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2.  Colovaginoplasty in a Case of Mayer-Rokitansky-Kuster-Hauser Syndrome 
Mayer-Rokitansky-Kuster-Hauser Syndrome (MRKHS) is characterized by various abnormalities of paramesonephric duct structures; vaginal aplasia being the commonest anomaly in the spectrum. We report a 17-year-old girl; a case of MRKHS with vaginal agenesis. The cervix was present but atretic; uterus, fallopian tubes and ovaries were normal. There were no associated renal or skeletal defects. Colovaginoplasty was done to bridge the gap between uterus and introitus. Postoperatively, small part of colovaginoplasty flap became necrotic posteriorly, which was ultimately managed by insetting of labial flap.
PMCID: PMC4005094  PMID: 24834388
Mayer-Rokitansky-Kuster-Hauser Syndrome; Vaginal agenesis; Colovaginoplasty
3.  True Hermaphrodite: A Case Report 
True hermaphrodite is one of the rarest variety of disorders of sexual differentiation (DSD) and represents only 5% cases of all. A 3-year-old child presented with left sided undescended testis and penoscrotal hypospadias. Chordee correction was performed 18 months back, elsewhere. At laparotomy Mullerian structures were present on left side. On right side testis was normally descended into the scrotum.
PMCID: PMC3418019  PMID: 22953283
True hermaphrodite;  Persistent mullerian duct syndrome;  Disorders of sexual differentiation

Results 1-3 (3)