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Huntington's disease

Huntington's disease is a disorder passed down through families in which certain nerve cells in the brain waste away, or degenerate.

  • Alternative Names

    Huntington chorea

  • Causes, incidence, and risk factors

    American doctor George Huntington first described the disorder in 1872.

    Huntington's disease is caused by a genetic defect on chromosome #4. The defect causes a part of DNA, called a CAG repeat, to occur many more times than it is supposed to. Normally, this section of DNA is repeated 10 to 35 times. But in persons with Huntington's disease, it is repeated 36 to 120 times.

    As the gene is passed on from one generation to the next, the number of repeats - called a CAG repeat expansion - tend to get larger. The larger the number of repeats, the greater your chance of developing symptoms at an earlier age. Therefore, as the disease is passed along in families, it becomes evident at younger and younger ages.

    There are two forms of Huntington's disease. The most common is adult-onset Huntington's disease. Persons with this form usually develop symptoms in their mid 30s and 40s.

    An early-onset form of Huntington's disease accounts for a small number of cases and begins in childhood or adolescence. Symptoms may resemble those of Parkinson's disease with rigidity, slow movements, and tremor.

    If one of your parents has Huntington's disease, you have a 50% chance of getting the gene for the disease. If you get the gene from your parents, you will develop the disease at some point in your life, and can pass it onto your children. If you do not get the gene from your parents, you cannot pass the gene onto your children.

  • Symptoms

    Behavior changes may occur before movement problems, and can include:

    Abnormal and unusual movements include:

    Dementia that slowly gets worse, including:

    • Loss of memory
    • Loss of judgment
    • Speech changes
    • Personality changes
    • Disorientation or confusion

    Additional symptoms that may be associated with this disease:

    Symptoms in children:

    • Rigidity
    • Slow movements
    • Tremor
  • Signs and tests

    The doctor will perform a physical exam and may ask questions about the patient's family history and symptoms. A neurological exam will also be done. The doctor may see signs of:

    • Dementia
    • Abnormal movements
    • Abnormal reflexes
    • "Prancing" and wide walk
    • Hesitant speech or poor enunciation

    A head CT scan may show loss of brain tissue, especially deep in the brain.

    Other tests that may show signs of Huntington's disease include:

    DNA marker studies may be available to determine whether you carry the gene for Huntington's disease.

  • Treatment

    There is no cure for Huntington's disease, and there is no known way to stop the disease from getting worse. The goal of treatment is to slow down the course of the disease and help the person function for as long and as comfortably as possible.

    Medications vary depending on the symptoms. Dopamine blockers may help reduce abnormal behaviors and movements. Drugs such as haloperidol, tetrabenazine, and amantadine are used to try to control extra movements. There has been some evidence to suggest that co-enzyme Q10 may also help slow down the course of the disease.

    Depression and suicide are common among persons with Huntington's disease. It is important for all those who care for a person with Huntington's disease to monitor for symptoms and treat accordingly.

    As the disease progresses, patients will need assistance and supervision. They may eventually need 24-hour care.

  • Support Groups

    Huntington's Disease Society of America - www.hdsa.org

  • Expectations (prognosis)

    Huntington's disease causes disability that gets worse over time. Persons with this disease usually die within 15 to 20 years. The cause of death is often infection, although suicide is also common.

    It is important to realize that the disease affects everyone differently. The number of CAG repeats may determine the severity of symptoms. Persons with few repeats may have mild abnormal movements later in life and slow disease progression, while those with a large number of repeats may be severely affected at a young age.

  • Complications
    • Loss of ability to care for self
    • Loss of ability to interact
    • Injury to self or others
    • Increased risk of infection
    • Depression
    • Death
  • Calling your health care provider

    Call your health care provider if you develop symptoms of this disorder.

  • Prevention

    Genetic counseling is advised if there is a family history of Huntington's disease. Experts also recommend genetic counseling for couples with a family history of this disease who are considering having children.

  • References

    Lang A. Other movement disorders. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier;2007:chap 434.

Review Date: 6/24/2009

Reviewed By: David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; and Daniel B. Hoch, PhD, MD, Assistant Professor of Neurology, Harvard Medical School, Department of Neurology, Massachusetts General Hospital. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997- 2014 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.
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