A Unique Case of Genetic Creutzfeldt-Jakob Disease (E200K Mutation) with CSF-restricted Anti Myelin Oligodendrocyte Glycoprotein Antibody.

Abstract excerpt

Creutzfeldt-Jakob disease (CJD) is a rare, fatal neurodegenerative disorder that can share clinicoradiologic features with autoimmune cortical encephalitis (CE); however, the pathological significance of myelin oligodendrocyte glycoprotein (MOG)-IgG, which is one of the causes of CE, has not yet been explored in the context of CJD. We herein present the case of a man in his mid-70s with a family history of CJD...

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