TIME COURSE OF CENTRAL PRECOCIOUS PUBERTY DEVELOPMENT CAUSED BY AN MKRN3 GENE MUTATION: A PRISMATIC CASE

BACKGROUND: Loss-of-function mutations in the imprinted gene MKRN3 represent the most common known genetic defects associated with central precocious puberty (CPP). METHODS: We report the first case of a girl carrying an MKRN3 mutation detected in childhood and followed until the development of pube...

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Detalhes bibliográficos
Publicado no:Horm Res Paediatr
Main Authors: Stecchini, Monica F., Macedo, Delanie B., Reis, Ana Claudia S., Abreu, Ana Paula, Moreira, Ayrton C., Castro, Margaret, Kaiser, Ursula B., Latronico, Ana Claudia, Antonini, Sonir R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5061599/
https://ncbi.nlm.nih.gov/pubmed/27424312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000447515
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