Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1149
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dc.contributor.authorSavitri Mallikarjun Nerune, Surekha B Hippargi Namrata B Mestri Nikhil M Mehrotra-
dc.date.accessioned2019-11-06T10:58:13Z-
dc.date.available2019-11-06T10:58:13Z-
dc.date.issued2016-
dc.identifier.issn2249782X-
dc.identifier.urihttp://hdl.handle.net/123456789/1149-
dc.description.abstractPersistent Mullerian Duct Syndrome (PMDS) is a rare form of internal male pseudohermaphroditism, characterised by presence of Mullerian duct derivatives in a genotypic and phenotypic male. It is caused by absence of anti- Mullerian hormone or defective functioning of its receptors. We report a case of 19-year-old cryptorchid male with history of orchideopexy who was clinically and radiologically diagnosed as left sided chylocele. A definitive diagnosis of PMDS with ovarian endometriosis was made on histopathological examination which is important for genetic counselling and to reduce complications like infertility and neoplastic transformation. We report this case of PMDS with ovary showing evidence of endometriosis for its rarity.en_US
dc.language.isoenen_US
dc.publisherBLDE(Deemed to be University)en_US
dc.subjectAnti-Mullerian hormone, Male pseudohermaphrodite, Orchideopexyen_US
dc.title"Persistent mullerian duct syndrome with ovarian endometriosis- a rare case report."en_US
dc.typeArticleen_US
Appears in Collections:Faculty of Pathology

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