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Huntington's Disease

(Huntington Chorea; HD)

Definition

Huntington's disease (HD) is an inherited disorder that affects the brain. HD causes slow, progressive degeneration of nerve cells in certain areas of the brain. Eventually, HD results in:
  • Abnormal body movements
  • Gradual deterioration or loss of intellectual abilities (dementia)
  • Behavior problems

Causes

A faulty gene on chromosome #4 causes HD. All people who inherit the faulty gene may eventually develop HD.

Risk Factors

These factors increase your chance of developing HD:
  • Family members with HD: Each person whose parent has HD has a 50% chance of inheriting the disorder.
  • Age: Onset of symptoms range from 35-50 years old. Juvenile cases occur in people less than 20 years of age.

Symptoms

Symptoms are mild at first and are often barely noticeable but usually worsen over 15-20 years.
Physical symptoms may include:
  • Abnormal body movements that worsen over time, including:
    • Sudden jerks or uncontrolled movements of the limbs or trunk
    • Facial grimacing
    • Continuous need to turn head and shift gaze
    • Walking that is unsteady or dance-like
  • Difficulty with eating, dressing, sitting, and caring for oneself
  • Difficulty swallowing
  • Grunting or poor articulation of speech
  • Weight loss
Intellectual and emotional symptoms may include:
  • Trouble with attention and awareness
  • Confusion or disorientation
  • Loss of memory
  • Loss of judgment
  • Loss of ability to think rationally
  • Irritability and moodiness
  • Depression (common)
  • Anxiety
  • Social withdrawal or antisocial behavior
  • Irresponsible behavior
  • Obsessive-compulsive behavior
  • Personality changes
  • Psychosis—a severe emotional and behavioral disorder that often interferes with a person's ability to relate to others and to function in daily life
  • Paranoia—a mental disorder that involves feelings of being watched, followed, or harmed by others
  • Hallucinations—the perception of a thing or person that is not present
Ultimately, HD can:
  • Cause the loss of the physical and mental ability to care for oneself
  • Cause severe disability, making full-time or nursing home care necessary
  • Result in death, often due to a fall or pneumonia

Diagnosis

The doctor will ask about your symptoms and medical history (including family medical history). A physical exam will be done. Tests may include:
CT Scan of the Head
CT Scan of the Head
Copyright © Nucleus Medical Media, Inc.
There is a test that can determine if a person has inherited the gene for HD. This test may help to make the diagnosis of HD. It may also help to determine if a person has inherited the HD gene before symptoms appear. Genetic counseling is recommended before taking this test to review risks and benefits.

Treatment

There is no cure for HD. Treatment aims to help control symptoms.

Medications

Drugs can help control abnormal movements and emotional symptoms of HD. These include:
  • Tetrabenazine
  • Sedatives or minor tranquilizers, such as benzodiazepines
  • Major tranquilizers, like haloperidol or phenothiazine
  • Antidepressants

Physical Fitness

Staying physically active helps people with HD to function better and longer. Often physical and occupational therapy may be of some benefit.

Prevention

There is no way to prevent the onset of HD if a person has inherited the gene for the disorder. Medicines aimed at slowing and treating the disease progression are being studied. A prospective parent with HD or a family history of HD can seek genetic counseling when deciding whether or not to have children. Genetic counseling is extremely important since children of parents with HD will have a 50% chance of inheriting the condition.

RESOURCES

Hereditary Disease Foundation http://www.hdfoundation.org/

Huntington Disease Society of America http://www.hdsa.org/

International Huntington Association http://www.huntington-assoc.com/

CANADIAN RESOURCES

Health Canada http://www.hc-sc.gc.ca/

Huntington Society of Canada http://www.huntingtonsociety.ca/

References

Agarwal P. Huntington disease. MedLink Neurology website. Available at: http://www.medlink.com/medlinkcontent.asp . Accessed July 1, 2009.

Aminoff M. Nervous system disorders. McPhee S, Papadakis M, Tierney L. Current Surgical Diagnosis and Treatment. 12th ed. New York, NY: McGraw-Hill; 2003; chap 24.

Beers MH. The Merck Manual of Medical Information . 2nd ed. London, England: Simon and Schuster, Inc; 2003.

DynaMed Editorial Team. Huntington disease. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed/what.php . Updated July 9, 2010. Accessed November 17, 2010.

Mestre T, Ferreira J, Coelho MM, et al. Therapeutic interventions for symptomatic treatment in Huntington's disease. Cochrane Database Syst Rev . 2009;8(3):CD006456.

NINDS Huntington's Disease information page. National Institute of Neurological Disorders and Stroke website. Available at: http://www.ninds.nih.gov/disorders/huntington/huntington.htm . Accessed July 1, 2009

Revision Information

  • Reviewer: Rimas Lukas, MD
  • Review Date: 09/2012 -
  • Update Date: 00/91/2012 -

This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.

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