Author:
Major Toby,Tiet May Yung,Horvath Rita,Hensiek Anke E.
Abstract
AbstractAtaxia-Telangiectasia
(A-T) is an autosomal recessive neurodegenerative disease associated with cerebellar ataxia and extrapyramidal features. A-T has a complex and diverse phenotype with varying rates of disease progression. The development of robust natural history studies and therapeutic trials relies on the accurate recording of phenotype using relevant and validated severity of illness indexes. We compared the commonly used Scale for the Assessment and Rating of Ataxia (SARA) and the disease-specific A-T Neurological Examination Scale Toolkit (A-T NEST), in our adult A-T cohort. We found a strong correlation between A-T NEST and the established SARA score, validating the use of A-T NEST and SARA in capturing the natural history of A-T patients.
Funder
Addenbrooke's Charitable Trust, Cambridge University Hospitals
Action for A-T, BrAshAT and the A-T Society
Wellcome Trust
Medical Research Council
European Research Council
Newton Fund
International Centre for Genomic Medicine in Neuromuscular Diseases
NIHR Cambridge Biomedical Research Centre
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Cited by
1 articles.
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