• DOI:10.1097/NRL.0b013e31818967b8
• Corpus ID: 32110012

Huntington disease.

@article{Kernich2008HuntingtonD,
  title={Huntington disease.},
  author={Catherine Ann Kernich},
  journal={The neurologist},
  year={2008},
  volume={14 6},
  pages={
          399-400
        }
}

• C. Kernich
• Published 2008
• Psychology
• The neurologist

Adult-onset Huntington disease, the most common form of this disorder, usually appears in a person's thirties or forties. Early signs and symptoms can include irritability, depression, small involuntary movements, poor coordination, and trouble learning new information or making decisions. Many people with Huntington disease develop involuntary jerking or twitching movements known as chorea. As the disease progresses, these movements become more pronounced. Affected individuals may have trouble walking, speaking, and swallowing. People with this disorder also experience changes in personality and a decline in thinking and reasoning abilities. Individuals with the adult-onset form of Huntington disease usually live about 15 to 20 years after signs and symptoms begin.