Muscular Dystrophy Research

Improved Essays
It had been determined that specific types of Muscular Dystrophy only affect men. For instance the Duchenne is most commonly known for affecting young children, but Duchenne muscular dystrophy is also know to only affect makes. This type of condition and reductions the muscle in mass and causes it to diminish and become weaker and weaker. This disorder is know to have significant affects on young boy, and by the age of 12 they will require the use of a wheel hair. With time the limbs and spin will become considerably mutilated and there by become compromised. Most males diagnosed with this disorder will not live past the age of 30. Additionally, Becker a form of Muscular Dystrophy only affects males, but is much minor for the symptoms do not …show more content…
The ages being most affected are early on, from zero to 40 being the greatest diagnosed and then decreasing number of individuals from there (Mayo Clinic Staff, 2014). Research conducted by the Centers for Disease Control and Prevention shared the “Prevalence of Duchenne/Becker Muscular Dystrophy Among Males Aged 5-24 Years- Four states, 2007” collected, it concluded that 1 in evert 7,250 mailed from the ages of five to 24 years old had an exceeded predominance of Duchenne and Beck muscular dystrophy. It was analyzed that the occurrence of DBMD was greater in Hispanic and Non-Hispanic white individuals than in Non-Hispanic blacks. Additionally, the prevalence of Becker muscle dystrophy was three times less than the popularity of Duchenne muscular dystrophy. It was determined that the average age that a person is typically diagnosed is between 5 years of age. Since the disease is known to alter the ability to walk, many of those diagnosed up end up using a wheel chair. It was shared that 90% (9 in 10) of males will report to using a wheel chair from the aged of 15 to 24, 82% (8 in 10) will be in a wheel chair by the age of 14, and the disability will not be severe enough from the child to be in a chair from the ages 5 to nine with only 29%, 3 in of 10 of males using a wheel chair during that age. Because the disease can …show more content…
The disease is said to affect people very early on in life, and most often then not will end up taking ones ability to walk, restraining their moment to a wheel chair, or worse, the total take over of all limbs. Since there is no sight of a cure so far, people resort to physical therapy, daily exercise, and for some in highly need will use medications such as steroids. For now this is the most that can be done to help improve the quality of life for individuals diagnosed or born into Muscular Dystrophy. It is important to note that not all persons suffer incredibly, some do have the ability to carry on daily life task and live unaffected, but through this it is important to know if the mutation gene is carried and has the potential to be given off to ones future offspring. A cure is sure to come in the future, and when it comes it will improves greatly the lives of many people living with the disease and can thus completely improve the quality of life for the affected and their

Related Documents

  • Improved Essays

    Adrenzo Movie Analysis

    • 613 Words
    • 3 Pages

    Most of which are portrayed in the film. Adrenoleukodystrophy is passed down from the parents to their children as an X-linked genetic trait. Therefore, it affects mostly males, although some women who are carriers can have milder forms of the disease. Treatment for ALD is simple, Lorenzo's oil can help give the body the longer chain of fatty acids. This treatment is being tested for X-linked adrenoleukodystrophy, but it does not cure the disease and may not help all patients.…

    • 613 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Duchenne muscular dystrophy (DMD), the most common form of all muscular dystrophies, is an X-linked disorder affecting approximately one in 5000 newborn boys. " (page1; paragraph 1; lines 1-4)" Patients are usually restricted to a wheelchair around the age of twelve and facing death somewhere between the ages twenty-five to thirty. DMD is caused when the dystrophin gene is mutated. That mutation stops the communication for a functional protein.…

    • 533 Words
    • 3 Pages
    Improved Essays
  • Decent Essays

    In people with MD, though, these genes have wrong information or leave out important information, so the body can't make these proteins properly. Most kids with MD have Duchenne MD. Kids with Duchenne MD look and act just like other kids when they're babies. But when they're between 2 and 6 years old, the muscles in their arms, legs, and pelvis (hips) begin to get weaker. The first signs of weakness might be trouble with running, going up the stairs, or getting up off of the floor.…

    • 116 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Many children with this disease will end up in a wheel-chair and will eventually need assistance to move their arms and legs (Signs and Symptoms n.d.). This disease can also cause the weakening of the heart which can lead to a condition that is called cardiomyopathy (Signs and Symptoms n.d.). During the pre-teen years the diaphragm that helps operate the lungs can be affect resulting in less effective lungs (Signs and Symptoms n.d.). Duchenne muscular dystrophies on average affects 1 in 3,500 to 5,000 newborn male’s worldwide (Duchenne and Becker…

    • 372 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    From showing pigs to playing football, Teagan Imler was a very active little boy up until he was fitted for a wheelchair at the age of 10. In 2013 a family from Everett, Pennsylvania found out that it was very likely that their little boy had a lethal disease called Duchenne Muscular Dystrophy (DMD). This is a disorder that is characterized by progressive muscle degeneration, and it is often found in males during childhood. Teagan was diagnosed with DMD at the age of 6. They started noticing differences in things that their younger son, Josten, was able to do that Teagan never did, so they asked the pediatrician at Teagan’s 6 year check up.…

    • 994 Words
    • 4 Pages
    Improved Essays
  • Great Essays

    160116 Duchenne Muscular Dystrophy “Muscular dystrophy (MD) is a genetic disease characterized by progressive weakness and degeneration of the skeletal or voluntary muscles which control movement” (Muscular dystrophy, 2013). Muscular dystrophy is classified into nine major types that each affect specific muscle groups, certain age groups and are identified by different signals. Duchenne muscular dystrophy most commonly affects males and is targeted at younger children (Facts about Muscular Dystrophy, 2015). “The Centers for Disease Control and Prevention estimated that 1 out every 5,600 to 7,700 males between the age of 5-24 has DMD” (Seiner, Duchenne Muscular Dystrophy).…

    • 1194 Words
    • 5 Pages
    Great Essays
  • Improved Essays

    MDA Research Paper

    • 467 Words
    • 2 Pages

    MD is a disease that weakens your muscles and stops you from doing more things. I believe that scientists should work on finding a cure or do something to help for people with MD. If you help donate to Muscular Dystrophy Association you could help make more medicine to help people with MD. I will be talking about how MDA has events, about the association and what MD is. MDA holds a lot of events such as 5k walks/runs to help raise money for the people suffering this disease.…

    • 467 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Muscular Dystrophy Muscular Dystrophy is a group of disorders characterized by a progressive loss of muscle mass and consequent loss of strength. There are multiple types of muscular dystrophy, each type affecting a different part of the body. Examples would be Duchenne muscular dystrophy, which effects toddlers starting from their third birthday and causing them to be in a wheel chair by the time they are 12 and usually dying from respiratory failure in their late twenties, early thirties. Becker muscular dystrophy is similar to Duchenne, it just starts later on in life and has a slower attack, most die in their mid forties.…

    • 530 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Duchenne MD

    • 1444 Words
    • 6 Pages

    A short timeline is provided in the book Muscular Dystrophy; it provides information to describe readers the symptoms that begin to show at different ages. Around nine years old, the child is unable to stand from a sitting position. At the age of ten years old, the child shows loss of ability in standing from ground level, climbing stairs, and he or she is beginning to walk only with the help of support braces. At 11 years of age, children with Duchenne muscular dystrophy cannot usually walk for even thirty minutes at a time, and this worsens by age 12, when a wheelchair is often required full time (Muscular p.…

    • 1444 Words
    • 6 Pages
    Superior Essays
  • Decent Essays

    Muscular Dystrophy affects your muscle by making it get smaller and smaller by the hour until nothingness and you can't move at all and you basicly dead without help from other people. How this affects your life-say you have a wife and you want to go some where and you are at the top of the staris your wife has to come and get you and bring you dwon the staris on her back.…

    • 73 Words
    • 1 Pages
    Decent Essays
  • Decent Essays

    Abstract on the muscular system and muscular dystrophy: Muscular dystrophy is weakening of the muscle and can be passed down but most of the time it is not. Muscular dystrophy does not only affect our muscle but it can affect the way we breathe. When the diaphragm has been damaged our abdominal muscles provide support for breathing because one uses their diaphragm most of the time. Also if the diaphragm is not doing its job then the abdominal muscles will not work either. Also in muscular dystrophy ones balance can be difficult to keep the same meaning it changes if the diaphragm is not working.…

    • 196 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Mutations in the DMD gene, which creates dystrophin, causes Muscular dystrophy. Dystrophin is located in the skeletal and and cardiac muscles. Alterations or mutations in the gene make it so little to know dystrophin are produced, causing Muscular Dystrophy. Without enough dystrophin muscles contract and get damaged. (2015)…

    • 341 Words
    • 2 Pages
    Improved Essays
  • Superior Essays

    Once the child is born, if they have Duchenne’s, there are ways that the genetics counselor can be used to assist in treatments, such as the myoblast injections. Conclusion What I’ve learned about Duchenne’s muscular dystrophy is that it is a disease of the muscles that ultimately leads to a shortened life of every 1/3,600 males. In addition to the muscles being targeted, I learned that death does not just occur from being confined to a wheelchair and having atrophied muscles, the respiratory system eventually shuts down from the lack of muscle in the heart at diaphragm and that is why death occurs.…

    • 1182 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Muscular Dystrophy Essay

    • 1251 Words
    • 5 Pages

    Occurring mostly in males, Duchenne Muscular Dystrophy is an X-linked disorder that includes progressive muscle weakening caused by an insufficient gene for the production of a protein in the muscles called dystrophin. (Lucas-Heron, 1995) It affects about one in 3600-6000 live male births, making it the most common form of muscular dystrophy. Symptoms are most often noticeable by the time patients reach the age of three to five. The affected males will lose their ability to walk by eight to twelve years of age, making them wheelchair dependent.…

    • 1251 Words
    • 5 Pages
    Improved Essays
  • Great Essays

    Sarcopenia Case Studies

    • 2330 Words
    • 10 Pages

    AIM: Sarcopenia has been defined as an involuntary loss of skeletal muscle mass and strength and/or function. The presence of sarcopenia in patients with Parkinson’s disease (PD) may have prognostic effects and may be mistaken for poor therapeutic control of PD. We aimed to evaluate sarcopenia in patients with PD.…

    • 2330 Words
    • 10 Pages
    Great Essays