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Medical Health Encyclopedia
Huntington's disease
From Healthscout's partner site on chronic pain, HealthCentral.com
Huntington chorea 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
Calling your health care provider Call your health care provider if you develop symptoms of this disorder.
Review Date: 06/24/2009 A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). ![]() | ||||||||||||||
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