X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome
ORPHA:1568· ICD-10 Q04.8
Definition
A rare central nervous system malformation characterized by severe intellectual deficit, early hypotonia with progression to spasticity and contractures, choreoathetosis, seizures, dysmorphic face (long face with prominent forehead), and brain imaging abnormalities such as Dandy-Walker malformation, and iron deposition.
- Prevalence
- <1 / 1 000 000
- Inheritance
- X-linked recessive
- Age of onset
- Antenatal, Neonatal