1. Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings.
- Author
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Torrens, L., Burns, E., Stone, J., Graham, C., Wright, H., Summers, D., Sellar, R., Porteous, M., Warner, J., and Zeman, A.
- Subjects
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NEUROPSYCHOLOGY , *FRIEDREICH'S ataxia , *NEUROPSYCHOLOGICAL tests , *ATAXIA , *MAGNETIC resonance imaging , *PATIENTS - Abstract
Objectives – The objectives of this study were to: (i) establish whether the spinocerebellar ataxia type 8 (SCA 8) expansion is associated with ataxia in Scotland; (ii) test the hypothesis that SCA 8 is associated with neuropsychological impairment; and (iii) review neuroradiological findings in SCA 8. Methods – The methods included: (i) measurement of SCA 8 expansion frequencies in ataxic patients and healthy controls; (ii) comprehensive neuropsychological assessment of patients with SCA 8 and matched controls, neuropsychiatric interview; and (iii) comparison of patient and matched control magnetic resonance imaging (MRI) scans. Results – (i) 10/694 (1.4%) unrelated individuals with ataxia had combined CTA/CTG repeat expansions >100 compared to 1/1190 (0.08%) healthy controls ( P < 0.0005); (ii) neuropsychological assessment revealed a dysexecutive syndrome among SCA 8 patients, not readily explained by motor or mood disturbance; neuropsychiatric symptoms occurred commonly; (iii) cerebellar atrophy was the only salient MRI abnormality in the patient group. Conclusions – The SCA 8 expansion is associated with ataxia in Scotland. The disorder is associated with a dysexecutive syndrome. [ABSTRACT FROM AUTHOR]
- Published
- 2008
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