Myasthenia Gravis Research Paper

Fibromyalgia Syndrome (FMS) is a musculoskeletal illness (which causes chronic pain) and a chronic fatigue disorder. It can also change sleep patterns and cause the following: digestive disorders, chronic headaches, painful menstrual periods, temperature sensitivity, morning stiffness, numbness or tingling of extremities, and even cognitive memory problems. The name fibromyalgia comes from "fibro" in Latin meaning tissue, "my" in Greek meaning muscle, and "algia" (also Greek) meaning pain.(source 5)

It happens when your nerve endings fail to interact properly with your muscles. MG usually affects the muscles of the eyes, face, neck, arms, and legs. MG is most common in young women 20 to 30 years of age, and in men 60 to 70 years of age.(Myasthenia) What makes this relevant is that Myasthenia Gravis can be developed in the human body if you are exposed to neurotoxins like Sarin. On base by the Syrian border, sirens were triggered daily and the officials at the base said that they were false alarms even though they knew that they were not. “A woman named Tracy Elledge, a former combat engineer and one of the veterans I interviewed, said, “Alarms went off all the time.… Our officers told us they were false and to disconnect

     Recent studies show that this syndrome may be associated with changing craniofacial and skeletal muscle metabolism, such as blood flow, which causes the chronic fatigue and severe weakness. Another hypothesis is that an infectious trauma to the body, such as a virus, triggers the illness. However, with this syndrome being new, no specific virus has been identified. There is though a plot study that shows that there is possible inherited tendency toward the disease. This disease/syndrome has increased

Myasthenia Gravis (MG) is a chronic autoimmune disorder of the neuromuscular system part of the body. Chronic means persisting for a long time or constantly recurring. Autoimmune disorder is the confusion of the body’s immune system. The immune system form antibodies that mistakenly identify healthy tissue as foreign and then, the antibodies will attack and/or destroy healthy body tissue. Neuromuscular is the nervous system relationship with the muscles bring about body movement.

2006). The onset of this illness usually occurs in the latter stages of life after the age of 50

Abstract: we report a case of 63 years-old man affected by myasthenia gravis associated to two nodular lesions of thymic tissue and, after complete thymothymomectomy, pathologic findings revealed a B3 thymoma and a clear cell carcinoma. Post-operative period was uneventful. The patient had no recurrence or metastasis after the first year of follow-up.

Myasthenia gravis may affect any voluntary muscles. They may affect muscles that control the eyelid movement, facial expression and swallowing. The most symptoms of myasthenia gravis that can be noticed are the weakness of the eye muscle that causes double vision. Some symptoms of myasthenia gravis may include unstable walk, arm weakness, weakness in hands, fingers, legs and neck, change in facial expression, having a hard time swallowing, shortness of breath, and having problems with

The mechanism of how bruxism may result in muscular disorders can be explained as follows: The impairment of blood flow and swelling caused by increased intramuscular pressure analogous to other muscles, which results in masticatory muscle discomfort and pain during and instantly after a sustained contraction; However the exertional pain declines rapidly once the muscle relaxes and blood flow is restored again. One of the characteristics of

In the world today, there are approximately about 10 in one million people who are affected by the disease called myositis. With it being a rare, myositis is a disease in which the skin and muscle fibers become damaged or inflamed which result in muscle weakness. There are many different types of myositis along with causes, symptoms, diagnosis, and treatments.

Myasthenia gravis (MG) is considered to be a very rare disorder. It is an autoimmune neuromuscular junction disease which in most cases occurs as a painless, massively fatigable weakness; targeting certain muscle groups. Some of the initial presentations of myasthenia gravis include the ocular weakness with binocular diplopia consecutively, along with asymmetric ptosis. Limb weakness is rare initially. Therefore, patients who experience ocular weakness as an initial symptom, usually do not develop the limb weakness until approximately three years later. Therefore, a primary care doctor must be strictly observant so as to find out the presence of myasthenia gravis. When the T cells-dependent immunologic react or attack the endplate area of the

Myasthenia gravis can be classified as a chronic neurologic disease of the neuromuscular transmission and characterized by presentation of fatigable muscle weakness to the external ocular, cranial, respiratory and limb muscles (Smith, C., P.A.-C., & Stickler, D., M.D. 2012). The incidence of this disease is about 20 per 100,000 people in various populations, affecting mostly women in their 20’s to 30’s and men over the age of 60 (Postevka 2013).

Guillain-Barre Syndrome, or acute inflammatory demyelinating polyneuropathy, is a self-limiting disease characterized by areflexia and acute progressive motor weakness of at least one limb. Other symptoms include motor weakness of the extremities and face, loss or reduction of deep tendon reflexes, decreased sensation throughout the body,ophthalmoplegia, and ataxia. In severe cases respiratory failure and autonomic dysfunction may occur. Respiratory failure results from the demyelination of the phrenic and intercostal nerves. Consequently, the person loses the ability to inhale and exhale. Autonomic dysfunction resulting from the demyelination of the sympathetic and vagus nerves can lead to cardiac arrhythmias,

John Stillman, a thirty-two year old gymnastics instructor, was presented to the clinic with complaints of muscle weakness in the face that comes and goes. Symptoms have progressed over the past two months to include tired jaw, difficulty swallowing, diplopia in the evening, increased weakness in his limbs and shortness of breath. Physically visible, John has mild ptosis in both eyelids and his smile is a bit off. Patient John Stillman portrays symptoms of Myasthenia Gravis (MG) meaning grave muscular weakness. According to Myasthenia Gravis Foundation of America, the most common form of MG is chronic autoimmune neuromuscular disorder, which can be seen by loss of strength in the voluntary muscle groups (2015). Much research has been done for Myasthenia Gravis, but there is still a lot of unknown information, such as a cure. In this study, one will learn what Myasthenia Gravis is, how it is tested, possible complications, and how it is treated.

can be widespread in muscles it may be worsened if the muscles around the head ae stiff, which

The patient experiences this disease generally feels uncontrolled, irritating or tedious muscular contraction that leads to changed movements and abnormal position or attitudes of hands and fingers.