Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype
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Creutzfeldt-Jakob disease (CJD) is a prion disease, usually presented with memory loss, ataxia, dementia, myoclonus, involuntary movements and psychiatric problems. D178N-homozygous 129M genotype has been recognized in the diagnosis of fatal familial insomnia ... ...