Mayer- Rokitansky-Kuster-Hauser (MRKH) syndrome is a variation in the prenatal development of the female genital tract. Girls and women with MRKH have an absent or short vagina and absent or incompletely developed uterus, but typically functioning ovaries. There may be associated renal or skeletal differences. Synonyms: Mullerian agenesis
Genetic Information from: NIH, National Library of Medicine, Genetics Home Reference https://ghr.nlm.nih.gov/condition
https://ghr.nlm.nih.gov/condition/mayer-rokitansky-kuster-hauser-syndrome
- Mayer-Rokitansky-Küster-Hauser-Biason-Lauber syndrome, see Müllerian aplasia and hyperandrogenism
- Mayer-Rokitansky-Küster-Hauser-like syndrome, see Müllerian aplasia and hyperandrogenism