We have research studies for individuals with Huntington's disease. To find out more, please complete the contact form, and our recruitment team will be in touch.
Huntington’s disease is a progressive nervous system disorder that is caused by mutations in the HTT gene, which leads to an increase of CAG repeats in the huntingtin gene. It is an autosomal dominant disorder, which means that each child of an affected parent has a 50% chance of developing the disorder.
The most common symptoms are: