Revisiting the neuropsychiatry of Huntington’s disease

Antonio Lucio Teixeira, Leonardo Cruz De Souza, Natalia Pessoa Rocha, Erin Furr-Stimming, Edward C. Lauterbach

Producción científica: Articlerevisión exhaustiva

25 Citas (Scopus)

Resumen

Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease classified under the choreas. Besides motor symptoms, HD is marked by cognitive and behavioral symptoms, impacting patients’ functional capacity. The progression of cognitive impairment and neuropsychiatric symptoms occur in parallel with neurodegeneration. The nature of these symptoms is very dynamic, and the major clinical challenges include executive dysfunction, apathy, depression and irritability. Herein, we provide a focused updated review on the cognitive and psychiatric features of HD.

Idioma originalEnglish (US)
Páginas (desde-hasta)261-266
Número de páginas6
PublicaciónDementia e Neuropsychologia
Volumen10
N.º4
DOI
EstadoPublished - oct 1 2016
Publicado de forma externa

ASJC Scopus subject areas

  • Sensory Systems
  • Neurology
  • Geriatrics and Gerontology
  • Clinical Neurology
  • Cognitive Neuroscience

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