Huntington disease (HD or Huntington chorea) is a condition where nerve cells in the brain region called the striatum are lost. It is a condition that runs in families (genetic). A child of a person with Huntington disease has a 1 in 2 chance of inheriting the gene that causes this disease. If you have the gene, you will get the disease and you can pass it on to your children.
The gene is present from birth. But the illness often does not appear until mid-life. Juvenile Huntington disease appears before the age of 20. Most people with this condition don't die from the disease. Instead they die from other health problems, such as injuries from falls, infections, choking, or pneumonia. Because different areas of the brain may be affected in different people, your symptoms may not be the same as those of your parents.
HD symptoms vary from person to person. But there are generally three stages everyone goes through:
- In the early stage of HD, the person often has mood problems, such as depression or irritability. The person may not function well at home or work.
- In the second stage, the movement disorder may become more apparent. The person may have problems with talking or trouble swallowing.
- In the final stage, the person with HD becomes totally dependent on others for all care. The person also is unable to walk or speak and loses a lot of weight. But generally, the person with HD is still able to understand language and is aware of family and friends.
Symptoms of HD include:
- Rapid, jerky, or writhing movements (chorea)
- Unsteady gait
- Trouble with speech, swallowing, balance, and walking
- Loss of mental abilities and memory, confusion, and inability to concentrate
- Emotional changes, such as mood swings, irritability, depression, anxiety, anger, or social withdrawal
- Hallucinations
- Weight loss
There is no known cure for this disease. Medicine can be given to control some of the symptoms.
Children of a person with this illness can be tested to find out if they have the gene. Ask your doctor to refer you to a genetic counselor to talk about the pros and cons of testing.