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Creutzfeldt-Jakob disease (CJD) is a form of spongiform encephalopathy which is caused by an abnormal protein called ‘prion’.1 It presents mainly as rapidly progressive dementia; myoclonus; visual problems; and dysfunction in cerebellar, pyramidal or extrapyramidal systems; and akinetic mutism.2
The premortem diagnosis of CJD is based on clinical features and paraclinical procedures, including brain MRI, electroencephalography (EEG) …
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