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Male pseudohermaphroditism due to 17α-hydroxylase deficiency

This is the first report of a male with 17α-hydroxylase deficiency resulting in male pseudohermaphroditism, ambiguous external genitalia, absence of male secondary sexual characteristics, and gynecomastia at puberty. Diagnosis was based on extensive studies of steroid metabolism including the follow...

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Detalles Bibliográficos
Autor Principal: New, Maria I.
Formato: Artigo
Idioma:Inglês
Publicado: 1970
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC322683/
https://ncbi.nlm.nih.gov/pubmed/5456802
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