[Clinical peculiarities in a female patient with the Mayer-Rokitansky-Küster-Hauser syndrome].

Described is a case with the Mayer-Rokitansky-Küster-Hauser syndrome with normal pubescent female development, moderate hair virilismus, double rudimentary uterus, incomplete development of the vagina, ovarian dystrophy and abnormalities in the sex chromatin and the gonosomal complement. Discussion on the clinical variety and the ethiopathogenesis of the disease is performed.