Puvvada Sandeep, S. Shanthakumar, Venkata Mahesh Chalumuru, D. Ramesh, Tarun Dilip Javali
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Rectovaginal fistula in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome
MRKH syndrome is defined by the congenital absence of the uterus and the upper two-thirds of the vagina in females, who otherwise exhibit normal secondary sexual characteristics and possess a typical 46, XX karyotype. Here we report a case of 23 year old female diagnosed with Mayer-Rokitansky-Kuster-Hauser syndrome when presenting with features of rectovaginal fistula.
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