OR18-2 Clinical, Hormonal and Genetic Characterization of Familial Central Precocious Puberty

 : Context: Familial central precocious puberty (CPP) is a prevalent form (about 27.5%) of precocious puberty. Loss-of-function mutations in two maternally imprinted genes, MKRN3 and DLK1, were identified in families with CPP showing dominant autosomal inheritance with paternal transmission. Materna...

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Detalles Bibliográficos
Autores principales: Argente, Jesús, Brito, Vinicius, Guimaraes, Aline, Latronico, Ana Claudia, Leal, Andrea, Mendonça, Berenice, Montenegro, Luciana, Piovesan, Maiara, Ramos, Carolina, Seraphim, Carlos, Tinano, Flavia, Canton, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625673/
http://dx.doi.org/10.1210/jendso/bvac150.1279

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625673/
http://dx.doi.org/10.1210/jendso/bvac150.1279

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