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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