Genotyping of congenital adrenal hyperplasia due to 21-hydroxylase deficiency presenting as male infertility: Case report and literature review

We describe here two infertile male patients who were referred to our hospital with azoospermia at the ages of 33 and 30 years, respectively. Hormonal examinations led to a diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency in both patients. Genotyping revealed that t...

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Detalhes bibliográficos
Main Authors: Sugino, Y., Usui, T., Okubo, K., Nagahama, K., Takahashi, T., Okuno, H., Hatayama, H., Ogawa, O., Shimatsu, A., Nishiyama, H.
Formato: Artigo
Idioma:Inglês
Publicado em: Kluwer Academic Publishers-Plenum Publishers 2006
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3455103/
https://ncbi.nlm.nih.gov/pubmed/17033937
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-006-9062-0
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