Creutzfeldt-Jakob disease other diagnostic studies: Difference between revisions
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Revision as of 14:52, 27 December 2012
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Creutzfeldt-Jakob disease Microchapters |
Differentiating Creutzfeldt-Jakob disease from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Other Diagnostic Studies
Electroencephalography
Characteristic triphasic spikes
Biopsy
In one third of patients with sporadic CJD, deposits of prion protein (scrapie), PrPSc, can be found in the skeletal muscle and/or the spleen. Diagnosis of vCJD can be supported by biopsy of the tonsils, which harbour significant amounts of PrpSc; however, biopsy of brain tissue is the definitive diagnostic test.