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Huntington's Disease

Huntington’s disease is a hereditary disorder that destroys certain areas of the brain involved in intellect, emotion, and movement development. It is characterized by the loss of mental abilities; developing of emotional problems; and uncontrollable movement of the limbs and face.

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Does Huntington's disease affect a specific population of people?

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Since it is a genetic disease, it only affects people who have at least one parent that had Huntington's. Those people can be any race or sex. It is more common among people with an ancestor from England, since that is where the disease began.

What does huntington's do to the body?

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huntingtons damage it the muscles.....Jason es burgers.

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What race is huntington's disease most common in?

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In Western countries it is estimated that 5 to 7 people per 100,000 have Huntington's disease. There are a few isolated populations in Western Europe where HD is unusually common. Please see the related link below.

Differences of cystic fibrosis and huntington's disease?

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Cystic fibrosis is where your lungs and digestive system get clogged up with mucus and you get the effects from birth. People often die from lung complications and lack of nutrients. whereas Huntington's disease effects your muscle coordination and some cognitive functions. The effects generally come out at middle age but can come out before.

Did Woody Guthrie had Huntington's Disease?

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Yes, Woody Guthrie died from complications of Huntington's Disease.

What is the physical appearance of a person with Huntington's Disease?

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Until the physical symptoms become apparent, they will look like anyone else. When symptoms DO become apparent, you might think the person is intoxicated. Clumsy, unsteady walk, jerky movements, slurred speech.

What are the short term effect from the Huntington disease?

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Properly known as Huntington's Disease, it is a fatal genetically transmitted condition that causes deterioration of the central nervous system, including changes in the structure of the nerve cells in the brain (known as spiky neurons). The symptoms are gradual worsening of muscle control, both voluntary and involuntary. Persons may have trouble walking without staggering, lose their balance, stumble, have slurred speech. Impaired ability to swallow is common. The disease also has an emotional component- personality changes that include rapid severe mood swings, irrational angry outbursts, etc. For more information, please visit the website for the Huntington's Disease Society of America.

What are the social effects of huntingtons disease?

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The effects of HD on personality can have a significant impact. Those can include depression, sharp mood swings, and irrational angry outbursts. A person with HD may be mistaken for an intoxicated person- unsteady walk, slurred speech, poor balance.

Who has done research on huntington's disease?

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Yep. Go to the website for the Huntington's Disease Society of America for more information.

What are the contraindications to massage in Huntington's disease?

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what kind of massage should a huntington diseased person recieve

How does genetics control characteristics for Huntington's Disease?

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There is really only one risk of developing Huntington's Disease- that one of your parents had it. It is a genetically transmitted disease- you inherit it. There is no way to catch HD, or behaviors that make you more likely to get it.

What allele and chromosome is huntington's disease found on?

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The gene codes for a protein called huntingtin found on the short arm of chromosome 4.

Is Huntington's Disease a gene mutation?

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No, it's caused by a single point mutation of a gene.

Punnett square examples for Huntington's disease?

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You could use a Punett Square for Huntington's disease, but why bother? If one parent has the disease, there is a 50% chance that a child will get it. The other factor involved is that with gene therapy advancing so fast, it is possible that it will be possible to replace a single gene in a particular chromosome in a baby born today before that baby reaches 30 years of age. Since Huntington's disease involves one gene on one chromosome, it should not be much of a problem.

Is huntingtons disease a autosomal ressesive trait?

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Huntington's Disease is an Autosomal Dominant Trait, meaning that only one parent needs to pass the disease for the offspring to inherit it.

Is huntington disease dominant or trait?

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There is two answers, it is autosomal dominant showing incomplete dominace

How many births are affected with huntington's disease?

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World wide around 8 cases per 100,000 persons are affected by Huntington's Disease. The number varies somewhat because it is genetic.

What are true statements about Huntington's Disease?

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In the United States, about 1 in every 30,000 people has Huntington's Disease.

Is there are cure for huntingtons disease?

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No, there is currently no cure for Huntingtons, but a neurologist is able to prescribe medication to patients with Huntingtons to help the suppress the symptoms. Researchers are currently looking into stem cell research for a cure.

What specific groups does huntington's disease affect?

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Huntington's disease is a dominant genetic disease. That means that a person will develop the disorder if they receive one copy of the gene from an affected parent - so children with a parent who has Huntington's have a 50% chance of inheriting the gene and developing the disease. If children don't inherit the gene, however; they cannot pass it on to their own children. The chain of inheritance is broken.

Huntington's disease typically doesn't appear until the patient is between 30 and 50 years of age. Men and women are equally affected by the disease, and it crosses all racial and ethnic boundaries.

Can 2 people with Huntington's Disease produce an offspring who does not have Huntington's disease?

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Unfortunately, no. Huntington's is carried on a dominant gene. One parent HD, one non-HD, you have a 50-50 chance of not inheriting that gene. But two parents that are HD, you will inherit the gene from one parent or the other.

Can you live if you have huntingtons disease?

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Yes, Huntington's disease (know as HD) is a fatal neurological disease. HD is generally fatal within 20 years of symptoms first appearing. At this time (2011-03-20), there is no way to reverse or stop the course of HD, but research continues. In recent years, scientists have made a number of breakthroughs in this area. The future may well bring a cure.