Höllwarth, M.
Persistence of the oviduct (pseudohermaphroditismus masculinus internus)
Zentralbl Chir. 1979; 104(4): 218-223.
(- Case Report)
Web of SciencePubMed
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.
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