Preview

Muscular Dystrophy

Good Essays
Open Document
Open Document
1750 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Muscular Dystrophy
The combination of growing progressively weaker, losing the ability to walk, and dying at an early age may be due to Muscular Dystrophy, also called (MD). Muscular dystrophy is a genetic mishap that weakens the body's muscles. There is no single disease called muscular dystrophy. Muscular Dystrophy refers to a group of more than 30 inherited diseases. These diseases affect the voluntary or skeletal muscles, which control the movements of legs, arms, and other limbs. Some organs, such as the heart and the gut, are also affected by the disease. Muscular Dystrophy can prevent the movement of the muscles any human who carries the trait, and varies depending on the type.
It Can Affect Anyone
Every form of muscular dystrophy is inherited; it is associated
…show more content…

Although some muscular dystrophies cause muscle problems in children, as stated above, other victims’ symptoms do not present themselves until adulthood (Clark1). One of the most common forms of Muscular Dystrophy in adults is Myotonic Muscular Dystrophy. It affects both men and women, and it usually appears any time from early childhood to adulthood (Hirsch1). It is extremely rare for newborns to suffer from Myotonic Muscular Dystrophy. The name refers to a symptom, myotonia spasm, meaning stiffening of the muscles after use. There are nine total major forms of muscular dystrophy: Myotonic, Duchenne, Becker, Limb-girdle, Facioscapulohumeral, Congenital, Oculopharyngeal, Distal and Emery-Dreifuss (Clark1). Duchenne Muscular Dystrophy symptoms appear early in life, often between the ages of 1 and 6. The condition advances rapidly. Many people result to needing a wheelchair by the age of 12. Symptoms include those previously listed, plus fatigue and bone problems in the back and chest. Individuals with the condition may eventually have trouble breathing and develop pneumonia. They may also sometimes grow to be mentally impaired. Becker's Muscular Dystrophy, which usually begins around age 12, is much less austere than Duchenne Muscular Dystrophy. The symptoms include those previously listed, in addition to heart disease, problems with the curvature of the spine, fatigue, …show more content…

Consistent pain from Muscular Dystrophy is categorized by tenderness, soreness and in some cases inflammation. This disorder affects people of all ages (Bagasis, 2011). Because the disease affects joints it is hard for those with Muscular Dystrophy to maintain healthy functioning. Muscular Dystrophy can occur at different stages of a person's life, from an infant to middle age or even later in life (Kumar, 2011). A child diagnosed with Muscular Dystrophy gradually loses the ability to do things such as walk, sit upright, breathe easily, and move the arms and hands (Sokka, 2012). This disorder also affects both

You May Also Find These Documents Helpful

  • Powerful Essays

    Anatomy Case paper

    • 2241 Words
    • 9 Pages

    Muscular Dystrophy: is a group of inherited disorders that involve muscle weakness and muscle loss gradually decline over a period of time.…

    • 2241 Words
    • 9 Pages
    Powerful Essays
  • Good Essays

    Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.…

    • 1511 Words
    • 6 Pages
    Good Essays
  • Better Essays

    Dystonia can affect many or single muscle groups in the body, also meaning that the symptoms can range from quite severe to minimal depending on the extent of the disorder. Dystonia is not limited to one gender and can present itself at any age. Although there are many forms of Dystonia , the disorder can be (generally) categorized into two immediate groups, primary and secondary Dystonia. Primary Dystonia is seen as a genetically based type of Dystonia and is most commonly found in children. Although primary Dystonia can be a debilitating disease, it does not usually affect the non-movement related functions of the brain meaning that the person who has the disorder would be able to comprehend their situation but not physically express themselves or live to a normal capacity in worst case scenarios. In the primary Dystonia group also resides another branch called late-onset or adult-onset primary Dystonia that is developed over the age of 30; it is presumed to be a hereditary disorder and is less common. The other type (group) of Dystonia is called secondary Dystonia. Secondary Dystonia is usually the result of injury, pressure or trauma to the brain but it can also be an unseen result of illness or disease .…

    • 1371 Words
    • 6 Pages
    Better Essays
  • Good Essays

    What is Duchenne Muscular Dystrophy and where does it come from? Firstly, it is a kind of muscle dystrophy. The word dystrophy refers to when an organ or tissue wastes away. A muscle dystrophy is a group of many inherited disorders that cause loss of muscle tissue and weakness in muscles. Duchenne Muscular Dystrophy is a genetic disorder characterized by progressive muscle degeneration and weakness caused by a defective gene for dystrophin, a protein in the muscles, and founded by French neurologist Guillaume Benjamin Amand Duchenne in the late 19th century.…

    • 884 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Spinal muscular atrophy [SMA] is a disorder in which, you have a loss of motor neurons. Your muscle symmetry is often off. In addition, there is muscle weakness in your spinal cord. This occurs in a hard time sitting up and holding your head up on your own. It is just like when you are a newborn and you need a pillow to sit on the couch. A few major causes of SMA are loss of motor neuron cells or nerve cell. This mutation leads to a deficiency of motor neuron cells or nerve cells. The disorder SMA is tied to the gene "SMN1" and tied to chromosome 5. A few symptoms of this disorder are- difficulty breathing lack of oxygen, difficulty eating, floppy posture, small amount of movement, and all these symptoms will gradually get worse over time. All these symptoms are at about a mild level in the beginning.…

    • 417 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Duchenne muscular dystrophy is a muscular dystrophy but in order to understand it and how it works you will need to know about genetics and how they work and after that, I can tell you about a few treatments and therapies.…

    • 1325 Words
    • 6 Pages
    Good Essays
  • Satisfactory Essays

    Duchenne muscular dystrophy (DMD) is a rare genetic disorder characterized by progressive muscle degeneration and weakness. DMD is caused by a mutation of a gene on the X chromosome that causes an absence of dystrophin, a protein that helps keep muscle cells intact. This very rare disease primarily affects young boys. Its symptoms include muscle weakness which can begin as early as the age of 3, first affecting the voluntary muscles such as the hips, pelvic area, thighs and shoulders, and by the early teens the involuntary muscles are affected such as the heart and lungs. There is no cure for this disorder. Boys affected by DMD did not survive beyond their teenage years until recently. Due to advances in cardiac and respiratory care, life…

    • 149 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Duchenne Muscular Dystrophy is caused by the lack of a protein called dystrophin and is fatal with the further developed symptoms. Without dystrophin the muscles expand, which makes it difficult to walk, sit, climb, stand, jump, and run. That is, the body makes no dystrophin for the muscles to be normal, and consequently a…

    • 1141 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Lou Gehrigs Disease

    • 868 Words
    • 3 Pages

    Amyotrophic lateral sclerosis; Motor neuron disorders are far from rare: Parkinson’s disease, multiple sclerosis, and a variety of lesser diseases all come under that heading. A disease of the nerve cells in the brain and spinal cord that controls voluntary muscle movement. ALS, Lou Gehrig’s disease, Amyotrophic lateral sclerosis are all names for this horrid disease. The symptoms; Difficulty breathing, sudden paralysis. Treatment is slim to none but there are known medications to help subside the pain that may be felt. The Cause is unknown, doctors are unsure if this disease is genetic or cause by one’s self.…

    • 868 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Because patients with muscular dystrophy are especially susceptible to muscle damage, Physical Therapists, who are skilled in the involvement of skeletal muscle and the effects that skeletal muscle has on joints, are Ideal clinicians to care for patients with muscular dystrophy. 2 Physical therapy is most successful when it is began as soon as possible, preferably right after receiving a diagnosis. This way the physical therapist can teach skills and begin interventions before severe joint tightness, muscle tightness, or contractures develop. 1,2 “Light to moderate exercise has been shown to be benefit patients with muscular dystrophy by slowing down the progression of muscle weakness”, however “Over exercising can damage muscles.” 1,2 Maximal…

    • 483 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Muscular Atrophy is a decrease in the mass of a muscle. This leads to muscle weakness. An 84-year old thin white female with this disease will be in constant discomfort and is already lacking in muscle because of her age and size and will become weak due to the decrease of muscle mass. She will be unable to perform certain tasks or worsen the risks of accidents while performing normal daily activities such as walking. This disease is common among the elderly. (Wikipedia,…

    • 302 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    Muscular dystrophy (MD) is a term that applies to a group of hereditary muscle-destroying disorders. According to the Muscular Dystrophy Association, in 2006 some type of MD affected approximately one million Americans. Each type of the disease is caused by defects in the genes that play important roles in the growth and development of muscles. In MD the proteins produced by the faulty genes are abnormal, causing the muscles to slowly disintegrate. Unable to function properly, the muscle cells die and are replaced by fat and connective tissue. The symptoms of MD may not be noticed until as much as 50% of the muscle tissue has been affected. All of the different types of MD cause weakening and wasting of muscle tissues. They vary, however, in the usual age at the beginning of symptoms, rate of progression, and initial group of muscles affected. The most common childhood type, Duchenne Muscular Dystrophy, affects young boys, who show symptoms in early childhood and usually die from respiratory weakness or damage to the heart before becoming an adult. The gene is passed from the mother to her children. Females who inherit the defective gene generally do not have symptoms, they simply become carriers of the defective genes, and their children have a 50% chance of inheriting the disease. Other forms of MD become apparent later in life and are usually not fatal.…

    • 302 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    As you may know, Muscular Dystrophy is a disorder that weakens a person's muscle. More than 50,000 people are diagnosed with that kind of disorder. They usually come from the…

    • 552 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Spinal Muscular Atrophy also known as SMA is a genetic disease affecting the part of the nervous system that controls the voluntary muscle movement. It can be passed down from parent to child. The major causes of SMA is a deficiency of a motor neuron protein called SMN. Mutation in the survival motor neuron gene 1. The symptoms of SMA are very sad a child is weak and has a delay in meeting feeding and breathing development milestones. There are four types of SMA, type 0 is the most severe it can happen to a child inside the mother and grow worse when their born. Type 1 is severe but not as severe as type 0 it can be present at the birth of the child. Type 2 is milder but still bad it contains muscle weakness. Type 3 is not bad at all but still…

    • 365 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Muscular Dystrophy

    • 306 Words
    • 2 Pages

    Muscular Dystrophy is a general term for a number of hereditary, degenerative disorders affecting skeletal muscles, and often other organs. It is a genetic disease that causes constant degeneration of the muscles. There are over 30 kinds of Muscular Dystrophy. Some forms of Muscular Dystrophy affect involuntary organs like the heart. This muscular disease can be seen in during infancy or may not be known until much later on in life. Muscular Dystrophy is different for each person that has it. It may be more progressive in one person that it is another, it may start to occur much earlier in one person than another, it could be inherited in one but not another, or it can be mild to very severe and ultimately cause death.…

    • 306 Words
    • 2 Pages
    Good Essays

Related Topics