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Diagnostic criteria for sporadic CJD

Authoring team

The diagnostic criteria for (classical) sporadic Creutzfeldt-Jacob disease are:

  • definite diagnosis, any of the following:
    • neuropathologically confirmed
    • positive PrP Western blot
    • presence of scrapie-associated fibrils

  • probable diagnosis:
    • progressive dementia
    • typical EEG
    • two or more of:
      • myoclonus
      • visual or cerebellar signs
      • pyramidal/extrapyramidal signs
      • akinetic mutism

  • possible diagnosis:
    • progressive dementia
    • two of:
      • myoclonus
      • visual or cerebellar signs
      • pyramidal/extrapyramidal signs
      • akinetic mutism
    • duration <2 years

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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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