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Published on: May 10, 2022
Mayer-Rokitansky-Kuster-Hauser syndrome associated with rectovestibular fistula
Charu Tiwari1, Hemanshi Shah1, Mukta Waghmare1
1Topiwala National Medical College & Bai Yamunabai Laxman Nair Hospital, Mumbai, India.
Abstract:
A female neonate with two openings in the introitus and an absent anal opening at the anal site presents a diagnostic challenge. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome associated with rectovestibular fistula, though rare, should be kept in mind as a differential diagnosis of this presentation. We present such a case in a one-year-old female child with MRKH syndrome and rectovestibular fistula.
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