Creutzfeldt-Jakob disease laboratory findings: Difference between revisions
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{{Creutzfeldt-Jakob disease}} | {{Creutzfeldt-Jakob disease}} | ||
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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]]. Further investigation can then be performed to support the diagnosis. | The diagnosis of CJD is suspected when there are typical clinical symptoms and signs such as rapidly progressing dementia with [[myoclonus]]. Further investigation can then be performed to support the diagnosis. | ||
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[[Category:Transmissible spongiform encephalopathies]] | [[Category:Transmissible spongiform encephalopathies]] | ||
[[Category:Needs content]] | [[Category:Needs content]] | ||
Revision as of 20:42, 4 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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Diagnosis |
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Treatment |
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Creutzfeldt-Jakob disease laboratory findings On the Web |
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Risk calculators and risk factors for Creutzfeldt-Jakob disease laboratory findings |
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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. Further investigation can then be performed to support the diagnosis.
Cerebrospinal Fluid
- Analysis for 14-3-3 protein