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.

Rectovaginal fistula

Mayer-Rokitansky-Kuster-Hauser syndrome

© 2025 The Authors. Published by Elsevier Inc.