58th Annual ESPE meeting
Vienna,
Austria
19 Sep 2019 - 21 Sep 2019
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 1
Growth and Syndromes (to include Turner Syndrome) (2)
Growth Hormone Deficiency (GHD): Assessing Parent Burden for Child Growth Hormone Deficiency Treatment: The Growth Hormone Deficiency - Parent Treatment Burden Measure (GHD-PTB)
1The Brod Group, Mill Valley, USA. 2Novo Nordisk A/S, Søborg, Denmark
hrp0092p1-371
A Considerable Role of NPR2 Mutation in Idiopathic Short Stature: Identification of Two Novel Mutations
1Kangdong Sacred Heart Hospital, Seoul, Korea, Republic of. 2Sanbon Medical Center, Wonkwang University, Gyunggi, Korea, Republic of. 3Chosun University Hospital, Gwangju, Korea, Republic of
hrp0092p1-372
Matrix Metalloproteinases, their Inhibitors and Neurotrophic Factors as Indicators of Cardiometabolic Risk in Turner Syndrome Girls
1Department of Pediatrics and Pediatric Endocrinology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland. 2Students' Scientific Association at the Department of Pediatrics and Pediatric Endocrinology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland. 3Department of Biochemistry, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland
hrp0092p1-373
Growth in the First Ten Years after Antiretroviral Therapy Initiation Among HIV-Infected Children in the CoRISpe Spanish Pediatric Cohort.
Riscart Jesus Dominguez
Montojo Fatima Ara
Garcia Luis Escosa
Costa Talia Sainz
Casado Isabel Gonzalez
1Hospital Universitario La Paz. Servicio de Endocrinologia infantil, Madrid, Spain. 2Hospital Universitario La Paz. Servicio de Infectologia Pediátrica, Madrid, Spain
hrp0092p1-374
SOAR Study: New Approaches to Managing Social Skills Deficits in Turner Syndrome
1UCL GOS Institute of Child Health, London, United Kingdom. 2UCL, London, United Kingdom
hrp0092p1-375
Noonan Syndrome (NS) Spectrum Panels should Include Mutations in LZTR1 Gene
Güemes Maria
Martín-Rivada Álvaro
Ortiz-Cabrera Nelmar Valentina
Martos-Moreno Gabriel Ángel
Pozo-Román Jesús
Argente Jesús
1Department of Pediatrics & Pediatric Endocrinology, Hospital Infantil Universitario Niño Jesús, Universidad Autónoma de Madrid, Madrid, Spain. 2Hospital de la Princesa Research Institute, Madrid, Spain. 3Clinical Genetics Service, Hospital Infantil Universitario Niño Jesús, Universidad Autónoma de Madrid, Madrid, Spain. 4Centro de Investigación Biomédica en Red de Fisiopatologia de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, Madrid, Spain. 5IMDEA Food Institute, CEI UAM + CSIC, Madrid, Spain
hrp0092p1-376
International Consensus: Ovarian Tissue Cryopreservation in Young Turner Syndrome Patients. Outcomes of an Ethical Delphi Study Including 55 Experts from 16 Different Countries.
Schleedoorn Myra
Mulder Bjarne
Braat Didi
Beerendonk Catharina
Peek Ron
Nelen Willianne
van Leeuwen Evert
van der Velden Janielle
Fleischer Kathrin
Radboud university medical centre, Nijmegen, Netherlands
hrp0092p1-377
Vascular Anomalies and Aortic Dilatation in Turner Syndrome Study in a Large Cohort of Young-Adult Patients
Scarano Emanuela
Varini Susanna
Tamburrino Federica
Perri Annamaria
Costa Margherita
Prandstraller Daniela
Lovato Luigi
Balducci Anna
Gibertoni Dino
Mazzanti Laura
1Rare Unit Disease, Department of Pediatrics, St. Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy. 2Pediatric Cardiology GUCH Unit, Cardiothoracic-Vascular Department, St. Orsola-Malpighi University Hospital, University of Bologna,, Bologna, Italy. 3 Cardiology, Department of Experimental Diagnostic and Specialty Medicine, St. Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy. 4Department of Biomedical and Neuromotor Sciences, Unit of Hygiene and Biostatistics, University of Bologna, Bologna, Italy
hrp0092p1-378
Adult Height Prediction by Bone Age Determination in Children with Idiopathic Growth Hormone Deficiency (IGHD): Analysis of KIGS Data
1Pediatric Endocrinology, Diabetes and Nutrition Medicine, Vestische Children's Hospital, University of Witten/Herdecke, Datteln, Germany. 2Endocrine Care, Pfizer Inc., New York, NY, USA. 3Division of Pediatric Endocrinology, University of Patras, Patras, Greece
hrp0092p1-379
A New Model of Adult Height Prediction Validated in Boys with Constitutional Delay of Growth and Puberty
1Vesitsche Children`s Hospital, Datteln, Germany. 2Vesitsche Children`s Hospital, Datteln, Ghana. 3Children`s Hospital, Tübingen, Germany
hrp0092p1-380
The Relation Between Changes in Body Mass Index (BMI) and Linear Growth in Prepubertal Children: Daily Weight Gain and BMI Changes in Relation to Linear Growth During Nutritional Rehabilitation of Underweight Children.
Soliman Ashraf Tawfik
Itani Maya
Jour Celine
Shaat Mona
Elsiddig Suhair
Souieky Fatima
Al-Naimi Noora
Hamad General Hospital, Doha, Qatar
hrp0092p1-381
Nutritional Requirements in Prader Willi Syndrome Children Treated with Growth Hormone Under Two Years of Age
Corripio Raquel
Franch Noemi
Couto Yolanda
Pérez Jacobo
Gabau Elisabeth
Capdevila Nuria
Rivera Josefa
1Parc Tauli Sabadell, Hospital Universitari, Sabadell, Spain. 2University Autonomous Barcelone, Bellaterra, Spain
hrp0092p1-382
Cardiovascular Anomalies and Association with Karyotypes in Turner Syndrome in Taiwan: One Medical Center Experience
Chang Gung Memorial Hospital, Taoyuan, Taiwan
hrp0092p1-383
Pubertal Induction Amongst Girls with Turner Syndrome: A Review of Changing Practice Over 10 Years.
1University of Maiduguri, Maiduguri, Nigeria. 2Nottingham University Hospital, Nottingham, United Kingdom
hrp0092p1-384
Saliva Might be a Good Alternative DNA Source for Whole Exome Sequencing to Identify Genetic Causes of Short Stature
1Pusan National University, Yangsan, Korea, Republic of. 2Pusan National University, Yangsan, Lao, People's Democratic Republic. 3MIRAE CHILDREN'S HOSPITAL, Pusan, Korea, Republic of. 4ILSIN CHRISTIAN HOSPITAL, Pusan, Korea, Republic of
hrp0092p1-385
Prevalence of Copy Number Variations (CNVs) in a Cohort of SGA Children with Persistent short Stature Associated with Additional Clinical Features.
Inzaghi Elena
Deodati Annalisa
Bizzarri Carla
Ubertini GraziaMaria
Pedicelli Stefania
Cappa Marco
Cianfarani Stefano
1D.P.U.O. "Bambino Gesù" Children's Hospital, Rome, Italy. 2University of Rome Tor Vergata, Rome, Italy. 3Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden
hrp0092p1-386
Omnitrope® (Recombinant Human Growth Hormone) in Short Children Born Small for Gestational Age (SGA): A Long-Term, Phase IV Study
1Department of Paediatric Endocrinology and Diabetology, Pomeranian Medical University, Szczecin, Poland. 2Sandoz Polska, Warsaw, Poland. 3Hexal AG, Holzkirchen, Germany. 4Sandoz GmbH, Holzkirchen, Germany
hrp0092p1-387
Is there a QTc Interval Prolongation in Girls and Women with Turner Syndrome?
Noordman Iris
Duijnhouwer Anthonie
Coert Misty
Fejzic Zina
Bos Melanie
van der Velden Janiëlle
Kapusta Livia
1Department of Paediatric Endocrinology, Amalia Children's Hospital, Radboud university medical centre, Nijmegen, Netherlands. 2Department of Cardiology, Radboud university medical centre, Nijmegen, Netherlands. 3Department of Paediatrics, Albert Schweitzer Hospital, Dordrecht, Netherlands. 4Department of Paediatric Cardiology, Amalia Children's Hospital, Radboud university medical centre, Nijmegen, Netherlands. 5Paediatric Cardiology Unit, Tel-Aviv Sourasky Medical Centre, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
hrp0092p1-388
Eight Years of Growth Hormone Treatment in a Patient with Schaaf-Yang Syndrome
Erasmus Medical Center, Rotterdam, Netherlands
hrp0092p1-389
Genetic Evaluation of Idiopathic Short Stature
Karaman Birsen
Bas Firdevs
Najafli Adam
Avci Sahin
Kardelen Al Asli Derya
Toksoy Güven
Altunoglu Umut
Poyrazoglu Sükran
Uyguner Zehra Oya
Darendeliler Feyza
Basaran Seher
1Istanbul University, Istanbul Faculty of Medicine, Medical Genetic Department, Istanbul, Turkey. 2Istanbul University, Istanbul Faculty of Medicine, Department of Pediatrics, Pediatric Endocrinology Unit,, Istanbul, Turkey
hrp0092p1-390
Foramen Magnum Stenosis (FMS): Neuroradiological Aspects before and after Cervical Decompression in Paediatric Patients with Achondroplasia (ACH).The 'Achondroplasia Multidisciplinary Gaslini's Group' (AMGG) Istituto Giannina Gaslini, Genova, Italy: Child Neuropsychiatry Unit, Neuroradiology Unit, Department of Paediatrics, Neurosurgery Unit, Orthopedic Unit, Rehabilitation Unit, Pulmonary Disease and Allergy Unit.
Allegri Anna Elsa Maria
Di Iorgi Natascia
Napoli Flavia
Patti Giuseppa
Siri Giulia
Severino Mariasavina
Piatelli Gianluca
Maghnie Mohamad
1Gaslini Children's Hospital, Paediatric Clinic, Genova, Italy. 2Gaslini Children's Hospital, Neuroradiology Unit, Genova, Italy. 3Gaslini Children's Hospital, Neurosurgery Unit, Genova, Italy
hrp0092p1-391
Do Children and Adolescents with Idiopathic short Stature show Postural Alterations? Possible Influence of SHOX Haploinsufficiency in a Pilot Study
Maggio Maria Cristina
Messina Giuseppe
Brusa Jessica
Bellafiore Marianna
Corsello Giovanni
Palma Antonio
1Department Promise "G. D'Alessandro", University of Palermo, Italy, Palermo, Italy. 2Department of Psychology, Educational Science and Human Movement, University of Palermo, Palermo, Italy
hrp0092p1-392
Evaluation of Body Composition and Resting Metabolic Rate in Children with Growth Hormone Deficiency
1Endocrinolody Research Centre, Moscow, Russian Federation. 2Moscow State University, Faculty of Biology,, Moscow, Russian Federation
hrp0092p1-393
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