Please use this identifier to cite or link to this item:
http://20.193.157.4:9595/xmlui/handle/123456789/1696| Title: | Persistent Mullerian Duct Syndrome: A case report. |
| Authors: | Vijaya Patil, Sunilkrishna Muktinaini Rashmi Patil Ashish Verma |
| Keywords: | Persistent Müllerian duct syndrome . Transverse testicular ectopia . Hernia uteri inguinale |
| Issue Date: | 27-Jan-2013 |
| Publisher: | BLDE(Deemed to be University) |
| 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. |
| URI: | http://hdl.handle.net/123456789/1696 |
| Appears in Collections: | Faculty of General Surgery |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.