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Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

ORPHA:504476· ICD-10 G11.2

Definition

A rare slowly progressive autosomal recessive syndromic cerebellar ataxia characterized by late-onset cerebellar dysfunction (including gait and limb ataxia, nystagmus, and dysarthria), bilateral vestibulopathy (abnormal vestibulo-ocular reflex), and axonal sensory neuropathy. Variable features may include chronic cough and autonomic dysfunction. Brain imaging usually shows cerebellar atrophy.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal recessive
Age of onset
Adult, Elderly