Mayer-Rokitansky-Kuster-Hauser syndrome type 2

info · Syndrome

A Mayer-Rokitansky-Kuster-Hauser syndrome characterized by congenital aplasia of the uterus and upper two thirds of the vagina that is associated with at least one other malformation such as renal, vertebral, or, less commonly, auditory and cardiac defects.

Signs and symptoms

Cleft palate
Hypoplasia of the uterus
Abnormal rib morphology
Short stature
Unilateral renal agenesis
Ectopic kidney
Cerebellar cyst
Abnormality of the vertebral column
Bicornuate uterus
Sprengel anomaly

Also known as: MRKH syndrome type 2; MURCS; MURCS association; atypical MRKH syndrome; mullerian duct aplasia, unilateral renal aplasia, and cervicothoracic somite dysplasia