Mayer-Rokitansky-Küster-Hauser syndrome type 2
ORPHA:2578· ICD-10 Q87.8
Definition
A form of Mayer-Rokitansky-Küster-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.
- Prevalence
- 1-9 / 100 000
- Inheritance
- Autosomal dominant, Not applicable
- Age of onset
- Adolescent, Antenatal, Neonatal