| Literature DB >> 28913139 |
Charu Tiwari1, Hemanshi Shah1, Mukta Waghmare1, Kiran Khedkar1.
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.Entities:
Keywords: Mayer-Rokitansky-Kuster-Hauser syndrome; atypical; rectovestibular fistula
Year: 2017 PMID: 28913139 PMCID: PMC5558322 DOI: 10.4274/tjod.94809
Source DB: PubMed Journal: Turk J Obstet Gynecol ISSN: 2149-9330