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  • Creutzfeldt-Jakob Syndrome - »õâ 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))
    Synonyms : CJD, CJD (Creutzfeldt-Jakob Disease), Creutzfeldt-Jakob Disease, Creutzfeldt-Jakob Disease, Familial, Creutzfeldt-Jakob Disease, New Variant, Familial Creutzfeldt-Jakob Disease, Jakob-Creutzfeldt Disease, Jakob-Creutzfeldt Syndrome, CJD Variant (V CJD)
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 4
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