Spinocerebellar ataxia, autosomal recessive 1: A neurological disorder characterized by progressive ataxia, tremor and muscle weakness and wasting. The rate of progression and severity is variable with some needing wheelchairs in their second decade and others still capable of some walking in their 4th decade. More detailed information about the symptoms, causes, and treatments of Spinocerebellar ataxia, autosomal recessive 1 is available below.
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Prognosis for Spinocerebellar ataxia, autosomal recessive 1: wheelchair dependency occurs eventually
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