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17 alpha-Hydroxylase deficiency with persistence of müllerian ducts in a genotypic male and paradoxical aldosterone secretion.

We report a case of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency in a Chinese genotypic male patient. Despite the male genotype, normal female external genitalia were present and with the introduction of cyclical oestrogen therapy withdrawal bleeding occurred, confirming the...

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Detalhes bibliográficos
Main Authors: Panesar, N. S., Yeung, V. T., Chan, J. C., Shek, C. C., Nicholls, M. G., Cockram, C. S.
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 1993
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2399616/
https://ncbi.nlm.nih.gov/pubmed/8506204
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