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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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Библиографические подробности
Главный автор: New, Maria I.
Формат: Artigo
Язык:Inglês
Опубликовано: 1970
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC322683/
https://ncbi.nlm.nih.gov/pubmed/5456802
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