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+myasthenia gravis pathophysiologie
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Myasthenia gravis (MG) is a chronic state that causes muscles to tire and weaken easily. The meaning of the term Myasthenia Gravis is broken up, My means Muscle, asthenia means lack of strength and Gravis means serious. In an autoimmune disorder the immune system attacks parts of the body. The part of the body that is attacked by the circulation of antibodies, is the muscular system, and in certain receptors for acetylcholine on muscle cells at the neuromuscular junctions.
An overview of the disease:
MG patients have only one-third of the normal numbers of acetylcholine receptors which causes weak and easily fatigued muscles. The muscles under voluntary control are affected. The heart muscles, which are under involuntary control, are not affected. In MG generally, the muscles that control the eye and eyelid movement are affected first, causing the eyelids to sag. Some MG patients may develop double or blurred vision. When only the eye muscles are affected, the disease is known as Ocular Myasthenia. Disease symptoms affecting the facial muscles leads to limitations of facial expressions. Victims have difficulty smiling and expressing emotions on their face.
When the throat muscles are affected, this causes problems with speech, swallowing , and chewing. Patients may choke easily and their speech is often nasal due to the weakness of the velar muscles. The arm and leg muscles may weaken affecting activities like lifting or walking, with some patients appearing to wobble. There may be a loss of balance and an uncoordinated walk. It would be difficult to hold or grab on to objects with weakened arm muscles. Approximately 15% of MG patients have a thymoma. In most cases the tumour is not harmful and can be treated. Breath...
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... are sent through the electrodes to measure how well the nerves can send a signal to the muscle and to determine whether signals get worse when the muscle is tired.
Single-fiber electromyography: Measures the electrical activity that flows between the brain and the muscle.
Magnetic Resonance Imaging: This scan may be performed to identify a thymoma.
Prophylaxis or treatment of the disease
Firstly you could remove the thymus gland which oversees much of the immunes response. Secondly, create intravenous antibodies to bind and inactivate the ones causing the damage. Thirdly, you could invest in cholinesterase inhibitors to improve communication between nerves and muscles which helps the affected muscles contract properly and maintain good strength. You could also do a plasma exchange transfusion which rapidly removes the damaging antibodies from the circulation.
As said before DMD weakens the diaphragm and intercostal muscles. These muscles aid in respiration, therefore he has a difficult time expanding his lungs making him prone to infections. Also, since he cannot control his respiratory muscles it may cause him to swallow food and aspirate it into his lungs creating obstructions in his respiratory tract. There may be a lot of different pulmonary infections James is going to be prone to because of this.
Last segment in data collection was to analyze the effects of direct electrical stimulation. The hook electrode was disconnected and two electrode needles were inserted about five mm from each end of the gastrocnemius muscle. Starting at the maximum voltage from the first experiment, voltage was slowly increased until a twitch appeared. Then voltage was set ten times the maximum voltage from the first experiment. For both experiments, data were collected for thirty
"Duchenne Muscular Dystrophy: MedlinePlus Medical Encyclopedia." U.S National Library of Medicine. U.S. National Library of Medicine. Web. 20 May 2014.
The muscle selected for the biopsy depends on the location of symptoms that may include pain or weakness. The muscles often selected for sampling are the bicep (upper arm muscle), deltoid (shoulder muscle), or quadriceps (thigh muscle).
Symptoms: Up to the age of 1-3 years, affected boys have normal muscles that is they learn to stand and walk later than they are supposed to do and speech may be slow in development. Gowers sign is a sign that can be seen in boys. Hypertrophy of the calf muscles is also a characteristic sign of DMD (Alan E H Emery., 1998). Contractures at the knees and elbows are common and it will lead most boys to use wheelchairs by the age of 10, and end them dead before or at the age of 20. The commonest cause of death is cardiac muscles involvement that will lead to cardiac faliure and subsequentl to respiratory failure (Pryse-Phillips, William E. M. and Murray, T. J., “ A concise textbook Essential Neurology”. 4th ...
As motor neurons degenerate, this obviously means they can no longer send impulses to the muscle fibers that otherwise normally result in muscle movement. Early symptoms of ALS often include increasing muscle weakness, especially involving the arms and legs, speech, swallowing or breathing. When muscles no longer receive the messages from the motor neurons that they require to function, the muscles begin to atrophy (become smaller). Limbs begin to look thinner as muscle tissue atrophies (Choi, 1988).
Because symptoms are wide - ranged and studies for treatment of FMS did not begin until the 1980's, it is one of the most popularly misdiagnosed conditions in the medical world. The main symptoms are widespread pain and fatigue as well as tender points on the body. The muscular pain often may feel like a pulled muscle and may burn or twitch. (Source 3)
A rare and severe disease, Guillain Barre Syndrome, often occurs after an acute infectious procedure. Guillain Barre Syndrome affects the peripheral nervous system. Normally, it is an acute form of paralysis in the lower body area that moves to the upper limbs and face. Over time, the patient will lose all his reflexes and goes through a complete body paralysis, unless maintained in a prompt manner. Guillain Barre Syndrome is a life threatening disorder and needs timely treatment and therapy with intravenous immunoglobulin’s. Unfortunately many people can lose their lives without proper and prompt medical treatment. “Dysautonomia and pulmonary complications are the basic reason for death for those contract GBS, luckily these kind of complications are rare..” Guillain-Barre syndrome is a disorder that your ownbody's immune system attacks your nerves. The first symptoms usually consist of weakness and or tingling in lower extremitites as well as the hands. These symptoms can quickly spread, eventually paralyzing your whole body. It is unknown what the exact cause of Guillain-Barre syndrome is unknown, but it is more than often preceded by an infectious illness such as the stomach flu or a respiratory infection. Guillain-Barre syndrome is an uncommon disorder, affecting roughly only one or two people per 100,000. There are several treatments and therapies that can help ease symptoms and reduce the duration of the illness and although most people recover from Guillain-Barre syndrome, many people may still experience lingering effects from it, such as numbness, fatigue or weakness.
Based on the apparent symptoms of the elderly patient consisting of muscle weakness and a drooping of the eyelids, it appears that the cause of illness is myasthenia gravis, a condition that weakens the voluntary muscles of the body. The cause of this eyelid drooping, or muscle paralysis in general, is due to a misstep in the flow from the nerve fiber to the muscle fiber. It is known that an action potential in the muscle fiber is required for muscle contraction. However, if the release acetylcholine is blocked, or the number of acetylcholine receptors is reduced, it causes a chain of events that prevent muscle contraction. This prevention of the binding of acetylcholine to the receptor prevents
For some types of MD, medication can help. Guys with Duchenne MD may be helped by a medicine called prednisone, and teens with myotonic MD might use mexilitine to relax muscles.
According to Medical-Surgical Nursing: 7th edition, Myasthenia Gravis (MG) is an autoimmune disease that can be considered as a chronic neuromuscular disorder (Lewis et al., 2007, p. 1555). MG is caused by an autoimmune process in which “antibodies attack acetylcholine (ACh) receptors, resulting in a decreased number of ACh receptor (AChR) sites at the neuromuscular junction” (p. 1555). Due to the neurotransmitter’s inability to connect the muscles and the nerves, it is difficult for the muscle to contract. This disease basically causes muscle fatigue and therefore a detrition of muscle strength over time. (John Hopkins Medicine, n.d.) In many respects, it is like a satellite unable to detect a signal when it is blocked by interfering radio waves.
According to the MediLexicon Medical Dictionary, muscular dystrophy is defined as a general term for a number of hereditary, progressive degenerative disorders affecting skeletal muscles, and often other organ systems (Staff). Basically what that means is that muscular dystrophy is a genetic disorder that is passed down that affects the skeletal muscles and other organs by slowly breaking them down. Since it is genetic, it is not contagious and you cannot catch it from someone who has it. MD weakens muscles over time, so children, teens, and adults who have the disease can gradually lose the ability to do the things most people take for granted, like walking or sitting up. Someone with MD might start having muscle problems as a baby or their symptoms might start later. Some people even develop MD as adults (Clark, 2010).
With motor neurone disease it attacks the nerves, in the brain and spinal cord. This means messages gradually stop reaching muscles, which leads to weakness and wasting. In the case study the
When a person begins to suffer from Guillain- Barre Syndrome their myelin sheath of their nervous system is being attacked and destroyed by the immune system (NINDS, 2011). The myelin sheath begins to lose its ability to transmit signals rapidly and affectively. Since signals are not getting transmitted to the brain fast enough, a person begins to notice fewer sensory responses from the rest of the body (NINDS, 2011). A person wouldn’t be able to tell right away or at all if an item they are touching is hot, cold, or causing pain. There also wouldn’t be good signal transmission from the brain to the rest of the body (NINDS, 2011). There would be signs of the muscles being unable to respond to the weakened or distraught signals they were receiving. Since the myelin sheath is responsible for transmitting the signals from a long distance, the upper and lower extremities would be the first to show signs of muscle dysfunction.
Myasthenia Gravis (MG) is an autoimmune disorder affected the neuromuscular junction and the process of neuromuscular transmission. MG is a disease that reflects an autoimmune response against acetylcholine (ACh) receptors at the postsynaptic membrane at the motor endplate (Duffy, 99). Because there are a reduced number of operative receptors, the muscle responsiveness to the Ach that sparks muscle contraction is reduced. The repercussion for this is diminishing muscle contractions with repetition of use. With rest and time for nerves to reload the Ach supply, strength of the muscles may improve.