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JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2007; 17 (1): 57-58
in English | IMEMR | ID: emr-83232

ABSTRACT

Mayer Rokitansky Kuster Hauser [MRKH] syndrome is a rare disorder, characterized by the congenital absence of uterus and associated renal tract anomalies. The case presented with primary amenorrhea and primary infertility, despite development of normal female secondary sexual characteristics. CT scan revealed absent uterus, a solitary left sided pelvic kidney and a vesicovaginal communication that, on cystoscopy, revealed urogenital sinus anomaly manifesting as a common channel formed due to absent anterior wall of vagina and posterior wall of urethra. The urogenital sinus anomaly in MRKH syndrome has not been reported earlier


Subject(s)
Humans , Female , Mullerian Ducts/abnormalities , Abnormalities, Multiple/diagnostic imaging , Syndrome , Vesicovaginal Fistula/etiology , Vesicovaginal Fistula/diagnostic imaging , Tomography, X-Ray Computed
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