Description Of Huntington's Disease

Improved Essays
Thorough description of the disorder
Huntington’s disease is a genetic disorder that affects muscle coordination and leads to mental decline and behavioral symptoms. It breaks down nerve cells in the brain called neurons. Neurons are specially designed to transmit information. When neurons break down, the body can’t control all of its movements. The brain controls the entire body and when the nerves in the brain break down, it causes your body to glitch. This is why a person with this disease experiences muscle twitches and can’t control all of their movements. Huntington’s is caused by a mutation in the gene for a protein called Huntingtin. This is why the neurons break down.
Huntington’s disease is passed on by family members. Someone can
…show more content…
It is not a sex or race specific disease, but it is more common in the white population. It affects about 1 in 10,000 Americans. (http://patient.info/health/huntingtons-disease-leaflet)

Modes of inheritance
Huntington’s disease is passed on from parents to child. Each child with a parent who has the disease has a 50 percent chance of inheriting the disease. If an individual does not have the disease they cannot pass it on to anyone else. Someone can only inherit the disease if one of their parents has the disease.
(http://www.medicinenet.com/huntington_disease/page2.htm)

Symptoms
Huntington's disease causes psychiatric, movement and thinking problems. Some movement problems include chorea (involuntary jerking or twitching), dystonia (muscle problems), abnormal eye function, bad posture and balance, and problems with swallowing and eating. There are also cognitive problems that include: difficulties learning new, difficulties organizing and focusing on task, not being able to process thoughts very well, and no flexibility in a schedule. Because of all the other systems of Huntington’s, psychiatric problems can also show. These problems can include: feelings of sadness, social withdrawal, loss of energy, suicidal thoughts or death.

Related Documents

  • Great Essays

    Some patients have a genetic predisposition to developing the disease. Other…

    • 1447 Words
    • 6 Pages
    Great Essays
  • Decent Essays

    This disease is caused by a mutation on chromosome 14 the GALC gene. The CALC gene is responsible for the production of an enzyme called galactosylceramidase. When there is a deficiency in the galactosylceraidase it causes the destruction of the myelin of the nerve cells in the brain and nervous system. The myelin protects and insulates the nerve to send signals to different parts of the body.…

    • 112 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Although it is a rare disease, it is easier to inherit because only one parent is needed to inherit and not…

    • 1033 Words
    • 5 Pages
    Improved Essays
  • Great Essays

    Research Paper On ALS

    • 2288 Words
    • 10 Pages

    Amyotrophic lateral sclerosis affects the nerve cells in the brain and spinal cord. These nerve cells are called motor neurons. This disease is neurodegenerative- meaning that the motor neurons are “degenerated”, meaning they become weak, in this case,…

    • 2288 Words
    • 10 Pages
    Great Essays
  • Superior Essays

    The motor neurons serve as the body’s way to communicate. Upper motor neurons in the brain send messages to the lower motor neurons in the spinal cord. In Amyotrophic Lateral Sclerosis the neurons die or degenerate, which stops communication to the voluntary muscles. As the neurons stop sending messages to the muscles, the muscles gradually waste away, this is known as atrophy. Eventually all voluntary muscles lose the ability to move.…

    • 930 Words
    • 4 Pages
    Superior Essays
  • Improved Essays

    Dementia is an umbrella term. By this I mean that it covers many different conditions. Each condition affects the brain and can lead to dementia due to brain de deterioration and loss of function. Wernicke-Korsakoff syndrome- this is a brain disorder in which not getting enough B1 vitamin will affect your brain function. B1 vitamin is used in the brain to change sugar into energy.…

    • 356 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Tay-Sachs's Disease

    • 697 Words
    • 3 Pages

    A kid can get the gene passed down to them but not necessarily have the disease. If both the parents carry the gene, then one in four children will actually have the disease. If the parents have four kids, one will have the disease, one will carry it and the other two children will have no remains…

    • 697 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Mothers who are carriers of the gene may pass the gene to the offspring. In males, the gene will be expressed, and females would become carries, due to the fact that most females do not show any signs or symptoms of Duchenne’s. Statistics about Duchenne’s in the United States In the United States, the defective gene dystrophin that effects proteins and is found to cause Duchenne’s muscular dystrophy, is present in 1 out of every 3,600 male infants.…

    • 1182 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Huntington's Case

    • 720 Words
    • 3 Pages

    Meghan was two when her father was diagnosed with Huntington's. At the time, she didn't understand what that was. In 2006, in College, while pouring herself some lemonade, she spilled the pitcher and knocked her glass on the floor. When her mother was helping her clean up the mess, Meghan told her she thought she had Huntington's disease. Her mother has seen the symptoms for a few years, and she finally told her that she knew.…

    • 720 Words
    • 3 Pages
    Improved Essays
  • Great Essays

    Genetics is random, for an example, if the mom or dad has it, the children will have a fifty fifty chance of getting it, but things will be different if the disorder alleles is dominant. According to the table of Huffman and Sanderson (2014), “Relationship to person with…

    • 1534 Words
    • 7 Pages
    Great Essays
  • Great Essays

    The brain is the most important body organ in your body nothing can function without your brain. The brain contains the way it moves, feels, and its senses of emotions, including the lungs, heart, and stomach. which is the part to the central nervous system. There are three main structures of the brain, the forebrain, midbrain, and hindbrain. Forbrain their are two different types of forebrain which is (diencephalon and telencephalon).…

    • 1094 Words
    • 5 Pages
    Great Essays
  • Improved Essays

    Papers On Dementia

    • 594 Words
    • 3 Pages

    Huntington’s disease most common in older adults is an inherited disease which can cause certain types of brain cells that control movement as well as thinking. These damage brains cells in both cortical and subcortical areas ("Dementia Causes, Symptoms, Treatment - Dementia: Irreversible Causes - eMedicineHealth," n.d., page…

    • 594 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    My diseases are Huntington’s disease and gouty arthritis. If someone in your family has Huntington's disease it's a great chance you have that disease. Huntington's disease is a rare genetic disease that hits in your middle ages, that's why it's good to know the signs, symptoms, treatments, preventions , and background information. Agonizing pain in your big toe is one of the leading signs of gouty arthritis or gout. If you're a male and after the age of 30 you should know the signs, symptoms, treatments, preventions, and background information so it won't happen to you.…

    • 825 Words
    • 4 Pages
    Superior Essays
  • Improved Essays

    A family history has many factors in common that play a critical role in genetic disorders. Understanding fully the hereditary contributions of the illness can help the family identify their potential risk factors of inheriting the disease (Kaakinen, Coehlo, Steele, Tabacco, Hanson, & Rowe, 2014). Throughout this paper I will discuss a genetic disease passed down through a three generation family, discussing the family’s health problems, ethnic history, their understanding of the disease and providing nursing interventions to help this family reduce their genetic health risk. The three generation family I choose to write about are all males, a grandfather ninety-seven, a son seventy-six and a grandson fifty-two years old.…

    • 749 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Parkinson’s Disease: It is a genetic disorder that affects the central nervous system. This diseases’ common symptom is stiffness in the the body. People may experience trouble walking and moving. It often starts with tremors. It can also affect the voice and the eyesight.…

    • 609 Words
    • 3 Pages
    Improved Essays