Some individuals develop the symptoms of Huntington’s disease when they are very young, and also before the ages of twenty. It is also very common when people suffering from the disease are at the ages between twenty and forty years old. A common observation is that the earlier the symptoms can appear, the faster the disease will progresses. Some will also find it hard to keep their body still because of involuntary movement and having difficulty walking, and have a hard time speaking. A person’s thinking ability can and will also be affected due to the disease. Huntington’s disease also effects the behavior of people from getting angry, frustrated and can cause depression, which is very high with the disease. HTT is a gene involved and provides instructions for making a protein called Huntington. Although, it’s unknown it doe play an important role in the nerve cells (neurons) in the brain. The disease can be inherited in an autosomal dominant pattern. The chances of getting the disease is due to an affected parent that passes it …show more content…
There have been studies that have shown that there is no cure for Huntington’s disease, there is also no known way from stopping the disease from getting worse. As of now the main goal is to find it early and treatment is to slow the symptoms and help the person function for as long as possible. There are medications that help increase abnormal behaviors and movements. Death can also be a known factor from falling, any types of infection and complication related to the inability of not being able to swallow. Depression and suicide are very common with people suffering from the disease. As the disease progresses, the person will need assistance and may even eventually need 24-hour health care. Therapies that are being tested on animal models have to this date shown benefits for the health of humans and possibly find a cure. The ideal method of the gene therapy has been debated and viral vectors have provided one method of long term and wide spread delivery to the