| alternative label
| - Syndrome de Creutzfeldt-Jakob
- Nouvelle variante de la maladie de Creutzfeldt-Jakob
- CJD (Creutzfeldt-Jakob Disease)
- Creutzfeldt Jacob Disease
- Creutzfeldt Jakob Disease
- Creutzfeldt Jakob Disease, Variant
- Disease, Creutzfeldt Jacob
- Encephalopathy, Subacute Spongiform
- Encéphalopathie spongiforme subaiguë
- Familial Creutzfeldt Jakob Disease
- Maladie de Creutzfeldt-Jakob familiale
- Variant Creutzfeldt-Jakob Disease
- CJD (Creutzfeldt Jakob Disease)
- Creutzfeldt Jakob Disease, Familial
- Disease, Creutzfeldt-Jakob
- Familial Creutzfeldt-Jakob Diseases
- MCJ (Maladie de Creutzfeldt-Jakob)
- Pseudosclérose spastique de Jakob
- V CJD (Variant Creutzfeldt Jakob Disease)
- variante-MCJ
- nv-MCJ (nouvelle variante de la Maladie de Creutzfeldt-Jakob )
- Creutzfeldt-Jakob Diseases, Familial
- Disease, Familial Creutzfeldt-Jakob
- Disease, Jakob-Creutzfeldt
- Jakob-Creutzfeldt Disease
- New Variant Creutzfeldt Jakob Disease
- Pseudo-sclérose spastique de Jakob
- Spongiform Encephalopathy, Subacute
- Syndrome, Creutzfeldt-Jakob
- nv-MCJ
- Creutzfeldt Jakob Syndrome
- Creutzfeldt-Jakob Disease
- Creutzfeldt-Jakob Disease, New Variant
- Creutzfeldt-Jakob Syndrome
- Encephalopathies, Subacute Spongiform
- Familial Creutzfeldt-Jakob Disease
- Jakob Creutzfeldt Disease
- New Variant Creutzfeldt-Jakob Disease
- Spongiform Encephalopathies, Subacute
- Syndrome, Jakob-Creutzfeldt
- Creutzfeldt Jakob Disease, New Variant
- Creutzfeldt-Jakob Disease, Familial
- Creutzfeldt-Jakob Disease, Variant
- Encéphalopathie spongiforme subaigüe
- Jacob Disease, Creutzfeldt
- Jakob Creutzfeldt Syndrome
- Jakob-Creutzfeldt Syndrome
- Subacute Spongiform Encephalopathies
- Subacute Spongiform Encephalopathy
- V-CJD (Variant-Creutzfeldt-Jakob Disease)
- Variant Creutzfeldt Jakob Disease
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| note
| - 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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