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Familial Creutzfeldt–Jakob Disease

1 Apr 2019

Abstract excerpt

Creutzfeldt–Jakob disease (CJD) belongs to a group of prion disease that is caused by abnormally folded proteins and is clinically characterized by rapidly progressive cognitive decline, gait abnormalities, and myoclonus. Familial CJD is very rare and is described only in few families around the world. We report a case with rapidly progressive cognitive decline, ataxia, and myoclonus, with a history of several...

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PMID: 31007442
DOI: 10.4103/aian.aian_441_18

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