Creutzfeldt-Jakob Disease Presenting with Dementia and Mimic a Stroke During One Year: Case Report and Review of Literatures

Creutzfeldt-Jakob disease (CJD) is a progressive and fatal prion disease in human and its annual incidence is estimated one per million. Sporadic form of CJD is the most common form of the disease that involved 85% of cases. We presented two cases of CJD with the different clinical presentation; a 5...

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Bibliographic Details
Published inGalen Vol. 8; p. e1357
Main Authors Vakilian, Alireza, Fekri, Mohaddaseh, Farahmand, Habib
Format Journal Article
LanguageEnglish
Published Iran Salvia Medical Sciences Ltd 2019
Subjects
Case Report
Creutzfeldt-Jakob Disease
Dementia
Incidence
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Summary:Creutzfeldt-Jakob disease (CJD) is a progressive and fatal prion disease in human and its annual incidence is estimated one per million. Sporadic form of CJD is the most common form of the disease that involved 85% of cases. We presented two cases of CJD with the different clinical presentation; a 58-year-old woman who referred with amnesia, depression and a 59-year-old woman with ataxia as her chief complaint. Based on the findings and roled-out the other differential diagnosis, the CJD was confirmed. Both of them died before 12 months after diagnosis. Although CJD is a rare disease with different clinical manifestation, it is considered as one the differential diagnosis of progressive dementia.
ISSN:2588-2767
2322-2379
DOI:10.31661/gmj.v8i0.1357