SUN-725 Clinical and Genetic Features of Families with Maternally Inherited Central Precocious Puberty

Context: The clinical recognition of familial central precocious puberty (CPP) has significantly increased in the last years. This fact can be related to the recent descriptions of genetic causes associated with this pediatric condition, such as loss-of-function mutations of two imprinted genes (MKR...

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Détails bibliographiques
Publié dans:J Endocr Soc
Auteurs principaux: Tinano, Flávia Rezende, Canton, Ana Pinheiro Machado, Montenegro, Luciana Ribeiro, Leal, Andrea de Castro, Ramos, Carolina, Piovesan, Maiara Ribeiro, Seraphim, Carlos Eduardo, de Faria, Aline Guimarães, Mendonca, Berenice Bilharinho, Brito, Vinicius Nahime, Latronico, Ana Claudia
Format: Artigo
Langue:Inglês
Publié: Oxford University Press 2020
Sujets:
Genetics and Development (including Gene Regulation)
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207300/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1315
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