Persistent Mullerian Duct Syndrome: A case report.

Vijaya Patil, Sunilkrishna Muktinaini  Rashmi Patil Ashish Verma

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