Female pseudohermaphroditism caused by caudal dysgenesis.

P Wieacker, U Grumpelt, T Schulz,B Gharavi,S Avenarius,S Jakubiczka, M Stumm

CYTOGENETICS AND CELL GENETICS（2001）

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摘要

We report on two cases of female pseuduhermaphroditism associated with anorectal, Mullerian duct, and urinary tract malformations. We suggest that this form of female pseudohermaphroditism is an extreme manifestation of the caudal type of VATER association. Copyright (C) 2001 S. Karger AG, Basel.

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urinary tract

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