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Selected Publication:

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

 

Leading authors Med Uni Graz
Höllwarth Michael
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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.
Find related publications in this database (using NLM MeSH Indexing)
Child -
Cryptorchidism - surgery
English Abstract - surgery
Fallopian Tubes - abnormalities
Female - abnormalities
Humans - abnormalities
Karyotyping - abnormalities
Male - abnormalities
Pseudohermaphroditism - genetics
Testis - surgery
Uterus - abnormalities

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