Sensorimotor neuropathy with ataxia, autosomal dominant (medical condition)
A rare genetic disorder (chromosome 7q22-31 defect) characterized by muscle atrophy and sensory loss. The severity of symptoms is variable. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types. See also Spinocerebellar ataxia 18
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