Objective: Progressive Supranuclear Palsy (PSP) is a rare degenerative condition of unknown etiology with an incidence of 1 to 5.3 per 100,000 individuals. It is characterized by Parkinsonism, gait impairments, dysphagia, abnormalities of extraocular movements, cognitive decline (i.e. memory, executive functioning), and psychiatric symptoms. The literature has reported a poor prognosis, with a mean age of survival of nine years after the onset of symptoms. Further, PSP is often misdiagnosed in most cases as Parkinson's disease, which results in delayed intervention, inadequate treatment, and substantial psychosocial distress. Research has focused primarily on the management of physical symptoms and pharmacological treatments. The purpose of this case study is to expand on the literature regarding PSP neuropsychological profile, assist in accurate diagnosis, and offer additional treatment options. Method: This case study is of a 68-year-old right handed, Caucasian, male with reported cognitive decline and functional deficits for the last three years. He...

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