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A Japanese family with early-onset ataxia with motor and sensory neuropathy

✍ Scribed by Shunsuke Kobayashi; Hiroshi Takuma; Shigeo Murayama; Masaki Sakurai; Ichiro Kanazawa

Book ID: 119302171
Publisher: Elsevier Science
Year: 2007
Tongue: English
Weight: 894 KB
Volume: 254
Category: Article
ISSN: 0022-510X
DOI: 10.1016/j.jns.2006.12.014

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## Abstract The autosomal dominant (AD) spinocerebellar ataxias (SCAs) and hereditary sensory neuropathies (HSN) are heterogeneous disorders characterized by variable clinical, electrophysiological, and neuropathological profiles. The SCAs are clinically characterized by slowly progressive incoordi