Resumo

RODRIGUEZ PUPO, Jorge Michel et al. Update on Huntington Disease. CCM [online]. 2013, vol.17, suppl.1, pp.546-557. ISSN 1560-4381.

Huntington Disease is a neurodegenerative disorder transmitted as an autosomal dominant trait. Selective neuronal loss in the striatum leads to chorea and cognitive impairment. It is a progressive disease with onset in midlife, which chronically evolves over many years and for which no curative treatment is available today. A review on the current knowledge of Huntington Disease   was carried out. Etiopathogenic, clinical, diagnostic methods and treatment options   were included.

Palavras-chave : Huntington Disease; autosomal dominant; chorea; chronic; progressive.

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