Ovarian Cancer and Mayer–Rokitansky–Küster–Hauser (MRKH) Syndrome a Rare Combination

Background Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome is a rare syndrome affecting one out of 4500 women. It is characterized by utero-vaginal aplasia with normal development of secondary sexual characteristics and normal 46, XX karyotype.