Delayed Huntington's disease diagnosis in two alcoholic patients with a family history of "Parkinson's disease".

نویسندگان

  • Joana Mesquita
  • Luísa Silva
  • Alvaro Machado
چکیده

To the Editor: Huntington’s disease is an autosomal dominant neurodegenerative disease characterized by a triad of symptoms and signs including movement disorder, cognitive impairment, and behavioral syndromes. As the earliest pathological changes in Huntington’s disease are in the associative portion of the striatum, the domains first affected by the disease may be cognitive and psychiatric rather than motor.

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عنوان ژورنال:
  • The Journal of neuropsychiatry and clinical neurosciences

دوره 22 4  شماره 

صفحات  -

تاریخ انتشار 2010