Huntington's Disease: Two-Year Observational Follow-Up of Executive Function Evaluation with CNS Vital Signs Test in an Adult Patient

Huntington's disease (HD) is a genetic, degenerative, and progressive central nervous system disease. It is characterized by motor abnormalities and cognitive and psychiatric symptoms. Objective. To describe the precise degree of clinical severity of patients with HD through a new neurocognitiv...

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Bibliographic Details
Main Authors: Anna Lucia Spear King, Alexandre Martins Valença, Adriana Cardoso de Oliveira e Silva, Ana Claudia Cerqueira, Lígia Maria Chaves Ferraz, Antonio Egidio Nardi
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2011/385894