Creutzfeldt-Jakob disease

Creutzfeldt-Jakob disease


CJD is one of several prion diseases including; scrapie, BSE, and Kuru.

There are important differences between sporadic (aka classic) CJD and variant CJD which are summarised in the table below.

vCJDCJD
Duration (from onset of symptoms to death)Longer, a year or moreShorter, few months
SymptomsPsychiatric and behavioural only later neurologicalPresents neurologically
MRIPulvinar signBilateral anterior basal ganglia high signal
EEGGeneralised slowingBiphasic and triphasic waves 1-2 per second
OriginInfected meat productsGenetic mutation (bad luck)
Age of onsetYounger people (age 25-30)Old people (age 55-65)