Abstract
A spectrum of Müllerian malformations known as the Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects females with normal endocrine function and is characterized by congenital vaginal aplasia and an absence of the uterus or a rudimentary one. The ovaries and fallopian tubes are present. Primary amenorrhea in females with normally developed secondary sexual characteristics and normal external genitalia is the main symptom. There are 2 distinct kinds of this condition. It could exist alone (type I) or alongside other abnormalities (type II).
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