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Behavioral Changes as the Earliest Clinical Manifestation of Progressive Supranuclear Palsy
Journal of Clinical Neurology ; : 148-151, 2010.
Article in English | WPRIM | ID: wpr-207094
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.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Population Characteristics / Supranuclear Palsy, Progressive / Parkinsonian Disorders / Dihydroergotamine / Frontotemporal Dementia / Gait Limits: Female / Humans Language: English Journal: Journal of Clinical Neurology Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Population Characteristics / Supranuclear Palsy, Progressive / Parkinsonian Disorders / Dihydroergotamine / Frontotemporal Dementia / Gait Limits: Female / Humans Language: English Journal: Journal of Clinical Neurology Year: 2010 Type: Article