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Huntington's disease: Neuropsychiatric manifestations of Huntington's disease

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Authors

Goh, Anita
Wibawa, Pierre
Loi, Samantha
Walterfang, Mark
Velakoulis, Dennis
Looi, Jeffrey

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Publisher

Sage Publications Inc

Abstract

Objectives: Huntington’s disease (HD) is a profoundly incapacitating, and ultimately fatal, neurodegenerative disease. HD is presently incurable, so the current goal is to allow affected individuals to live as well as possible with the illness, to maximise functional independence and quality of life for the person with HD, their carers and family members. This clinical update review focuses on the common neuropsychiatric manifestations in HD, and outlines and evaluates the various neuropsychiatric facets of HD, including the aetiology, symptoms and diagnosis. Conclusions: Neuropsychiatric symptoms can precede the classic motor clinical symptoms of HD (prodromal HD) by decades, and cause significant functional impairment. HD provides key insights and understanding into the organic psychiatric disorders, including contemporary clinical insights into the process of neurodegeneration and manifestation of neuropsychiatric symptoms.

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Citation

Source

Australasian Psychiatry

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Restricted until

2099-12-31