Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review

Background: Twenty-one-hydroxylase–deficient non-classic adrenal hyperplasia (NC-CAH) is a very common autosomal recessive syndrome with prevalence between 1:1,000 and 1:2,000 individuals and the frequency varies according to ethnicity. On the other hand, polycystic ovary syndrome has a familial bas...

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Detalles Bibliográficos
Autores principales: Papadakis, Georgios, Kandaraki, Eleni A., Tseniklidi, Ermioni, Papalou, Olga, Diamanti-Kandarakis, Evanthia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593353/
https://www.ncbi.nlm.nih.gov/pubmed/31275245
http://dx.doi.org/10.3389/fendo.2019.00388

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593353/
https://www.ncbi.nlm.nih.gov/pubmed/31275245
http://dx.doi.org/10.3389/fendo.2019.00388

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