Myasthenia Gravis Research Paper

Improved Essays
Myasthenia gravis is a neurological disorder that affects the immune system and causes chronic muscle weakness in the skeletal muscles of the human body. The name myasthenia gravis means "grave muscle weakness". A strong indication of myasthenia gravis is muscle weakness that heighten during periods of physical activity and decrease after resting periods. Muscles like those that control eye and eyelid movement, facial expression, eating, speaking, breathing and neck and limb movements can all be affected by myasthenia gravis.
Myasthenia gravis is caused by an irregularity in the transmission of nerve impulses to muscles. It appears when the communication between nerves and muscles is disturbed. The nerve endings will usually release a neurotransmitter substance called acetylcholine to the body’s muscles. Acetylcholine generates a muscle contraction. Those with myasthenia gravis have an absence of acetylcholine. In the case of myasthenia gravis, the body’s antibodies stop, change, or kill the acetylcholine receptors, inhibiting the muscle from contracting.The immune system creates these antibodies to fight off infection.
…show more content…
Medications used to treat the disorder include neostigmine and pyridostigmine, prednisone, azathioprine, cyclosporin, mycophenolate mofetil, and tacrolimus. These medications can boost the strength of muscles by quelling the creation of irregular antibodies. The use of these drugs must be carefully noted by a doctor because they might cause major side effects. Thymectomy is recommended for individuals with thymomas. A thymectomy is the surgical removal of the thymus gland. Other therapy treatments for myasthenia gravis include plasmapheresis and high-dose intravenous immune globulin. A neurologist will determine which treatment option is best for each person depending on the intensity of the muscle weakness, what muscles are affected, and the age of the

Related Documents

  • Great Essays

    Introduction What is carpal tunnel syndrome? Well basically carpel tunnel syndrome is a disease where the patient feels a tingling sensation in their hands and arms. He might feel that his hand or arm has gone numb. This disease is mainly caused by the twisting of the nerve that goes to the wrist of the patient. This problem can be caused due to a number of reasons, including the nature of the work done by the hands, the forceful and sudden movements of the hands even sudden jerks done to the hand can cause carpet tunnel syndrome.…

    • 4019 Words
    • 17 Pages
    Great Essays
  • Improved Essays

    Nt1310 Unit 1 Assignment

    • 449 Words
    • 2 Pages

    My choice for a genetic disorder is Spinal Muscular Atrophy also known as SMA. SMA is an inherited or genetic disorder that affects spinal motor neurons. Without these properly functioning neurons, patients have increased muscle weakness. In some severe cases patients will lose the ability to breath or swallow on their own. According to the National Human Genome Research Center, 1 in 6,000 to 1 in 10,000 people are affected by SMA.…

    • 449 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Only 1 in 100,000 people have to experience this scarce syndrome; Guillain Barre could possibly temporary have a serious affliction on the individual’s life, some of which we have heard of. Take Franklin D. Roosevelt for example, he suffered from Guillain Barre or also commonly known as “GBS” experienced a fight with this nerve damaging infection. GBS progressively starts to own a person’s life, being educated about this disease, the symptoms and effects, and the treatments will be beneficial. Two brilliant scientists discovered this syndrome, they found out what the syndrome is, and how the doctors could start diagnosing patients. Guillain Barre syndrome affects an individual’s nervous, immune and most likely the muscular system.…

    • 843 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Grade 1 means there is only mild myotonia, while grade 3 represents the more severe state of myotonia (Colding-Jorgensen 2005). Individual with Thomsen's Disease will experience muscle stiffness and delayed time in muscle relaxation (Facts about myopathies 2012). This usually interfered with daily activities of walking and eating (Facts about myopathies 2012). However, it can be manage with proper exercise and medications (Facts about myopathies 2012). With proper physical therapy, the effect of myotonia can be reduced (NINDS Myotonia 2011).…

    • 687 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    This results in muscle weakness and contributes to the characteristic presentation seen in individual’s affected about…

    • 945 Words
    • 4 Pages
    Superior 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
  • Decent Essays

    Rhabdomyolysis Rhabdomyolysis is a condition that results from the breakdown of muscle fibers. When the muscle is damaged, a substance called myoglobin is released into the bloodstream. This substance normally helps the muscle use oxygen. When released into the bloodstream, it is filtered out of the bloodstream by the kidneys.…

    • 241 Words
    • 1 Pages
    Decent Essays
  • Improved Essays

    Myasthenia Gravis affect the muscle making life difficult for those people who has it. Science thinks that MG cannot be inherited. The diagnosis of Myasthenia Gravis test your reflexes, muscle strength, muscle tone, senses of touch, sings coordination and balance. The discovery of the disease depends on the weakness of the muscle. Myasthenia gravis target the communication point between the nerve and the muscle called neuromuscular junction.…

    • 601 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    However treatment is influenced by the location and amount of the intestines are affected. Drug therapy consist of prescription anti-inflammatory drugs such as sulfasalazine or remicade to prevent inflammation in the body. This is generally reserved for newly diagnosed patients with mild symptoms Corticosteroids help to reduce the immune systems activity. Drugs like hydrocortisone, budesonide, or prednisone are given to patients with moderate to severe symptoms. Immune system suppressors which decreases action of the immune system, decreasing inflammation of the intestines in the process.…

    • 1005 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Another illness is Lambert-Eaton myasthenic syndrome in which divalent IgG antibodies cross link the presynaptic voltage-gated calcium channels, disrupting the normal parallel architecture of the channels, and reducing the number of active zone complexes (Shillito et al., 2004). This ultimately results in the amount of Acetylcholine released into the synapase. This syndrome usually occurs in middle-aged patients , and it is reported as rare in children(Hirsch,2007). According to Neuromuscular junction in health and disease by N. P. Hirsch (2007), 50 percent of the cases are associated with small cell carcinoma of the bronchus (C-LEMS). Carcinoma of bronchus is also known as lung cancer or a lung carcinoma.…

    • 269 Words
    • 2 Pages
    Improved Essays
  • Improved Essays

    Crohn's Disease

    • 749 Words
    • 3 Pages

    A newer type of corticosteroid, budesonide, has shown to work faster and also has fewer side effects. Although corticosteroids have proven to be effective in some cases, they are only meant for short term use (three to four months). Other types of drugs that work in the treatment include immune system receptors, oral 5-aminosalicylates and more. Another form of treatment for the disease includes nutrition therapy. The patient’s physician may recommend enteral or parenteral nutrition.…

    • 749 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    Cases: 1. A 13-year-old male presents with a two-year history of progressive weaknesses in both upper and lower extremities. He finds it difficult to lift heavy objects off a shelf. When sitting on the floor he has to hold onto objects such as a chair to pull himself up. On examination, there is significant wasting of muscles in the shoulders, upper arms, and hips.…

    • 1545 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    Fibromyalgia

    • 840 Words
    • 4 Pages

    A widely misunderstood and sometimes misdiagnosed chronic condition commonly characterized by widespread muscle pain, fatigue, concentration issues and sleep problems is known as Fibromyalgia. For the longest time muscle pains have been known as rheumatism and then as muscular rheumatism. Rheumatism is any disease marked by inflammation and pain in the joints. People who have been diagnosed with rheumatoid arthritis and lupus are at increased risk of also developing fibromyalgia. Fibra (Latin) means fibrous tissue and has to do with painful tendons and ligaments, Myos (Greek) means muscles, Algos (Greek) means pain.…

    • 840 Words
    • 4 Pages
    Improved Essays
  • Decent Essays

    Objective 1: Clinical Manifestation & Risk Factors • Rhabdomyolysis occurs due to the breakdown of muscle tissue o Muscle breakdown causes myoglobin to enter the bloodstream which can lead to kidney damage (Miller, n.d). • Creatine Kinase (CK) o Is an enzyme released by damaged muscle. CK is used to diagnose and follow muscle disease (Miller n.d). • Aspartate transaminase & alanine transaminase o Elevated levels of may be due to damaged muscles or overworking the muscles (Sjogren 2007).…

    • 658 Words
    • 3 Pages
    Decent Essays
  • Superior Essays

    Duchenne’s muscular dystrophy Duchenne’s Muscular Dystrophy Zachary Uecker Genetic Disease Abstract Duchenne’s muscular dystrophy is a genetic disease that targets skeletal muscles and over time, the muscles lose protein and are replaced by fats and connective tissue, making the skeletal muscles unusable. In this paper, the parts of Duchenne’s that will be covered are the method of transmission, statistics about Duchenne’s in the population, the pathophysiology, the body systems effected, signs and symptoms, age of onset, treatment/therapy options, psychological factors, prognosis, prevention techniques, ethical considerations, and how genetic counseling may be utilized for patients.…

    • 1182 Words
    • 5 Pages
    Superior Essays