Creutzfeldt-Jakob disease physical examination: Difference between revisions

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*:* Akinetic mutism
*:* Akinetic mutism


PLUS
Positive result on one of the following laboratory tests:
* Typical [[EEG]] (periodic sharp wave complexes) during an illness of any duration and/or
* A positive 14-3-3 [[cerebrospinal fluid]] (CSF) assay in patients with a disease duration of less than 2 years and/or
* Magnetic resonance imaging (MRI): high signal abnormalities in [[caudate nucleus]] and/or [[putamen]] on diffusion-weighted imaging (DWI) or fluid attenuated inversion recovery (FLAIR).
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 02:30, 17 February 2014

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Creutzfeldt-Jakob disease Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Myoclonus, extrapyramidal signs and cerebellar signs are the most common physical findings in CJD.[1]

Physical Examination

Neurologic

  • Diagnosis of Creutzfeldt Jakob disease is probable if following criteria are fulfilled:
  • Rapidly progressive dementia plus any 2 of the following features
    • Myoclonus
    • Visual or cerebellar signs
    • Pyramidal and/or extrapyramidal signs
    • Akinetic mutism

PLUS Positive result on one of the following laboratory tests:

  • Typical EEG (periodic sharp wave complexes) during an illness of any duration and/or
  • A positive 14-3-3 cerebrospinal fluid (CSF) assay in patients with a disease duration of less than 2 years and/or
  • Magnetic resonance imaging (MRI): high signal abnormalities in caudate nucleus and/or putamen on diffusion-weighted imaging (DWI) or fluid attenuated inversion recovery (FLAIR).

References

  1. Rabinovici, GD.; Wang, PN.; Levin, J.; Cook, L.; Pravdin, M.; Davis, J.; DeArmond, SJ.; Barbaro, NM.; Martindale, J. (2006). "First symptom in sporadic Creutzfeldt-Jakob disease". Neurology. 66 (2): 286–7. doi:10.1212/01.wnl.0000196440.00297.67. PMID 16434680. Unknown parameter |month= ignored (help)

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