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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Front Endocrinol (Lausanne)
मुख्य लेखकों: Papadakis, Georgios, Kandaraki, Eleni A., Tseniklidi, Ermioni, Papalou, Olga, Diamanti-Kandarakis, Evanthia
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Frontiers Media S.A. 2019
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC6593353/
https://ncbi.nlm.nih.gov/pubmed/31275245
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2019.00388
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