Spinocerebellar ataxia, autosomal recessive 4: A rare neurological disorder caused by a genetic defect (chromosome 1p36, recessive) and resulting in ataxia and eye movement problems. More detailed information about the symptoms, causes, and treatments of Spinocerebellar ataxia, autosomal recessive 4 is available below.
See full list of 9 symptoms of Spinocerebellar ataxia, autosomal recessive 4
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