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单词 Creutzfeldt-Jakob Syndrome
释义

Creutzfeldt-Jakob Syndrome


《英文msh词典》Creutzfeldt-Jakob Syndrome
[主题词] Creutzfeldt-Jakob Syndrome
[同义词] CJD Variant (V-CJD)
[同义词] New Variant Creutzfeldt-Jakob Disease
[同义词] Spongiform Encephalopathy,Subacute
[入口词] CJD
[入口词] CJD (Creutzfeldt-Jakob Disease)
[入口词] Creutzfeldt-Jakob Disease
[入口词] Creutzfeldt-Jakob Disease,Familial
[入口词] Creutzfeldt-Jakob Disease,New Variant
[入口词] Familial Creutzfeldt-Jakob Disease
[入口词] Jakob-Creutzfeldt Disease
[入口词] Jakob-Creutzfeldt Syndrome
[入口词] V-CJD (Variant-Creutzfeldt-Jakob Disease)
[入口词] CJD (Creutzfeldt Jakob Disease)
[入口词] CJD Variant (V CJD)
[入口词] CJD Variants (V-CJD)
[入口词] CJDs (Creutzfeldt-Jakob Disease)
[入口词] Creutzfeldt Jakob Disease
[入口词] Creutzfeldt Jakob Disease,Familial
[入口词] Creutzfeldt Jakob Disease,New Variant
[入口词] Creutzfeldt Jakob Syndrome
[入口词] Creutzfeldt-Jakob Diseases,Familial
[入口词] Disease,Creutzfeldt-Jakob
[入口词] Disease,Familial Creutzfeldt-Jakob
[入口词] Disease,Jakob-Creutzfeldt
[入口词] Encephalopathies,Subacute Spongiform
[入口词] Encephalopathy,Subacute Spongiform
[入口词] Familial Creutzfeldt Jakob Disease
[入口词] Familial Creutzfeldt-Jakob Diseases
[入口词] Jakob Creutzfeldt Disease
[入口词] Jakob Creutzfeldt Syndrome
[入口词] New Variant Creutzfeldt Jakob Disease
[入口词] Spongiform Encephalopathies,Subacute
[入口词] Subacute Spongiform Encephalopathies
[入口词] Subacute Spongiform Encephalopathy
[入口词] Syndrome,Creutzfeldt-Jakob
[入口词] Syndrome,Jakob-Creutzfeldt
[入口词] Variant,CJD (V-CJD)
[入口词] Variants,CJD (V-CJD)
[中文释义] 克-亚综合征
[英文释义] 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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