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Huntington's Disease

See Also:
Huntington's Disease: Introduction
Huntington's Disease: Causes & Risk Factors
Huntington's Disease: Signs & Symptoms
Huntington's Disease: Medical Tests & Diagnosis Methods
Huntington's Disease: Treatment Options

Treatment Options

Medications:
There is no cure or treatment to stop or reverse the course of Huntington’s disease and the medications may only help in keeping the clinical symptoms under control. Symptoms are treated as follows:

  • Treatment of depression also improves symptoms such as social withdrawal, lack of interest and sleep disturbance. It is treated with tricyclic antidepressants (amitriptyline, imipramine, desipramine, nortriptyline) and selective serotonin reuptake inhibitors (SSRIs) such as paroxetine, fluoxetine and sertraline.

  • Treatment of movement disorders helps in treatment of abnormal movements. It is treated with Tetrabenazine (Xenazine), haloperidol (eg Haldol) and fluphenazine (Modecate).

  • Symptoms such as antisocial behavior, irritability and psychosis are treated with Chlorpromazine (eg Largactil), sulpiride (eg Sulpitil), quetiapine (Seroquel), clozapine (eg Clozaril), risperidone (Risperdal) and leuprorelin acetate (12).

  • Treatment with lithium, valproate and carbamazepine can help as mood stabilizers (mania and bipolar disorders). Botulinum toxin can be used to treat dystonia and jaw clenching (13).

Communication:
Communication skills, memory and alternative communication can be improved with speech and language therapy. Speech therapy can also help overcome swallowing difficulties. The family of a person suffering from HD needs to exercise patience and be supportive in order to try alternative ways of communication if speech and organizing thought process is a problem (5).

Diet:
People suffering from HD are given a high calorie diet since they burn more calories by continuous movement and a close watch should be kept to avoid weight loss. Food should be easy to chew, swallow and digest.

Alternative feeding arrangements such as naso-gastric tube are made in later stages (5).

 

Physical and Occupational Therapy:
Regular exercise and physical therapy can keep muscles stronger, flexible and lessen the risk of falling. Since falls are always risky, special padding may be provided during walks to help protect against injury from falls. Ocupational therapy helps in coping with memory and increase concentration and can assist the patient with eating, dressing and hygiene challenges in later stages (5) & (14).

Prevention Methods
Huntington’s disease cannot be prevented. In families with a history of Huntington's Disease, a prenatal diagnostic test can be carried out to calculate the risk of developing the disease early in pregnancy. The tests are predictive and there are 50-50 chances of inheriting the disease. In case of a positive result, genetic counseling can explain to the parents about results of the tests and also the future course (12).

See Also:
Huntington's Disease: Introduction
Huntington's Disease: Causes & Risk Factors
Huntington's Disease: Signs & Symptoms
Huntington's Disease: Medical Tests & Diagnosis Methods
Huntington's Disease: Treatment Options

Article by Kona Vishnu, MS
Medical Writer,
OmniMedicalSearch.com

Sources:

  1. Huntington's Disease, Neurology Channel, July 2007.
  2. Overview of Huntington's Disease, WE MOVE - Worldwide Education and Awareness for Movement Disorders, April 2006.
  3. Huntington Disease, Medicinenet.com, April 2002.
  4. Huntington’s Disease – Causes/Genetics, WE MOVE - Worldwide Education and Awareness for Movement Disorders, April 2006.
  5. Huntington’s disease, NHS Direct, June 2007.
  6. Huntington's Disease: Hope Through Research, National Institute of Neurological Disorders and Stroke, May 2007.
  7. Huntington’s disease – Risk factors, MayoClinic.com, May 2007.
  8. Huntington’s Disease - Symptoms, Findings, and Clinical Course of Huntington's Disease, WE MOVE - Worldwide Education and Awareness for Movement Disorders, April 2006.
  9. Huntington’s Disease - Neurobehavioral Changes, WE MOVE - Worldwide Education and Awareness for Movement Disorders, April 2006.
  10. Huntington’s Disease – Cognitive Decline, WE MOVE - Worldwide Education and Awareness for Movement Disorders, April 2006.
  11. Huntington’s Disease –Motor Disturbances, WE MOVE - Worldwide Education and Awareness for Movement Disorders, April 2006.
  12. Huntington’s disease, netdoctor.co.uk, Dr.Linda Appai-Kubi and Dr. K. Ray Chaudhari, September 2001.
  13. Huntington's Disease-Treatment, Prognosis, Neurology Channel, July 2007
  14. Huntington’s disease – Treatment, MayoClinic.com, May 2007.

Huntington's Disease is sometimes misspelled as huntington diseas, huntingdons disease, huntingdon disease and huntings disease .

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Page Last Modified:
12/02/2010