Problems often start between 30 to 50 years of age. They are mild at first before they get worse.
Problems may be:
- Changes in eye movements
- Moving without control
- Jerking movements of the arms, legs, face, or belly
- Problems making decisions
- Lack of emotion
- Mood swings
- Problems walking and swallowing
The 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:
- MRI scan
- CT scan
- SPECT scan
|MRI Scan of the Brain|
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a (Huntington Chorea; HD)
Hereditary Disease Foundation http://www.hdfoundation.org
Huntington Disease Society of America http://www.hdsa.org
Health Canada https://www.canada.ca
Huntington Society of Canada http://www.huntingtonsociety.ca
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: http://hdsa.org/wp-content/uploads/2015/03/HDSA%5FFast-Facts.pdf?23ef42. 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: http://www.ninds.nih.gov/disorders/huntington/huntington.htm. 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.