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Charlevoix-Saguenay Spastic Ataxia
An autosomal recessive cerebellar ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy, is caused by homozygous or compound heterozygous mutation in the gene e
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When to seek help
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Overview
An autosomal recessive cerebellar ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy, is caused by homozygous or compound heterozygous mutation in the gene e
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.