Huntington Disease(Huntington Chorea; HD)
by
Cynthia M. Johnson, MA DefinitionHuntington disease (HD) is a genetic problem of the brain. It causes the body to move in ways that the person cannot control. It also causes thinking problems that get worse over time. CausesHD is caused by a faulty gene. All people who inherit the faulty gene may get HD. Risk FactorsThe chance of getting HD is higher in those who have people in their family who have it. SymptomsProblems often start between 30 to 50 years of age. They are mild at first before they get worse. Problems may be:
DiagnosisThe doctor will ask about your symptoms and health history. You will be asked whether you have other people in your family with HD. A physical exam will be done. Cognitive tests may also be done. Blood tests will be done to look for the faulty gene. Images may be taken to support the diagnosis. This can be done with:
TreatmentThere is no cure for HD. Symptoms can only be managed. MedicationsMedicine may be given to ease body movements. These may be:
SupportCounseling and support groups can help a person learn how to cope with HD. PreventionHD cannot be prevented in a person who has the faulty gene. RESOURCES:Hereditary Disease Foundation http://www.hdfoundation.org Huntington Disease Society of America http://www.hdsa.org CANADIAN RESOURCES:Health Canada https://www.canada.ca Huntington Society of Canada http://www.huntingtonsociety.ca References:Armstrong MJ, Miyasaki JM. Evidence-based guideline: pharmacologic treatment of chorea in Huntington disease: report of the guideline development subcommittee of the American Academy of Neurology. Neurology. 2012 Aug 7;79(6):597-603. Fast facts about HD. Huntington's Disease Society of America website. Available at: ...(Click grey area to select URL) Accessed October 18, 2019.
Huntington disease. EBSCO DynaMed website. Available at:
https://www.dynamed.com/condition/huntington-disease. Updated July 24, 2018. Accessed October 18, 2019.
Huntington's disease information page. National Institute of Neurological Disorders and Stroke website. Available at: ...(Click grey area to select URL) Updated March 27, 2019. Accessed October 18, 2019. Kringlen G, Kinsley L, et al. The Impact of Family History on the Clinical Features of Huntington's Disease. J Huntingtons Dis. 2017;6(4):327-335. Last reviewed September 2019 by
EBSCO Medical Review Board
Rimas Lukas, MD Last Updated: 8/26/2020 |
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