A case report of sporadic Creutzfeldt–Jakob disease presenting with progressive opsoclonus–myoclonus–ataxia-Plus (OMAS-Plus) phenotype
ABSTRACT Background Sporadic Creutzfeldt–Jakob disease (sCJD) is a rapidly progressive prion disorder whose heterogeneous manifestations may overlap with potentially treatable neurological conditions. We report an atypical sCJD phenotype dominated by progressive dysarthria and an opsoclonus–myoclonus–ataxia-plus (OMAS-...