Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6

@article{Linnemann2015PeripheralNI,
  title={Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6},
  author={Christoph Linnemann and Sophie T{\'e}zenas du Montcel and Maryla Rakowicz and Tanja Schmitz-H{\"u}bsch and Sandra Szymanski and Jos{\'e} Berciano and Bart van de Warrenburg and Karine Pedersen and Chantal Depondt and Rafal Rola and Thomas Klockgether and Antonio Garc{\'i}a and Gurkan Mutlu and Ludger Sch{\"o}ls},
  journal={The Cerebellum},
  year={2015},
  volume={15},
  pages={165-173}
}
Spinocerebellar ataxias (SCAs) are characterized by autosomal dominantly inherited progressive ataxia but are clinically heterogeneous due to variable involvement of non-cerebellar parts of the nervous system. Non-cerebellar symptoms contribute significantly to the burden of SCAs, may guide the clinician to the underlying genetic subtype, and might be useful markers to monitor disease. Peripheral neuropathy is frequently observed in SCA, but subtype-specific features and subclinical… CONTINUE READING
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