TITLE

Sporadic Creutzfeldt—Jakob disease with cerebellar ataxia at onset in the UK

AUTHOR(S)
Cooper, S. A.; Murray, K. L.; Heath, C. A.; Will, R. G.; Knight, R. S. G.
PUB. DATE
November 2006
SOURCE
Journal of Neurology, Neurosurgery & Psychiatry;Nov2006, Vol. 77 Issue 11, p1273
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Objective: To determine the frequency, in the UK, of sporadic Creutzfeldt-Jakob Disease (sCJD) with a cerebellar ataxic onset, and to describe the clinical features of the syndrome. Methods: A retrospective review of autopsy-proved cases of sCJD cases in the UK, 1990–2005, identifying those presenting with cerebellar features without early cognitive decline. Results: 29 of 618 (5%) patients with sCJD had an isolated cerebellar onset. Mean illness duration was 9 months. Subsequently, 21 (72%) developed myoclonus and 23 (79%) developed pyramidal features. Magnetic resonance imaging showed high signal in the basal ganglia in 11 of 14 (79%) patients. 7 of 15 (47%) patients were valine homozygotic at prion protein gene (PRNP)-129. Only 8 (28%) cases were referred to the surveillance unit after death. Conclusion: A better definition of sCJD presenting with an isolated cerebellar syndrome might improve future case recognition and contribute to the determination of its cause.
ACCESSION #
23093972

 

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