ORPHA:314918
Mild Canavan disease
Also called Juvenile Canavan disease
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Europe)
- Rarity class
- <1 / 1 000 000
ORPHA:314918 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Motor delay
- Specific learning disability
- Poor speech
- Mild global developmental delay
- Abnormal enzyme/coenzyme activity
- Macrocephaly