SUN-250 Natural History of Growth in Patients with SHOX Gene Haploinsufficiency and Impact of Treatment with rhGH in Adult Height

Introduction: The SHOX gene haploinsufficiency is the main monogenic cause of short stature, being observed in 56% to 100% of patients with Leri-Weill dyschondrosthosis (LWD) and in 1% to 14% of children with idiopathic short stature (ISS). The diagnosis allows the establishment of a suitable progno...

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Bibliografische gegevens
Gepubliceerd in:J Endocr Soc
Hoofdauteurs: Menezes De Andrade, Nathalia, Vasques, Gabriela, Funari, Mariana, Nishi, Mirian, Scalco, Renata, Malaquias, Alexsandra, Mendonca, Berenice, Jorge, Alexander
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Endocrine Society 2019
Onderwerpen:
Pediatric Endocrinology
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6553356/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-250
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