Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
ORPHA:314404· ICD-10 G11.2
Definition
A rare polymorphic disorder, subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1), characterized by ataxia, sensorineural deafness and narcolepsy with cataplexy and dementia.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant, Not applicable
- Age of onset
- Adult