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Eye movement abnormalities in spinocerebellar ataxia type 17

J. Hübner, A. Sprenger, J. Hagenah, C. Klein, H. Rambold, C. Zühlke, D. Kömpf, A. Rolfs, H. Kimmig, C. Helmchen · Aktuelle Neurologie · 2006 · Heft 09

Dokument
1103570
CareLit-ID
Jahr
2006
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Aktuelle Neurologie
Autor:innen
J. Hübner, A. Sprenger, J. Hagenah, C. Klein, H. Rambold, C. Zühlke, D. Kömpf, A. Rolfs, H. Kimmig, C. Helmchen
Ausgabe
Heft 09 / 2006
Seiten
–
Erschienen: 2006-09-27 00:00:00
ISSN
0302-4350
DOI
10.1055/s-2006-953057

Zusammenfassung

Aims: Spinocerebellar ataxia type 17 (SCA17) is associated with an expansion of CAG/CAA trinucleotide repeats in the gene encoding TATA-binding protein (TBP). The aim of this study was to characterize eye movements in SCA17 and to localize oculomotor deficits. Methods: Eye movements of 13 SCA17 mutation carriers and 13 age-matched control subjects were recorded using the video-based EYELINK II system and compared using ANOVA (p

Schlagworte

Eye Movements Ataxia Acceleration Alleles ANOVA Movement Aktuelle Neurologie