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Alternative Terrebonne portable massage table symbols. For a discussion of genetic heterogeneity of spastic ataxia, see SPAX1 Autosomal recessive spastic ataxia of Charlevoix-Saguenay is a complex neurodegenerative disorder usually characterized by early childhood onset of cerebellar ataxia, pyramidal tract s, and peripheral neuropathy. Most patients become wheelchair-bound; cognitive function is usually not affected. Some patients may have atypical features, such as later onset or initial presentation of peripheral neuropathy summary by Baets et al.

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