Male pseudohermaphroditism with gynaecomastia due to testicular 17-ketosteroid reductase deficiency.

@article{Akesode1977MalePW,
  title={Male pseudohermaphroditism with gynaecomastia due to testicular 17-ketosteroid reductase deficiency.},
  author={F Ademola Akesode and Walter J. Meyer and Claude J. Migeon},
  journal={Clinical endocrinology},
  year={1977},
  volume={7 6},
  pages={443-52}
}
A 28-year-old male pseudohermaphrodite with gynaecomastia was raised as a female until the age of 17 years, at which time he developed masculine features (deepening of the voice, development of facial hair, male distribution of body hair and male body habitus) and assumed a male gender role. He had a small phallus with perineal urethra, absence of labioscrotal fusion, presence of vaginal pouch and undescended testes. The testicular biopsy showed hyalinization of the tubular basement membrane… CONTINUE READING
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