Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency
ORPHA:404493· ICD-10 G11.1
Definition
A rare hereditary ataxia characterized by an early onset symptomatic generalized epilepsy, progressive cerebellar ataxia resulting in significant difficulties to walk or wheelchair dependency, and intellectual disability.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal recessive
- Age of onset
- Childhood, Infancy