Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
ORPHA:1014· ICD-10 Q87.8
Definition
A rare multiple congenital anomalies syndrome characterized by association of congenital total alopecia, mild intellectual deficit and hypergonadotropic hypogonadism.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Unknown
- Age of onset
- Neonatal