A 75-year-old woman presented with gradual memory loss and disorientation during the previous year. Despitescoring 22 points on the MMSE, she remained polite. Brain MRI indicated no abnormalities, however, SPECTrevealed relative hypoperfusion in the posterior cingulate gyrus. She was diagnosed with Alzheimer’s diseaseand began therapy with donepezil. Within four months, rapid cognitive impairment required hospitalization. Twoweeks later, myoclonus developed, resulting in akinetic mutism. Following admission, an MRI revealed hyperintense areas in the right basal ganglia and cerebral cortex, as well as periodic synchronous discharges on EEG. CSFanalysis revealed positive 14-3-3 protein and RT-QUIC results. A prion protein-encoding gene study revealed sporadic Creutzfeldt–Jakob disease with methionine homozygosity at codon 129. Initially, diagnosed with Alzheimer’s disease, rapid symptom development became apparent 16 months later, suggesting concurrent sporadicCreutzfeldt–Jakob disease.
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