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http://20.193.157.4:9595/xmlui/handle/123456789/1696Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Vijaya Patil, Sunilkrishna Muktinaini Rashmi Patil Ashish Verma | - |
| dc.date.accessioned | 2020-01-14T04:51:38Z | - |
| dc.date.available | 2020-01-14T04:51:38Z | - |
| dc.date.issued | 2013-01-27 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/1696 | - |
| dc.description.abstract | Persistent Müllerian duct syndrome is a rare form of internal male pseudohermaphroditism caused by defects in synthesis or action of Müllerian-inhibiting factor, due to which Müllerian duct derivatives, such as uterus, fallopian tube, and upper vagina, are normally present in 46XY males. Here, we report a 26-year-old male with right-sided obstructed inguinal hernia with left undescended testis. On exploration, hernial sac containing bowel loops, uterus with fallopian tubes, upper vagina, and testes were present. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | BLDE(Deemed to be University) | en_US |
| dc.subject | Persistent Müllerian duct syndrome . Transverse testicular ectopia . Hernia uteri inguinale | en_US |
| dc.title | Persistent Mullerian Duct Syndrome: A case report. | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Faculty of General Surgery | |
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