Finto: MeSH: Creutzfeldt-Jakob Syndrome

Infections > Central Nervous System Infections > Prion Diseases > Creutzfeldt-Jakob Syndrome

Nervous System Diseases > Central Nervous System Diseases > Central Nervous System Infections > Prion Diseases > Creutzfeldt-Jakob Syndrome

Nervous System Diseases > Neurodegenerative Diseases > Prion Diseases > Creutzfeldt-Jakob Syndrome

Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Dementia > Creutzfeldt-Jakob Syndrome

Mental Disorders > Neurocognitive Disorders > Dementia > Creutzfeldt-Jakob Syndrome

Creutzfeldt-Jakob Syndrome

A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))

1991; use JAKOB-CREUTZFELDT SYNDROME 1981-1990, use CREUTZFELDT-JAKOB DISEASE 1969-1980

http://www.yso.fi/onto/mesh/D007562

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