Creutzfeldt-Jakob disease laboratory findings: Difference between revisions
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==Overview== | ==Overview== | ||
==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. | ||
===Cerebrospinal Fluid=== | ===Cerebrospinal Fluid=== | ||
* Analysis for [[14-3-3 protein]] | * Analysis for [[14-3-3 protein]] | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 18:04, 20 November 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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Case Studies |
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Creutzfeldt-Jakob disease laboratory findings On the Web |
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American Roentgen Ray Society Images of Creutzfeldt-Jakob disease laboratory findings |
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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]
Overview
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