Table 1.
vCJD | sporadic CJD | |
---|---|---|
Mean age at death | 30 years | 65 years |
Mean duration of the disease | 14 months | 6 months |
Clinical symptoms at the onset of disease | dysesthesia, behavioral changes | memory disorder, ataxia |
EEG | non-typical | 66% PSWCs |
Detection of 14-3-3 protein in cerebrospinal fluid | 50% | 94% |
Magnetic resonance tomography | hyperintensities in the thalamus, 'pulvinar sign' | hyperintensities in the basal ganglia |
Codon 129 genotype | MM | MM, MV, VV |
Lymphatic system | PrPTSE | no PrPTSE |
Neuropathologic characteristics | 'florid plaques' | variable, no 'florid plaques' |
PSWCs = Periodic sharp and slow wave complexes.