Spinocerebellar ataxias (SCAs) are a group of neurodegenerative diseases with ataxia as the main clinical manifestation. The phenotypes, gene mutations, and involved sites of different subtypes show a high degree of heterogeneity. The incidence of SCA varies greatly among different subtypes and the case of SCA40 is extremely rare. The aim of this study is to report a rare case of SCA40 and systematically review the incidence, gene mutation, and phenotype of SCAs, especially SCA40.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525662 | PMC |
http://dx.doi.org/10.1515/tnsci-2020-0190 | DOI Listing |
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