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Intellectual disability-hyperkinetic movement-truncal ataxia syndrome

ORPHA:369847· ICD-10 G25.5

Definition

A rare, genetic, syndromic intellectual disability disease characterized by global developmental delay, microcephaly, mild to moderate intellectual disability, truncal ataxia, trunk and limb, or generalized, choreiform movements, and elevated serum creatine kinase levels. Variably associated features include mild cerebral atrophy, muscular weakness or hypotonia in early childhood, and/or seizures. Ocular abnormalities (e.g. exophoria, anisometropia, amblyopia) have been reported.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal recessive
Age of onset
Childhood