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Spinocerebellar ataxia 43

rare

Spinocerebellar ataxia type 43 is a rare autosomal dominant cerebellar ataxia type I disorder characterized by late adult-onset of slowly progressive cerebellar ataxia, typically presenting with balance and gait disturbances, in association with axonal peripheral neuropathy resulting in reduced/absent deep tendon reflexes and sensory impairment. Lower limb pain and amyotrophy may be present, as well as various cerebellar signs, including dysarthria, nystagmus, hypometric saccades and tremor.

Causal genes
MME
Also known as
autosomal dominant cerebellar ataxia caused by mutation in MME · MME autosomal dominant cerebellar ataxia · SCA43 · spinocerebellar ataxia 43; SCA43 · spinocerebellar ataxia type 43

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