Mayer-Rokitansky-Küster-Hauser syndrome type 2

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome type 2, a form of MRKH syndrome, is characterized by congenital aplasia of the uterus and upper 2/3 of the vagina that is associated with at least one other malformation such as renal, vertebral, or, less commonly, auditory and cardiac defects. The acronym MURCS (MCllerian duct aplasia, Renal dysplasia, Cervical Somite anomalies) is also used.

Also known as: MRKH syndrome type 2, MURCS association, Mayer-Rokitansky-Küster-Hauser syndrome type 2, Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome, atypical MRKH syndrome, Klippel-Feil deformity, conductive deafness, and absent vagina, MRKH, type 2, MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies

3 clinical trials for this condition and its sub-types.