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Definition: 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)) |
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Synonyms: - CJD
- CJD (Creutzfeldt Jakob Disease)
- CJD (Creutzfeldt-Jakob Disease)
- CJD Variant (V CJD)
- CJD Variant (V-CJD)
- CJD Variants (V-CJD)
- CJDs (Creutzfeldt-Jakob Disease)
- Creutzfeldt Jakob Disease
- Creutzfeldt Jakob Disease, Familial
- Creutzfeldt Jakob Disease, New Variant
- Creutzfeldt Jakob Syndrome
- Creutzfeldt-Jakob Disease
- Creutzfeldt-Jakob Disease, Familial
- Creutzfeldt-Jakob Disease, New Variant
- Creutzfeldt-Jakob Diseases, Familial
- Disease, Creutzfeldt-Jakob
- Disease, Familial Creutzfeldt-Jakob
- Disease, Jakob-Creutzfeldt
- Encephalopathies, Subacute Spongiform
- Encephalopathy, Subacute Spongiform
- Familial Creutzfeldt Jakob Disease
- Familial Creutzfeldt-Jakob Disease
- Familial Creutzfeldt-Jakob Diseases
- Jakob Creutzfeldt Disease
- Jakob Creutzfeldt Syndrome
- Jakob-Creutzfeldt Disease
- Jakob-Creutzfeldt Syndrome
- New Variant Creutzfeldt Jakob Disease
- New Variant Creutzfeldt-Jakob Disease
- Spongiform Encephalopathies, Subacute
- Spongiform Encephalopathy, Subacute
- Subacute Spongiform Encephalopathies
- Subacute Spongiform Encephalopathy
- Syndrome, Creutzfeldt-Jakob
- Syndrome, Jakob-Creutzfeldt
- V-CJD (Variant-Creutzfeldt-Jakob Disease)
- Variant, CJD (V-CJD)
- Variants, CJD (V-CJD)
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