Neuropsychiatric Disturbance in Huntington’s Disease: Approach to Management

INTRODUCTION: Huntington’s Disease (HD) is an autosomal dominant, neurodegenerative condition with a prevalence of 10.6-13.7 per 100,000, caused by the trinucleotide CAG (cytosine, adenine, guanine) repeat expansion in the HTT gene. HD is characterized by a range of motor, cognitive, and psychiatric...

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Detalles Bibliográficos
Autores principales: Jay, J., Kumar, V., Bidkhanian, P., Garrels, E., Segal, Y., Susaimanickam, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Abstract
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567710/
http://dx.doi.org/10.1192/j.eurpsy.2022.1208

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