Scientific Programme & Abstracts from the International Meeting in Pediatric Endocrinology (IMPE)

impe0096fc12.1 | GH and IGFs 2 | IMPE2023

Does early treatment with recombinant human growth hormone impact in visual assessment?

Braslavsky Debora , Keselman Ana , Gabriela Ballerini Maria , Cappa Nicolas , Negrete Gabriel , Dech Gaston , Rosenbrock Solange , Ropelato Gabriela , Gamio Susana , Bergadá Ignacio

Background: Current safety of Recombinant human growth hormone (rhGH) treatment arises mainly from postmarketing surveillance. Headache is a relatively frequent symptom in children under rhGH. Secondary intracranial hypertension (SIH), is an adverse effect (AE), usually occurring within the first 12 weeks of treatment associated to headaches. Permanent visual defects are the most feared complication. Scarce information exists regarding incidence and natural hi...

impe0096p94 | Growth and Syndromes | IMPE2023

Potentially pathogenic variants identified by next-generation sequencing in patients with short stature of unknown origin.

Sanguineti Nora , Scaglia Paula , Keselman Ana , Braslavsky Débora , Casali Bárbara , Gabriela Ballerini María , Esnaola Azcoiti María , Armando Romina , Villegas Florencia , del Carmen Fernández María , Correa Lourdes , Martin Ayelen , Ramirez Laura , Landi Estefanía , Izquierdo Agustín , Rosenbrock Solange , Del Rey Graciela , Domené Sabina , Pennisi Patricia , Jasper Hector , Arberas Claudia , Gabriela Ropelato María , Rey Rodolfo , Bergadá Ignacio

Introduction: Short Stature (SS), defined as height below -2 SD, is a common reason for referral to pediatric endocrinologists. Genetic factors determine ~80% of adult height. Lately, next-generation sequencing (NGS) has led to the discovery of an increasing number of novel monogenic causes for SS.Objective: The aim of this work was to identify the genetic etiology of SS of unknown origin (SSUO) in children.<p class=...

impe0096p99 | Growth and Syndromes | IMPE2023

Next generation sequencing implementation for the diagnosis of endocrine disorders: 4 years-experience in a public paediatric hospital

Scaglia Paula , Esnaola Azcoiti María , Izquierdo Agustín , Correa Brito Lourdes , Maier Marianela , Sanso Gabriela , Casali Bárbara , Villegas Florencia , Armando Romina , Sanguineti Nora , Brunello Franco , Rozental Sandra , Raffo Diego , Rosenbrock Solange , Gabriela Ballerini María , Boywitt Adriana , Castro Sebastián , Braslavsky Débora , Freire Analía , Enacan Rosa , Clement Florencia , Grinspon Romina , Keselman Ana , Gryngarten Mirta , Arcari Andrea , Vieites Ana , Chiesa Ana , Papendieck Patricia , del Carmen Fernández María , Martí Marcelo , Arberas Claudia , Bergadá Ignacio , Rey Rodolfo , Gabriela Ropelato María

Introduction: Most paediatric rare diseases have an underlying genetic cause but making a molecular diagnosis is often still a challenge. The incorporation of Next Generation Sequencing (NGS) technologies into research and clinical workflows has improved the diagnosis of these disorders.Objective: To evaluate the process of NGS implementation for the diagnosis of genetic endocrine diseases in a tertiary public paediatric...