The Alzheimer’s Association defines Huntington’s disease as “a progressive brain disorder caused by a defective gene.” It is an inherited condition (meaning that the disorder may run in families) that slowly degenerates nerve cells in the central area of the brain that are responsible for movement, mood, and cognitive function.
While most people with Huntington’s disease develop signs and symptoms in their 30s or 40s, it’s possible for it to develop much earlier or later in a person’s life. The following are six early warning symptoms to be mindful of, especially if the disorder runs in your family.
Poor Coordination
At the onset of the Huntington’s disease, coordination issues may be so slight that they are easily dismissed. These changes may include compromised balance, clumsiness, stumbling while walking, or slight difficulty with daily activities (such as driving).
As the disease progresses, however, these symptoms will worsen. Eating can also become a problem in later stages, as diminished coordination may cause a person to spill or drop food.