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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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5558322 | PMC |
| http://dx.doi.org/10.4274/tjod.94809 | DOI Listing |
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