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Sudden cardiac death in a case of spinocerebellar ataxia (Friedreich-like phenotype)

✍ Scribed by V. Fineschi; F. Panarese; P. Zeppa; I. Riezzo; P. Ricci; M.T. Dotti; A. Federico

Book ID
116543834
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
145 KB
Volume
106
Category
Article
ISSN
0167-5273

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## Abstract We report a 67 years old female patient out of a multigenerational family with spinocerebellar ataxia type 2 (SCA2) with an unusually benign course of disease. Although all SCA2 gene carriers have by now developed the predominant gait ataxia and brainstem oculomotor dysfunction, the ind