Journal Basic Info
- Impact Factor: 1.809**
- H-Index: 6
- ISSN: 2474-1655
- DOI: 10.25107/2474-1655
Major Scope
- Cardiology
- Lung Cancer
- Physical Medicine & Rehabilitation
- Child Birth
- Radiology Cases
- Infectious Disease
- Molecular Biology
- Chronic Disease
Abstract
Citation: Ann Clin Case Rep. 2019;4(1):1764.DOI: 10.25107/2474-1655.1764
Misdiagnosis of an Atypical Creutzfeldt-Jakob Disease: Analysis of One Case in China and Review of the Literature
Mengqi Zhanga, Zigao Wangb, Lijie Duana and Hengbing Zua
Department of Neurology, Jinshan Hospital, Fudan University, China
Department of Neurology, Huashan Hospital, Fudan University, China
*Correspondance to: Hengbing Zua
PDF Full Text Case Report | Open Access
Abstract:
Creutzfeldt-Jakob Disease (CJD) is a fatal and infectious disease, which usually has atypical clinical symptoms include rapidly progressive dementia, myoclonus, pyramidal/extrapyramidal, visual, and akinetic mutism. In this report, we present an atypical sporadic Creutzfeldt-Jakob disease patient who was first misdiagnosed as encephalitis or brucellosis. In clinical study, for atypical CJD, it is very important to increase diagnosis accuracy and decrease misdiagnosis of CJD.
Keywords:
Creutzfeldt-Jakob disease; Prion protein; Dementia
Cite the Article:
Zhanga M, Wangb Z, Duana L, Zua H. Misdiagnosis of an Atypical Creutzfeldt- Jakob Disease: Analysis of One Case in China and Review of the Literature. Ann Clin Case Rep. 2019; 4: 1764.
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