00596nz a2200217n 4500 230628|||anznnbab||||||||||||||a|||||||d homoit0002865 https://homosaurus.org/v3/homoit0002865 homoit Mayer-Rokitansky-Küster-Hauser syndrome MRKH syndrome Müllerian agenesis Müllerian duct anomalies Müllerian duct variations Intersex variations https://homosaurus.org/v3/homoit0000669 Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome occurs when a person's Müllerian ducts, which typically become the uterus and upper portion of the vagina during fetal development, do not develop in the typical way. People with MRKH have XX chromosomes and are usually born with a vulva and either a vagina that is shorter than typical or no vagina. They usually do not have a cervix and may have a partial uterus (uterine remnant) or no uterus. They often do not mensturate but may experience cyclic pain if they have a uterine remnant with endometrial lining, and they can develop menstruation-related conditions like endometriosis.