Adult-onset autosomal dominant leukodystrophy
ORPHA:99027· ICD-10 E75.2
Definition
A rare, slowly progressive neurological disorder involving central nervous system demyelination, leading to autonomic dysfunction, ataxia and mild cognitive impairment.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal dominant
- Age of onset
- Adult