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Huntingtons disease autosomal or sex linked

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    Huntington disease is a progressive brain disorder that causes uncontrolled movements, emotional problems, and loss of thinking ability cognition. Adult-onset Huntington disease, the most common form of this disorder, usually appears in a person's thirties or forties. Early signs and symptoms can include irritability, depression , small involuntary movements, poor coordination, and trouble learning new information or making decisions. Many people with Huntington disease develop involuntary jerking or twitching movements known as chorea. As the disease progresses, these movements become more pronounced.
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    Huntington disease

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    Huntington's disease - Symptoms and causes - Mayo Clinic

    When a certain gene is known to cause a disease, we refer to it as a single gene disorder or a Mendelian disorder. For example, you may have heard of cystic fibrosis, sickle cell disease, Fragile X syndrome, muscular dystrophy, or Huntington disease. These are all examples of single gene disorders. As a rule, single gene disorders are not very common. For example, only one in 2, people are born with cystic fibrosis. There are a number of inheritance patterns of single gene disorders that are predictable when you know what they are. Autosomal dominant means that a person only needs one copy of the changed gene genetic difference in order to have the disorder.
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    Huntington's disease

    Huntington's disease HD , also known as Huntington's chorea , is a neurodegenerative disease that is mostly inherited. HD is typically inherited from an affected parent , who carries a mutation in the huntingtin gene HTT. No cure for HD is known, and full-time care is required in the later stages.
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    Gender plays a role in the prevalence and natural course of several disorders. It is apparent in neurodegenerative diseases like Parkinson's disease more prevalent in men, Alzheimer's disease more prevalent in women, or Lewy body dementia more prevalent in men. Rarely, however, recently more often, in autosomally conditioned diseases, gender differences are being identified 1 — Huntington's disease HD as a rare neurodegenerative recently reported peripheral tissue involvement , incurable—therefore still displaying natural course—disorder with an autosomal dominant pattern of inheritance with full penetrance in most cases
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