The paired Mullerian or paramesonephric ducts fuse between 6 and 11 weeks of gestation to form uterus, cervix and upper two-thirds of vagina. Mullerian duct anomalies (MDA) result from disruption in any of the three stages of uterine development, i.e. organogenesis, fusion or septal resorption. 1 Ovaries develop from primordial germ cells, while lower one-third of vagina develops from sinovaginal bulb. Owing to the different embryological origins, ovaries and lower third of vagina are not involved in MDA. 2 The prevalence of MDA is reported to be 1-5%. 2 American Fertility Society (AFS), has classified MDA into seven basic types, from Type I to Type VII. 3 Out of these seven types, Type I MDA also called as Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, which reportedly accounts for nearly 15% of total case load. 2 MRKH syndrome is characterized by complete/partial agenesis of uterus and upper two-thirds of vagina, with normal bilateral ovaries,