Received

280-P1	Validation Of A New Short Parent-Reported Outcomes (PRO) Questionnaire For Boys With A Condition Affecting Sex Development (CSD)	Xanthippi Tseretopoulou	Received

281-P1	Comparison between, clinical, metabolic and hormonal parameters and ed microRNAs in adolescent girls with PCOS and healthy controls	Vilhelm Mladenov	Received

281-P3	CLEIDOCRANIAL DYSPLASIA ASSOCIATED WITH GH DEFICIENCY BY AUXOLOGICAL CRITERION: CASE REPORT	Ricardo Fernando Arrais	Received

282-P3	Fibrous dysplasia of the bone, a disabling complication of McCune Albright syndrome: a case report	Halima Zerguine	Received

282-P2	THYROID HORMONE PROFILE AND AUTOIMMUNITY IN DOWN SYNDROME	Aylin Günay	Received

282-P1	ESTROGEN AND PROGESTERONE IN IMMUNE DYSFUNCTION AT CHILDHOOD FOLLOW UP OF PRETERM INFANTS	Philip Stewart	Received

283-P3	Bone growth deficits correlated with visceral fat mass volume in adolescent girls with severe and extreme obesity	Veselin Boyadzhiev	Received

283-P1	Care in the first weeks after a suspected DSD diagnosis results of the Empower-DSD information management program	Katja Wechsung	Received

283-P2	Evaluation of thyroid function in a pediatric cohort with chronic spontaneous urticaria: a retrospective, single-center, observational study.	Simone Foti Randazzese	Received

284-P1	Face processing patterns in individuals with gender incongruence or differences of sex development: an eye-tracking study.	Zofia Kolesinska	Received

284-P3	Dramatic deterioration of subclinical hyperparathyroidism in children and adolescents during the post-COVID-19 period	Dimitrios T Papadimitriou	Received

285-P2	Levothyroxine poisoning in children is usually benign: A multi-center experience from Turkey	Kübra Sen Küük	Received

285-P1	A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure	Deniz Özalp K&305;z&305;lay	Received

285-P3	To Study The Risk Factors for Type 1 Diabetes Mellitus Among Children and Adolescents in a Tertiary Care Hospital	Aamir Naseem	Received

286-P2	Five-Year Experience of Diagnosing and Managing Congenital Hypothyroidism through Dried Blood Spot Newborn Screening in Pakistan: A Comprehensive Clinical Profile and Outcome Analysis	Bushra Rehman	Received

286-P1	Impact of COVID-19 on Pediatric Graves Disease: Trends and Insights	Alessandro Naim	Received

287-P3	ABCC8 gene mutations: two mirror reflections	Júlia Galhardo	Received

288-P3	Improving Diagnosis and Management for Type 1 Diabetes Mellitus (T1DM) among Children and Adolescents, through Introduction of First-ever T1DM Management Guidelines in Kenya	Phoebe Wamalwa	Received

288-P2	BRAF mutation in a pediatric patient incidentally discovered with papillary thyroid cancer- case report	Simona Fica	Received

289-P3	Three cases of neonatal diabetes mellitus with different clinical courses	Yasunori Wada	Received

289-P2	What to do for Atypia of Uncertain Significance in Thyroid?	ZULAL OZDEMIR USLU	Received

289-P1	Papillary thyroid cancer in a teenager with thyroid hormone resistance syndrome: features of postoperative management.	Sofia Mikhalina	Received

290-P1	A Retrospective Observational Study of Patients with Differentiated Thyroid Cancer from a Pediatric Endocrinology Clinic in Crete	Lydia Mavraki	Received

290-P3	The Impact of Insulin-Induced Lipodystrophy on Glycemic Variability in Pediatric Patients with Type 1 Diabetes	hanae bakmizi	Received

290-P2	Graves disease in children and adolescents, results of a multicenter Algerian study	MERYEM BENSALAH	Received

291-P3	Safety and Metabolic Outcomes of Medtronic Minimed 780G Initiation at Diagnosis in Children and Adolescents	Ugur Cem Yilmaz	Received

291-P1	Response to TRIAC therapy in a child with Resistance to Thyroid Hormone beta and behavioural abnormalities.	Anand Ramakrishnan	Received

292-P2	Normal Thyroid Gland Size in Healthy Turkish Newborns Living In An Iodine-Sufficient Area: Ultrasonographic Measurements and Comparison of Handheld and Standard Devices	reyhan deveci sevim	Received

292-P1	Congenital autoimmune thyreoiditis with hypothyroidism: first expression of a STAT-3-associated multisystemic disease with further severe autoimmune manifestations	Ourania Ververidou	Received

292-P3	Is the diary for self-monitoring of blood glucose levels in children with diabetes reliable?	Ahmed Salih Bendeddouche	Received

293-P3	Impact of Ramadan fasting on young people with diabetes type 1	Ahmed Salih Bendeddouche	Received

293-P1	Genetic Etiology in Congenital Hypothyroidism	Gözde Gürpinar	Received

293-P2	Prevalence and Predictor Factors of Transient Congenital Hypothyroidism in Resource-limited Setting	ABRAHAM PAULOSE	Received

294-P3	Hepatic glycogenosis in poorly controlled type 1 diabetics: four case reports	Halima Zerguine	Received

294-P1	Prolacrin associates to adrenal androgens during adrenarche	Veronica Mericq	Received

295-P2	Graves Disease in Children and Adolescents: A 10 years retrospective analysis of patients followed in a Single Center	Eleni Gkougkouli	Received

295-P1	GC-MS urinary steroid metabolome reveals substantial dysregulation of adrenal, gonadal, and neuroactive steroids in adolescents with depressive symptoms	Lars Dinkelbach	Received

295-P3	Psychological evaluation in children and adolescents with diabetes mellitus	Jeesuk Yu	Received

296-P2	Treatment with Continuous Subcutaneous Hydrocortisone Infusion (CHSI) in Children with congenital adrenal hyperplasia (CAH) due to 21 hydroxylase deficiency : An Option for Poorly Controlled Patients	anne sophie lambert	Received

296-P1	Evaluating Setmelanotide Treatment for 12 Months in Pediatric Age Groups With Rare Melanocortin-4 Receptor PathwayRelated Obesity: Efficacy in Weight Reduction and Safety Outcomes	Vaishali Kakkar	Received

296-P3	Circumstances of diagnosis of type 2 diabetes in children and young adolescents	Foued Abdelaziz	Received

297-P1	Three-year results on weight and eating disorders with digi-physical treatment in paediatric obesity: A pragmatic clinical trial	Louise Lindberg	Received

297-P3	THYROID FUNCTION AND AUTOIMMUNITY IN CHILDREN TYPE I DIABETES	AMAL OURDI	Received

298-P3	NUTRITIONAL DEFICIENCIES AND ENDOCRINE DYSFUNCTION INCHILDREN WITH TYPE 1 DIABETES AND CELIAC DISEASE	AMAL OURDI	Received

298-P1	The severity and correlates of depressive symptoms in adolescents with obesity compared to normal adolescents in Hong Kong using a validated Patient Health Questionnaire-9 screening tools.	Wing Shan See	Received

298-P2	A real-world data analysis of 37 pediatric patients with pheochromocytoma and paraganglioma: Evaluation of the concordance between current diagnostic and treatment algorithms and clinical management practices in resource-limited settings	Ilknur Kurt	Received

299-P3	Coexistence of Autoimmune Disorders in children newly diagnosed with Type 1 Diabetes Mellitus	Nihad SELIM	Received

299-P1	A Real-World Pharmacovigilance Assessment and Literature Review of Lymphoma Development in Lipodystrophy and Congenital Leptin Deficiency	Rebecca J. Brown	Received

299-P2	A novel mutation in type 1 familial glucocorticoid deficiency associated with a deletion of chromosome 9	sakina kherra	Received

300-P2	Comparison of Steroid Hormone Levels Measured by Immunoassay and Liquid Chromatography-Mass Spectrometry (LC-MS) Methods in the Follow-Up of Patients with Congenital Adrenal Hyperplasia	Elif Özsu	Received

300-P3	Predictive factors of diabetic ketoacidosis in children with newly onset type 1 diabetes: A single center study	Nihad SELIM	Received

300-P1	The Diagnostic and Therapeutic Monitoring Value of Morning Urinary Gonadotropins for Central Precocious Puberty in Girls with Different BMI	Wenyong Wu	Received

301-P2	Use of a F-Dex Binding Assay to Determine Steroid Response in Patients with Congenital Adrenal Hyperplasia	Javier Aisenberg	Received

301-P3	Eosinophilic esophagitis and type 1 diabetes: a case report	BELLA Houda	Received

301-P1	The incidence of central precocious puberty and the Role of BMI (real-world data In Korea)	In Hyuk Chung	Received

302-P1	Evaluation of Copeptin Level in Children and Adolescents Monitored with Central Diabetes Incipidus	Elif Ozsu	Received

302-P3	Glycated hemoglobin in diabetes screening: attention to false positives	Hassiba Sahli	Received

303-P2	Copy number variations from whole exome sequencing in children with skeletal dysplasia	Takuo Kubota	Received

304-P2	Basal Ganglia Calcification in Children with Hypoparathyroidism and Pseudohypoparathyroidism: Characterization of Relationships and Clinical and Laboratory Findings	Busra Gurpinar Tosun	Received

304-P1	ER stress relief drives -cell proliferation	Willem Staels	Received

305-P2	Clinical Evaluation and Molecular Analysis of Genetic and Epigenetic Inactivation Defects in GNAS in children: A multicenter experience in China	Wei Wu	Received

305-P1	Lipodystrophy severity score improves in patients with generalized lipodystrophy following metreleptin treatment	Rebecca Brown	Received

306-P2	GENOTYPE AND CLINICAL CHARACTERISTICS ANALYSIS OF NINETEEN CHINESE SHORT-STATURE PATIENTS WITH ACAN GENE VARIANTS	Hong Chen &38472;&29790;&25935;	Received

306-P3	A Rare Cause of Early-Onset Obesity: A Novel Variant in LEPR	Murat aglar Karatas	Received

306-P1	Role of Cubulin gene variants in the development of microalbuminuria in children with type1 diabetes	Noha Arafa Mohamed Hussein Aly	Received

307-P2	An Observational Study to evaluate levels of Alkaline Phosphatase in Boys with Duchenne Muscular Dystrophy in South Wales.	Anshika Singh	Received

307-P3	Disorders of the Melanocortin Pathway: From Genetic Inheritance to Clinical Manifestations Based on a Family Case Study	Anna St&281;pniewska	Received

307-P1	The man in the LOOP: Ramadan fast in Type 1 diabetic patients with a Closed Loop automated insulin delivery system	Yonatan Abraham Schuldenfrei	Received

308-P2	A Novel homozygous founder mutation in UFSP2 is associated with a distinct form of skeletal dysplasia in Emiratis	Manal Mustafa	Received

308-P3	Studying the correlation between leptin hormone and body mass index in children with alimentary obesity	Aysel SULEYMANLI	Received

308-P1	Empowering diabetes self-management and peer connections The role of a community young adult diabetes specialist nurse (CODSN) and diabetes youth worker (YW) in improving outcomes, Transition Safe and Sound (TraSS), an NHS England pilot.	Kelly Carden	Received

309-P3	Metreleptin dramatically improves the metabolic pattern in a patient with mandibuloacral dysplasia progeroid syndrome (MADaM).	Viola Trevisani	Received

309-P2	Inadequate immune response post- vaccination and recurrent bacterial infections in a patient with X-linked hypophosphatemia, resolved under Burosumab therapy	Diana-Alexandra Ertl	Received

309-P1	Safety and efficacy of efpegerglucagon in patients with congenital hyperinsulinism: interim results from a phase 2 study	EunJi Gwak	Received

310-P2	Hypervitaminosis D-induced hypercalcemia in infants: just a simple intoxication?	Carlo Mariani	Received

310-P1	The iPhone Measure app as a measuring device for the height in pediatrics: a reliability study	Reham Ghanim	Received

311-P2	Genotype and phenotype characteristics and long-term follow-up of patients with Vitamin D Dependent Rickets Type II (VDDRII): A nationwide multicenter retrospective cross-sectional study	Huseyin Demirbilek	Received

311-P1	Heterozygous PLAG1 gene variants causing Silver-Russell syndrome in a case series of 4 patients	Alicia Juriaans	Received

312-P3	Association between Small for Gestational Age and Mental Disorders: A Systematic Review and Meta-Analysis	Anran Tian	Received

312-P2	Infantile Hypercalcemia Type 2 due to a novel compound heterozygous association in the SLC34A1 gene in a neonate with hypercalcemia and nephrocalcinosis	Dimitrios T Papadimitriou	Received

312-P1	SGPL1 deficiency is associated with reduced lipid droplet formation and impaired steroidogenesis in Leydig cells	Ruth Kwong	Received

313-P1	Do We Need Seasonal Thyroid Hormone Reference Values in Pediatric Endocrinology? Results from a Population-Based Study	Raphael Hirtz	Received

313-P3	Bartter Syndrome Type 2 presenting as transient pseudohypoaldosteronism with hypocalcaemia: a diagnostic dilemma unveiled by genetic testing	Jananie Suntharesan	Received

313-P2	Correlation of Bone Health Index (BHI) and Metacarpal Index (MCI) with calcium metabolism parameters in children and adolescents	Dimitrios T Papadimitriou	Received

314-P2	Bone Health Index (BHI) and Metacarpal Index (MCI) in boys and girls on treatment with aromatase inhibitors	Dimitrios T Papadimitriou	Received

314-P3	MRI Structural and Functional Changes in Children with Growth Hormone Deficiency: A Chronological Review	FAWZIYA ALYAFEI	Received

315-P3	Prevalence and Clinical Associations of Functional Brain Changes in Children with Growth Hormone Deficiency: A Comprehensive Review	FAWZIYA ALYAFEI	Received

315-P2	SEMAGLUTIDE MODULATED THE GUT MICROBIOME COMPOSITION AND IMPROVED BILE ACID PROFILES IN A MOUSE MODEL OF DIABETIC NEPHROPATHY	Huimin Kang	Received

316-P3	Functional Magnetic Resonance Imaging (fMRI) Findings and Brain Maturity Index in Children with Idiopathic Short Stature and Growth Hormone Deficiency: A Comprehensive Review	Ashraf Soliman	Received

316-P2	A critical role for iron import through the transferrin receptor in developing -cells.	Willem Staels	Received

317-P2	A case of A20 haploinsufficiency and type 1 diabetes mellitus in an infant	Daiki Kondo	Received

317-P3	Genetic Findings in Growth Hormone Deficiency and Idiopathic Short Stature: A Comprehensive Review	Ashraf Soliman	Received

318-P2	Levels of NK cells in a cohort of Bulgarian children with type 1 diabetes	Stanimira Elkina	Received

319-P2	Sex, age and irisin levels in pediatric type 1 diabetes: a pilot study	Shay Averbuch	Received

319-P3	Relevance of the hypoglycemic insulin stimulation test in 486 cases	Ahmed Salih Bendeddouche	Received

320-P2	Screening for celiac disease in children and adolescents with type 1 diabetes, what to do?	Ana Pilar Achón Buil	Received

320-P3	PREDICTIVE FACTORS OF PERSISTENT GH DEFICIENCY AND IMPACT ON THE FINAL HEIGHT: A RETROSPECTIVE COHORT STUDY	FLAVIA URBANO	Received

321-P2	Lipid lowering therapy, LDL- and non-HDL-cholesterol in children and adolescents with type 1 diabetes: An analysis based on the DPV registry	Marianne Becker	Received

321-P3	ETIOLOGICAL ASPECTS OF GROWTH FAILURE	Benyahya Nadia	Received

322-P2	Mauriac syndrome: A rare complication of Type 1 Diabetes Mellitus	Sona Samvelyan	Received

322-P3	Evaluation of Effects of Using Mobile Treatment Reminder GroConnect on Treatment Compliance and Treatment Response in Patients Receiving Growth Hormone Treatment Preliminary Results	Tu&287;e Kandemir	Received

323-P2	Hypoglycemia and type 2 diabetes mellitus in a patient with endogenous high methanol and his follow up	Maryam Razzaghy Azar	Received

323-P3	Etiology and characteristics of children with short stature in endocrinology department	Samira Azzoug	Received

324-P2	HOMA and Matsuda Index as Screening Tests for Cystic Fibrosis Associated Diabetes in Children	Serpil Albayrak	Received

325-P2	A novel mutation of CGK gene in patient with Diazoxide responsive congenital hyperinsulinism	Sakina Kherra	Received

325-P3	Prevalence and Degree of Structural Changes in Children with Growth Hormone Deficiency: A Comparative Review with Idiopathic Short Stature	FAWZIYA ALYAFEI	Received

326-P3	Effect of IM Depot Estradiol on Pubertal Progression and Uterine Development in Turner Girls	Ghada Anwar	Received

327-P2	A myostatin inhibitory antibody potentiates the positive effects of insulin on the skeletal muscle and bone phenotype of insulin-deficient diabetic female mice	Evangelia Kalaitzoglou	Received

327-P3	Novel homozygous RTTN variant causing post-natal microcephaly, dwarphism, intellectual delay and micropenis: a case report.	Francesca Aiello	Received

328-P3	Temple syndrome; genetics and characteristics	Raihana Hashim	Received

329-P3	TURNER SYNDROMES MALFORMATIVE AND AUTOIMMUNE PROFILE	Nadia Benyahya	Received

329-P2	Metformin May be Sufficient to Control Glycemia and Delay Insulin Dependency in Obese Youth Presenting with Type 1 DM: A Report of 3 Patients	Bayan Alnassir	Received

330-P3	PHOSPHOCALCIC PROFILE AND ORTHOPEDIC MANIFESTATIONS IN TURNER SYNDROME	Hanae Rachedi	Received

331-P2	Impact of Diabetes Mellitus on Growth of the Affected Children and Young People - Single Centre Experience from Oman	Hussain Alsaffar	Received

331-P3	Associated clinical abnormalities among patients with Turner syndrome	Nihad SELIM	Received

332-P3	Chest Physiotherapy and Growth in preadolescents Algerians Children with Cystic Fibrosis : The Experience of a single center.	Meriem OUSSALAH	Received

333-P2	Accelerated growth of preadipocyte cultures with TSC1 downregulation might be linked to lipoma development and can be reversed by mTOR or PI3K inhibition	Anna Kirstein	Received

333-P3	Fahrs Disease presenting with nonfebrile epileptic seizures: Case report and Systematic Literature Review	Abdelilah Radi	Received

334-P3	A Case of 21-Hydroxylase Deficiency with Familial Hypercholesterolemia	Ruimin Chen	Received

334-P2	Predicting metabolically unhealthy obesity in children	Anna Nikulina	Received

335-P2	Exploring the clinical outcomes and experiences for young people (12-17) taking Liraglutide for weight loss	Natasha Schaefer	Received

336-P2	The Role of Spexin in Metabolic Syndrome Among Childhood Obesity	Duygu Y&305;lmaz	Received

337-P3	CSNK2B mutation: a rare cause of IGHD	karine aouchiche	Received

337-P2	ABETALIPOPROTEINEMIA: A CASE REPORT	Ricardo Fernando Arrais	Received

338-P3	Diagnostic Accuracy of ITT Peak Cortisol Levels for Identifying ACTH Deficiency in Patients with Suspected Hypothalamic-Pituitary-Adrenal (HPA) Axis Dysfunction.	Sami Alanazi	Received

339-P3	A case of germinoma presented with primary amenorrhae and hypopitutarism	Loan Huynh Thoai	Received

339-P2	Adipose tissue Ago2-deficiency improves obesity-related body fat distribution and metabolic disorders by reducing miRNA production and promoting BCAA catabolism	Qing Li	Received

340-P3	Pituitary stalk interruption syndrome: Clinical, biological and radiological aspects of 20 cases.	meryem smouni	Received

340-P2	Evaluating the efficacy of the Evira treatment for childhood obesity treatment-a 26- week single arm interventional study in Abu Dhabi, United Arab Emirates	Reem Hassan-Beck	Received

341-P2	Risk factors for common obesity among primary school pupils in Batna (Algeria)	Halima Zerguine	Received

342-P2	3-Month real-world setmelanotide hunger and weight outcomes in four French paediatric patients with acquired or congenital hypothalamic obesity	Vaishali Kakkar	Received

342-P3	Growth hormone deficiency and malformative diseases of the pituitary gland: diagnosis and evolutionary particularities in a series of 20 cases	Halima Zerguine	Received

343-P3	Primary amenorrhea in a 16-year-old girl	fadel asma	Received

344-P3	Effects of probiotic supplementation during childhood on the gut microbiota when puberty onset in lactating female mice	Ruimin Chen	Received

344-P2	Fluorescence-Guided Laparoscopic Near-Total Pancreatectomy: An Innovative Approach for Infants with Diffuse Congenital HyperinsulinismA Case Series	Elham Atiq	Received

345-P2	Association between maternal and fetal Small Chain Fatty Acids and offspring anthropometry during the first year of life in pregnancies with GDM: MySweetheart study	Maria-Christina Antoniou	Received

345-P3	An extraordinary case , leydig cell tumor in a 6- year - old girl with significantly elevated 17 - OHP	Esraa Shatnawi	Received

346-P2	Dynamic changes in exocrine pancreatic function after near total pancreatectomy in CHI Patients with KATP channel genes variants	ELPINIKI BEKA	Received

347-P3	A case report of Gonadoblastoma in Turner Syndrome	Sibel Baykut	Received

348-P3	A phenotipically female child with Deletion 9p Terminal Syndrome with Sexual Development Disorder - case report	Milica Ignjatovic	Received

349-P2	Correlation of Pituitary Volume/Size/Height with Clinical Factors in Growth Hormone Deficiency Patients: A Comprehensive Review	FAWZIYA ALYAFEI	Received

350-P2	THE GENETIC AND CLINICAL ASPECTS OF 10 PATIENTS WITH GH-IGF-1 AXIS GENE VARIANTS	xiaozhen &40644;	Received

350-P3	An unusual presentation of longstanding Hashimotos Hypothyroidism with atrophic thyroiditis: Diagnostic challenges and opportunities in a resource poor set up.	Phoebe Wamalwa	Received

351-P2	Up to 5 years of once-weekly somatrogon treatment in pediatric patients with growth hormone deficiency: results from an open-label extension of a global Phase 3 study	Lawrence Silverman	Received

351-P3	Physical and neuropsychiatric development of children with subclinical congenital hypothyroidism does not depend on treatment tactics	Nina Makretskaya	Received

352-P2	Predictive factors for growth hormone response in the first year of treatment among children with growth hormone deficiency in Algeria	sakina kherra	Received

352-P3	PEDIATRIC HASHIMOTOS ENCEPHALOPATHY PRESENTING AS SUPER REFRACTORY STATUS EPILEPTICUS	Anjumanara Omar	Received

353-P3	A rare case of thyroid cancer in an adolescent girl	Wing Shan Queenie See	Received

353-P2	Association between isolated growth hormone deficiency and Jansen de Vries Syndrome: a case report from a Romanian Paediatric Endocrinology Department	Bogdan Pascu	Received

354-P2	The IGF1 generation test as a tool to predict growth response to growth hormone treatment in children with growth hormone deficiency	Sakina Kherra	Received

355-P2	A new score for the diagnosis of Growth hormone deficiency in prepubertal children	ADEL DJERMANE	Received

356-P2	Severe oedema during treatment with long acting GH	Matthias Börschel-Thomsen	Received

357-P2	Real-world IGF-1 Variations & Its Management in Children on Recombinant Human Growth Hormone (rhGH) Therapy (RIGHT Study)	Suet Ching Chen	Received

358-P2	Cross-sectional Insights into the Effects of Heavy Metal Mixtures on Height among Korean Preschoolers: Findings from the Korean National Environmental Health Survey Cycles 3 and 4	Shine-Hye Kim	Received

359-P2	High Frequency of Copy Number Variations as Genetic Causes of Failure to Achieve Catch-Up Growth in Small for Gestational Age Children: A Multicenter Study in Korea	Yena Lee	Received

360-P2	Bone Healt in young patients with Turner Syndrome: crossectional and longitudinal retrospective data.	Emilio Casalini	Received

361-P2	Assessment of Growth Hormone Treatment in Korean Pediatric Growth Disorders: 11-Year Interim Analysis from the LG Growth Study	Yong Hee Hong	Received

364-P2	The Influence of puberty timing on the development of metabolic Syndrome in Turner Syndrome patients.	latifa yagoubi	Received

365-P2	The Diagnostic Yield of Whole Exome Sequencing in Idiopathic Short Stature	Sara Aljazaeri	Received

366-P2	The genomic landscape of children with short stature presenting to a tertiary hospital in UAE.	ANJU JACOB	Received

367-P2	A Novel Case of Lipoatrophy Due to a Non-Pegylated Long-Acting Growth Hormone Somatrogon	And Demir	Received

368-P2	Unusual presentation of Wolfram syndrome in children with urinary tract dysfunctions.	Nino Abdushelishvili	Received

369-P2	Management challenges of an infant with multiple endocrinopathies with McCune Albright Syndrome: A Case Report	Jananie Suntharesan	Received

371-P2	An exploration of a data visualisation web application for rare disease registries.	Krish Panchigar	Received

372-P2	Caregiver-reported quality of life of patients with MCT8 deficiency: results from a cross-sectional survey	Akosua Ofori	Received

374-P2	Analysis of serum microplastics in girls with precocious puberty and its correlation with steroid hormones	Xiaoqin Yin	Received

376-P2	Central Precocious Puberty and MKRN3 variants: new insights into the protein RING finger structure, and on protein ubiquitination and localization	Anna Grandone	Received

377-P2	The etiology of Central Precocious Puberty and the Impact of Gonadotropin-Releasing Hormone Agonist Therapy: Albanian experience.	Agim Gjikopulli	Received

378-P2	Serum vascular endothelial growth factor-A (VEGF-A) levels regarding pubertal stage and obesity in girls	Hyo-Kyoung Nam	Received

381-P2	A Novel and Validated Noninvasive Method for Determining the Onset of Biochemical Puberty and Predicting Imminent Clinical Puberty	And Demir	Received

382-P2	Testosterone Replacement Therapy in adolescents and young adults with Prader-Willi Syndrome: Efficacy and effects on behaviour	Demi Trueba - Timmermans	Received

383-P2	Transcriptome Analysis of Adult Females Previously Affected by Central Precocious Puberty due to DLK1 Mutations	Candy Christie Bellido More	Received

385-P2	Integrating Genetic Testing in the Evaluation of Boys with Central Precocious Puberty: A Portuguese Nationwide Study	Elisa Galo	Received

386-P2	Insulin resistance is frequent in non-obese adolescent girls with irregular menstruation and/or clinical hyperandrogenism	Deniz Erden Firat	Received

387-P2	Development and validation of central precocious puberty diagnostic prediction models in girls based on machine learning	Wenyong Wu	Received

388-P2	IRS-1 as a key point in the regulation of insulin-sensitivity in granulosa cells from PCOS women.	Chiara Sartori	Received

389-P2	A comprehensive overview of the changes in IGF system peptides in the follicular fluid (FF) of women with Polycystic Ovarian Syndrome (PCOS) and their relationships with BMI and HMGB1	Chiara Sartori	Received

390-P2	Histological Progression and Malignancy Risk in 17-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Insights from Infancy to Adulthood	Yunpeng Wang	Received

391-P2	QT Interval Dynamics in Transgender/Gender diverse Adolescents on GnRHa and Gender-Affirming Hormonal Therapy: A Comparative Analysis	Hussein Zaitoon	Received

392-P2	Identification of Three Novel PPP1R12A Variants From Whole Genome Sequencing in Individuals with Differences of Sex Development (DSD)	Gabby Atlas	Received

393-P2	Transcriptomic analysis of peripheral blood mononuclear cells reveals immune and metabolic pathways associated with both puberty-blockade and gender-affirming sex hormone therapy in healthy young transgender individuals	Heather Cross	Received

395-P2	Development of Age-Adapted Modules for Standardized Clinical Data Collection in individuals with Klinefelter Syndrome	Corinna Grasemann	Received

398-P2	Orbital myositis revealing TRAb negative Gravesdisease : an exceptional situation	Ouamer Ould Mohand	Received

399-P2	Mutations in THRB gene are associated with combined congenital hypothyroidism and TSH resistance.	Mohammad Awad	Received

401-P2	Euthyroid graves ophtalmopathy in an adolescent sero-negative for TSH receptor autoantibody : a case report	Latifa Sifour	Received

402-P2	Evaluation of clinical characteristics and genotype-phenotype correlation of resistance to thyroid hormone receptor Beta (RTH) due to THR gene mutations	Huseyin Demirbilek	Received

The 62nd Annual ESPE Meeting 2024

November 16 – November 18 Liverpool

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