Creutzfeldt-Jakob disease (CJD), which is caused by prion scrapie protein, is a rare, chronic, transmissible and fatal disease. Clinical manifestations of CJD include rapidly progressive dementia, cerebellar ataxia, v...
Creutzfeldt-Jakob disease (CJD) is a rare but fatal neurodegenerative prion disease. Classic CJD comprises a clinical triad of rapidly progressive dementia, myoclonus, and EEG abnormality. At initial presentation, thi...
Human prion disease is a rare,uniformly fatal neurodegenerative disorder.Its precise pathogenesis is obscure.The clinical profile of the disease differs among its various forms.There are no definitive diagnostic tests...