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Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study

✍ Scribed by Velázquez-Pérez, Luis; Rodríguez-Labrada, Roberto; Canales-Ochoa, Nalia; Montero, Jacqueline Medrano; Sánchez-Cruz, Gilberto; Aguilera-Rodríguez, Raúl; Almaguer-Mederos, Luis E; Laffita-Mesa, José M

Book ID
122256385
Publisher
The Lancet
Year
2014
Tongue
English
Weight
444 KB
Volume
13
Category
Article
ISSN
1474-4465

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✍ Sascha Hering; Clemens Achmüller; Andrea Köhler; Werner Poewe; Raine Schneider; 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 457 KB

## 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