Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
ORPHA:2229· ICD-10 I42.0
Definition
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH).
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal recessive
- Age of onset
- Infancy, Neonatal