Creutzfeldt-Jakob disease diagnostic study of choice

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{Creutzfeldt-Jakob disease}} Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Biopsy of the brain tissue is the definitive diagnostic test for Creutzfeldt-Jakob disease(CJD), but is not usually performed. EEG findings are not diagnostic of CJD, but may help in the diagnosis of CJD. Typical EEG findings in Creutzfeldt-Jakob disease include periodic biphasic or triphasic sharp wave complexes (PSWCs). Periodic synchronous discharges (PSDs) occur either before or in synchronicity with myoclonus.

Other Diagnostic Studies

Biopsy

  • Deposits of prion protein (scrapie), PrPSc, can be found in the skeletal muscle and/or the spleen (approximately 30% of cases).
  • Diagnosis of vCJD can be supported by biopsy of the tonsils, which harbor significant amounts of PrpSc.
  • Biopsy of the brain tissue is the definitive diagnostic test, but is not usually performed.

Gallery

References

  1. 1.0 1.1 1.2 1.3 "Public Health Image Library (PHIL)".


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