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If the disease develops before age 20, it's called juvenile huntington's disease Huntington’s disease impacts areas of the brain that affect things like movement, behavior, and communication 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.
Symptoms typically appear in adulthood, often between the ages of 30 and 50, though they can vary widely.
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