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Learn about the early signs of huntington's disease, how health providers diagnose and treat huntington's disease, and how common the disorder is. Symptoms typically appear in adulthood, often between the ages of 30 and 50, though they can vary widely. Huntington's disease symptoms can develop at any time, but they often begin when people are in their 30s or 40s
If the disease develops before age 20, it's called juvenile huntington's disease Early signs of the disease may include changes in mood, trouble concentrating, and clumsiness. When huntington's develops early, symptoms can be different and the disease may have a faster progression.
Huntington’s disease is a rare, inherited neurological disorder that progressively impacts the brain, affecting various aspects of life.
Huntington’s disease is a progressive neurodegenerative disease that develops over several decades The first signs of huntington’s disease are often subtle changes in coordination, such as clumsiness or trouble with balance You may also begin to notice changes in thinking, such as difficulty. The first signs of huntington's disease often appear when people are in their 30s or 40s and may include clumsiness, stumbling, or difficulty focusing.
Huntington’s disease is a progressive brain condition that affects your brain cells Learn more about the symptoms, available treatment and prognosis. What are the first signs of huntington’s disease Discover the first signs of huntington's disease and how early symptoms affect behavior, movement, and cognition.
Huntington’s disease impacts areas of the brain that affect things like movement, behavior, and communication
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