Creutzfeldt-Jakob disease laboratory findings: Difference between revisions
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==Laboratory Findings== | ==Laboratory Findings== | ||
The diagnosis of CJD is suspected when there are typical clinical symptoms and signs such as rapidly progressing dementia with [[myoclonus]]. | The diagnosis of CJD is suspected when there are typical clinical symptoms and signs such as rapidly progressing dementia with [[myoclonus]]. Analysis of CSF for [[14-3-3 protein]] is done to establish diagnosis. | ||
==References== | ==References== | ||
Revision as of 16:34, 26 December 2012
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Creutzfeldt-Jakob disease Microchapters |
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Differentiating Creutzfeldt-Jakob disease from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Laboratory Findings
The diagnosis of CJD is suspected when there are typical clinical symptoms and signs such as rapidly progressing dementia with myoclonus. Analysis of CSF for 14-3-3 protein is done to establish diagnosis.