Abstract
Background The clinical and pathological heterogeneity of progressive supranuclear palsy (PSP) is well established. Even with a well-defined clinical phenotype and a thorough laboratory workup, PSP can be misdiagnosed, especially in its early stages. Case Report A 52-year-old woman, who we initially diagnosed with a behavioral variant of frontotemporal dementia developed parkinsonian features, which then progressed to gait instability and gaze abnormality. Conclusions We report herein a pathologically confirmed case of PSP presenting with behavioral changes including agitation and irritability, which eventually led to the cardinal symptoms of progressive supranuclear palsy. © 2010 Korean Neurological Association.
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Han, H. J., Kim, H., Park, J. H., Shin, H. W., Kim, G. U., Kim, D. S., … Kim, Y. J. (2010). Behavioral changes as the earliest clinical manifestation of progressive supranuclear palsy. Journal of Clinical Neurology (Korea), 6(3), 148–151. https://doi.org/10.3988/jcn.2010.6.3.148
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