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An inherited condition in which nerve cells in the brain break down over time.

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Here is what Huntington's Disease looks like.

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Who discovered Huntington's Disease? Where?

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Who discovered Huntington's Disease? Where?

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George Huntington discovered "Huntington's Disease" in East Hampton, Long Island in 1872.

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George Huntington was an American physician who contributed a classic clinical description of the disease that bears his name – Huntington's disease.

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Huntington's Disease affect the brain with uncontrollable movement and thinking.

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How Does Huntington's Disease affect your life/Lifespan?

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How Does Huntington's Disease affect your life/Lifespan?

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People do not die from Huntington's disease, but people that do have Huntington's Disease don't think like normal people.

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A picture showing the genes of someone who has Huntington's Disease.

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What Chromosome carries Huntington's Disease?

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What Chromosome carries Huntington's Disease?

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The chromosome that carries Huntington's Disease is chromosome 4, carrying a defective gene.

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Are There any Treatments for Huntington's Disease.

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Are There any Treatments for Huntington's Disease.

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There are two forms of treatments for Huntington's Disease. The first treatment being therapy, physical and counseling.The second is having a specialist, like a neurologist, psychiatrist, primary care provider, or medical geneticist.

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Huntington's Disease usually develops between ages 30 and 50, but could occur as early as age 2 and as late as age 80.

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Here is a video that explains Huntington's Disease.

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Huntington disease - causes, symptoms, diagnosis, treatment & pathology

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What is Huntington disease? Huntington disease is a type of autosomal dominant disorder involving a triplet repeat of CAG, leading to an abnormal protein that results in neuronal cell death, and various movement and cognitive-related symptoms. Subscribe - https://goo.gl/w5aaaV. More videos - https://goo.gl/UhOKiM. Support us on Patreon - https://goo.gl/ZGHEk4.