Huntington’s disease is a progressive neurological disorder that alters your physical movement, thinking abilities and mental health. Symptoms of Huntington’s disease include:
- Cognitive decline (dementia)
- Involuntary movements (chorea)
- Walking abnormalities with falls
- Mental symptoms such as depression, anxiety and psychosis
Huntington’s disease typically occurs between the ages of 30 and 50 years. Occasionally, children and elderly adults receive a Huntington’s disease diagnosis. Mental and physical abilities decline over five to 20 years. Without a cure, this disease is fatal.
A gene mutation causes Huntington’s disease. You inherit the mutated gene from one parent. This means if you have a parent with Huntington’s disease, you have a 50% chance of getting the disease. Siblings and parents of a person with the condition also have a 50% chance of inheriting it.
Our Movement Disorders Center can help you cope with some of the physical, mental and emotional symptoms as the condition progresses.