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[Persistence of the oviduct (pseudohermaphroditismus masculinus internus)]
Zentralblatt Fur Chirurgie
|January 1, 1979
Abstract:
Internal male pseudohermaphroditism is a rare malformation. Its reason is the lack of the Müllerian inhibiting substance produced by the fetal Sertoli cells. Therefore, additional female genital organs exist in a normal male. Genetic determination seems to be possible. Early correction of cryptorch testes is the therapy of choice and promises fertility for some patients.