Comatose within 6 weeks but still alive after 3 years Creutzfeldt‐Jakob disease with unusual progression

摘要

Creutzfeldt‐Jakob disease (CJD) should still be considered in a patient presenting with rapidly progressive dementia and negative CSF 14‐3‐3 protein and RT‐QulC. Treatable causes of encephalopathy must be ruled out. Neurodegenerative diseases must also be considered.