Creutzfeldt-Jakob disease overview
Creutzfeldt-Jakob disease Microchapters |
Differentiating Creutzfeldt-Jakob disease from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Creutzfeldt-Jakob disease overview On the Web |
American Roentgen Ray Society Images of Creutzfeldt-Jakob disease overview |
Risk calculators and risk factors for Creutzfeldt-Jakob disease overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Creutzfeldt-Jakob disease is a very rare and incurable degenerative neurological disorder (braindisease) that is ultimately fatal. Among the types of transmissible spongiform encephalopathy found in humans, it is the most common.
Diagnosis
Laboratory Findings
The diagnosis of CJD is suspected when there are typical clinical symptoms and signs such as rapidly progressing dementia with myoclonus. Analysis of CSF for 14-3-3 protein is done to establish diagnosis.