Developmental anomalies of the Mullerian duct are one of the fascinating congenital disorders encountered in which Mayer Rokitansky Kuster Hauser syndrome (MRKH) is one of the wide variety of malformations. The most common presentation in MRKH syndrome is primary amenorrhea with normal development of secondary sexual characteristics and normal female karyotype (46, XX). The ovaries and fallopian tubes are usually functional, but the uterus and upper two-third vagina are either underdeveloped or absent. MRKH syndrome can either be an isolated utero-vaginal aplasia (Type I) or associated with extragenital anomalies (Type II). A case of Type I MRKH syndrome is reported here.
Baby, Anu; Kurian, Simi; and Jose, Rani
"Mayer Rokitansky Kuster Hauser syndrome: A case of Mullerian Agenesis,"
Manipal Journal of Nursing and Health Sciences: Vol. 7
, Article 10.
Available at: https://impressions.manipal.edu/mjnhs/vol7/iss1/10