ORPHA:363722
Alexander disease type II
Also called AxD type II
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:363722 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Cervical spinal cord atrophy
- Abnormality of the medulla oblongata
- Nystagmus
- Ataxia
- Spasticity
- Dysarthria