ORPHA:363717
Alexander disease type I
Also called AxD type I
- Body system
- Neurological diseases
- Inheritance pattern
- Not applicable
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:363717 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Abnormal cerebral white matter morphology
- Focal T2 hyperintense basal ganglia lesion
- Seizure
- Cerebellar atrophy
- Failure to thrive
- Scoliosis