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Rev Neurol (Paris). 2000 Jul;156(6-7):616-21.

[Non-familial Creutzfeldt-Jakob disease: a study of 53 cases].

[Article in French]

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1
Service de Neurologie D, Hôpital Neurologique Pierre Wertheimer, Lyon. glap@wanadoo.fr

Abstract

Creutzfeldt-Jakob disease (CJD) is the most frequent human spongiform encephalopathy. We have analyzed 53 cases of definite non familial CJD over a study period of 28 years. All were autopsied in the same neuropathological unit. Clinical and epidemiological data were in accordance with previous studies: low incidence of CJD under the age of 40, high incidence around the sixty years of age (26%) a sex ratio at 0.65 and high frequency of myoclonus, dementia and cerebellar ataxia during evolution (78%). This study highlights the rapidity at the onset of the disease (within 24 hours) in 16% of the cases. EEG disclosed typical pseudoperiodic activity in only 53% of cases and cerebral MRI showed high T2 signal intensity in basal nuclei in 15%. This regional study is the second of its nature to be carried out in France, the first one covering the area of Paris.

PMID:
10891795
[Indexed for MEDLINE]
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