ORPHA:314911
Severe Canavan disease
Also called Infantile Canavan disease, Neonatal Canavan disease
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:314911 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Global developmental delay
- Motor delay
- Absent speech
- Poor head control
- Inability to walk
- Functional motor deficit