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Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I

✍ Scribed by Dr Sophie Rivaud-Pechoux; Alexandra Dürr; Bertrand Gaymard; Géaraldine Cancel; Christoph J. Ploner; Yves Agid; Alexis Brice; Charles Pierrot-Deseilligny

Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
565 KB
Volume
43
Category
Article
ISSN
0364-5134

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✍ Nathalie Kubis; Alexandra Dürr; Michel Gugenheim; Hervé Chneiweiss; Pilar Mazzet 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 101 KB

Autosomal dominant cerebellar ataxias (ADCAs) are clinically and genetically heterogeneous neurodegenerative disorders. The aim of this study was to evaluate electrophysiologically peripheral nervous system involvement in each of the groups studied and its correlation with the number of CAG repeats.