Previous issue | Volume 92 | ESPE2019

58th Annual ESPE meeting

Vienna, Austria
19 Sep 2019 - 21 Sep 2019

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The theme of this year’s meeting is Variety and Variation in Paediatric Endocrinology. Join us in Vienna to explore the diversity we encounter in our discipline and the care that we have to exercise when using the term “normality”. Whilst gaining an update on the latest treatments, clinical best practice and cutting edge research in the field of paediatric endocrinology.

Poster Category 2

Growth and Syndromes (to include Turner Syndrome)

The Impact of Growth Hormone Treatment in Patients with Noonan Syndrome and Growth Hormone Deficiency
1Ajou University Hospital, Suwon, Korea, Republic of. 2Korea Cancer Center Hospital, Seoul, Korea, Republic of
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Efficacy and Safety of Growth Hormone (GH) in the Treatment of Children with Hypochondroplasia (HCH): Comparison with a Historical Cohort of Untreated Children with HCH
1Hôpital Universitaire Necker Enfants Malades, Pediatric Endocrinology and Diabetes, Paris, France. 2IMAGINE Institute, Medical Genetics Department, Paris, France. 3Merck s.a.s, Lyon, France. 4Hôpital Necker Enfants Malades, Physiology Laboratory, Paris, France. 5CNRS FRE2029, Paris, France. 6Université Paris Descartes, Paris, France
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Five Novel Variants of KMT2D/KDM6A Found in Seven Chinese Patients with Kabuki syndrome and a Literature Review of 39 Patients Reported in China
1Fuzhou Children's Hospital of Fujian Province, Fujian Medical University Teaching Hospital, Fuzhou, China. 2The Capital Medical University Affiliated Beijing Children Hospital, Beijing, China. 3Shanghai Children's Medical Central Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China
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Adult Height of Patients Enrolled in PATRO Children, An Ongoing Observational Study of the Long-term Safety And Effectiveness Of Omnitrope®
1Department of Paediatrics, Royal Alexandra Children's Hospital, Brighton, United Kingdom. 2Division of Pediatric Endocrinology, Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, Ohio, USA. 3Department of Pediatrics and Adolescence Medicine, University Hospital Freiburg, Freiburg, Germany. 4Pediatric Endocrinology, Ospedale Pedatrico Microcitemico 'A. Cao' - AOB Cagliari, Cagliari, Italy. 5Sandoz GmbH, Holzkirchen, Germany
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A Novel Case Of Paternal Isodisomy for Chromosome 7 Associated with Overgrowth
1Medical Genetics Unit, Department of Clinical and Experimental Biomedical Sciences 'Mario Serio', University of Florence, Florence, Italy. 2Medical Genetics Unit, Meyer Children's University Hospital, Florence, Italy. 3Division of Pediatric Endocrinology, Meyer University Children's Hospital, University of Florence, Florence, Italy
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Auditory Phenotypes and Dynamics of Hearing Thresholds in 246 Turner Syndrome Females
1Pediatric Unit, Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy. 2Otorhinolaryngology Unit, Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy. 3Rare Diseases and Auxological Unit, Department of Pediatrics, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy. 4Department of Economics, Unit of Statistics and Mathematical Sciences, University of Messina, Messina, Italy
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Effect of Gonadotropin-Releasing Hormone Agonists on Auxological Outcomes of Korean Boys with Central Precocious Puberty and Early Puberty
1Ajou University Hospital, Suwon, Korea, Republic of. 2Korea Cancer Center Hospital, Seoul, Korea, Republic of
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"Transition Readiness in Girls and Young Women with Turner Syndrome – are they Less Ready?" Associations between Transition Readiness and Diagnosis
1Medical University of Vienna, Vienna, Austria. 2Medical University of Graz, Graz, Austria. 3 Sozialmedizinisches Zentrum Süd - Kaiser-Franz-Josef-Spital mit Gottfried von Preyer'schem Kinderspital, Vienna, Austria. 4Medical University of Graz, Vienna, Austria
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The First Case of Genetically Diagnosed Cantu´ Syndrome in China with Mutation in ABCC9
Department of Pediatrics, the Second Xiangya Hospital, Central South University, Changsha, China
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Shox-Haploinsufficiency Intra-Familial Phenotipic Variability and the Impact on Final Height: Report of a Pedigree
1Department Promise "G. D'Alessandro", University of Palermo, Palermo, Italy. 2UOC IV Pediatria, Children Hospital "G. Di Cristina", ARNAS, Palermo, Italy
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Growth Hormone Treatment Adherence in Patients from an Emerging Economy Country: 1-Year Real-World Data from the Easypod™ Connect Ehealth Platform
1Assistant Professor. Santa Casa de São Paulo School of Medical Sciences, São Paulo, Brazil. 2Merck Brazil, a business of Merck KGaA, Darmstadt, Germany. 3Merck KGaA, Darmstadt, Germany
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The Clinical Features and Effect of Growth Hormone Treatment in 3-M Syndrome Cases with Severe Growth Retardation
1Istanbul University, Istanbul Faculty of Medicine, Department of Pediatrics, Pediatric Endocrinology Unit, Istanbul, Turkey. 2Istanbul University, Istanbul Faculty of Medicine, Department of Medical Genetics, Istanbul, Turkey
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Klinefelter Syndrome Associated with Short Stature Due to Iatrogenic Cushing
1Federal University of Goiás, Goiânia, Brazil. 2Replicon Genetic Research Group, Goiânia, Brazil
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Extending the Phenotype and Genotype of Okur–Chung Neurodevelopmental Syndrome
Department of Pediatrics, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, GuangZhou, China
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Evaluation of Diagnosis, Follow-up and Treatment Results of Growth Hormone in Rare Diseases; 10 Year Single Center Experience
1Ankara University Medicine Faculty, Pediatric Endocrinology Department, Ankara, Turkey. 2Dr.Sami Ulus Maternity, Child Health and Diseases Training and Research Hospital, Pediatric Endocrinology Department,, Ankara, Turkey
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Growth failure in children with sickle cell anemia
1University of Nigeria, Ituku Ozalla, Enugu, Nigeria. 2University of Nigeria,Ituku Ozalla, Enugu, Nigeria
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Endocrine Features of Schaaf-Yang Syndrome. Case Report
Dnipropetrovsk Medical Academy, Dnipro, Ukraine
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The Applicability of the NH-Clinical Scoring System on Diagnosis of Iranian Children with SRS
1Pediatric endocrinology wards,Mashhad and Sabzevar University of Medical Sciences, Mashhad - Sabzevar, Iran, Islamic Republic of. 2Pediatric endocrinology wards,Mashhad University of Medical Sciences, Mashhad, Iran, Islamic Republic of. 3Medical genetic research center,Mashhad university of medical sciences, Mashhad, Iran, Islamic Republic of
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