Abstract
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome represents a spectrum of congenital anomalies affecting the Mullerian ductal system ranging from complete agenesis of the upper 2/3 of the vagina, cervix and uterus to isolated cervical agenesis. Pelvic pain and renal anomalies can be associated with MRKH. Our objective was to use the classification system provided by Buttram et al. to describe prevalence of MRKH subtypes and associations with pelvic pain and renal anomalies.
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