An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease.


A 59-year-old Japanese man presented with depressed mood, insomnia, abnormal behavior and dementia. Visual and gait disturbance with ataxia also developed. Diffusion-weighted MRI showed widespread regions of hyperintensity in the bilateral cerebral cortex. The patient died at 62 after a progressive clinical course of 32 months. Myoclonus, periodic sharp… (More)
DOI: 10.1111/j.1440-1789.2010.01181.x


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