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What is the most common age of onset of myasthenia gravis?
GaleEncyofNeuroDis
The most common age at onset is the second and third decades in women and the seventh and eighth decades in men.
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∙ 13y ago
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How does thymectomy treat myasthenia gravis?
Thymectomy or thymus removal is recommended for most with this disease. Greatest benefit occurs 2 to 5 years afterwards. The best response are in young people early in the onset.
What is the single fiber electromyogram test to diagnose myasthenia gravis?
SFEMG is the most sensitive clinical test of neuromuscular transmission and shows increased jitter in some muscles in almost all patients with myasthenia gravis. Jitter is greatest in weak muscles.
How many people have myasthenia gravis in the world?
The prevalence of MG in the United States is estimated to be about 20/100,000 population. However, MG is probably under diagnosed and the prevalence may be higher. Myasthenia Gravis occurs in all races, both genders, and at any age. MG is not thought to be directly inherited nor is it contagious. It does occasionally occur in more than one member of the same family. Source: Myasthenia Foundation of America, Inc. (MGFA) http://www.myasthenia.org/amg_whatismg.cfm Taken From Article entitled: What is Myasthenia Gravis (MG)
What is the most common form of myasthenia gravis?
skeletal (voluntary) muscle weakness.eyes : drooping eyelids(ptosis) and blurred vision.mouth : difficulty in chewing, speaking, or swallowingarms, hands, finger : difficult to perform simple manual tasks.leg : standing or walking difficult.respiratory muscles : breathing problemdysphonia.The unique features of myasthenia gravis are fatigability,fluctuation of function, and restoration of function after re
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This procedure is most useful in acute, self-limited disorders such as Guillain-Barre syndrome, or when chronic disorders, such as myasthenia gravis, become more severe in symptoms.
How do corticosteroids work to treat myasthenia gravis?
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What diseases can you find in the muscular system?
Poliomyelitis - viral infection of the nerves that control skeletal muscle movement Muscular Dystrophies - (most commonly a mutation of dystrophin) muscle function is impaired, causing weakness Myasthenia Gravis - autoimmune disease affecting the neuromuscular junction.
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What are some autoimmune diseases?
Crohn's Disease, Ulcerative Colitis, Sarcoidosis, Ankylosing Spondylitis, Behcet's Disease, asthma has an autoimmune component, myasthenia gravis, and immune-mediated thrombocytopenia purpura to name a few.
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Myasthenia gravis?
DefinitionMyasthenia gravis is a neuromuscular disorder. Neuromuscular disorders involve the muscles and the nerves that control them.Alternative NamesNeuromusclar disorder - myasthenia gravis Causes, incidence, and risk factorsMyasthenia gravis causes weakness of the voluntary (skeletal) muscles. These are the muscles that create movement and are normally under your conscious control. The involuntary muscles, on the other hand, are not under conscious control (such as the muscles of your heart and many other internal organs).In myasthenia gravis, weakness occurs because the nerve that activates a particular muscle does a poor job of stimulating that muscle. This problem occurs because immune cells (which normally attack foreign invaders) target and attack the body's own healthy cells. This is known as an autoimmune response. This autoimmune response produces antibodies that block the muscle cells from receiving messages (neurotransmitters) from the nerve cell.The cause of autoimmune disorders such as myasthenia gravis is unknown. In some cases, myasthenia gravis may be associated with tumors of the thymus (an organ of the immune system). Patients with myasthenia gravis have a higher risk of having other autoimmune disorders, such as thyrotoxicosis, rheumatoid arthritis, and systemic lupus erythematosus (lupus).Myasthenia gravis can affect people at any age. It is most common in young women and older men.SymptomsThe muscle weakness of myasthenia gravis worsens with activity and improves with rest. Weakness in affected muscles may cause:Breathing difficulty because of weakness of the chest wall musclesChewing or swallowing difficulty, causing frequent gagging, choking, or droolingDifficulty climbing stairs, lifting objects, or rising from a seated positionDifficulty talkingDrooping headFacial paralysis or weakness of the facial musclesFatigueHoarseness or changing voiceWeakness of the eye muscles, causing Double visionDifficulty maintaining steady gazeEyelid droopingSigns and testsA neurological examination may be normal or may show muscle weakness that progressively worsens as the muscle is used. In many people with myasthenia gravis, the eye muscles are affected first. Reflexes and feeling (sensation) are normal. Weakness may affect the arms, legs, breathing or swallowing muscles, and any other muscle group.Tests that may be performed:Acetylcholine receptor antibodies (may be present in the blood)CT or MRI scan of the chest (may show a tumor in the thymus)Repetitive stimulation (a type of nerve conduction study, may be more sensitive)Single-fiber EMG (may be very sensitive)TreatmentThere is no known cure for myasthenia gravis. However, treatment may result in prolonged periods without any symptoms (remission).Lifestyle adjustments usually enables continuation of many activities. Activity should be planned to allow scheduled rest periods. An eye patch may be recommended if double vision is bothersome. Stress and excessive heat exposure should be avoided because they can worsen symptoms.Some medications, such as neostigmine or pyridostigmine, improve the communication between the nerve and the muscle. Prednisone and other medications (such as azathioprine, cyclosporine, or mycophenolate mofetil) that suppress the autoimmune response responsible for the weakness may be used if symptoms are severe and other medications don't work well enough.Plasmapheresis may reduce symptoms for 4 - 6 weeks and is often used before surgery. In this technique, the person's blood plasma (the clear part of the blood) containing the antibodies is removed from the body and replaced with donated, antibody-free plasma or with other intravenous fluids.Intravenous immunoglobulin infusions may be as effective as plasmapheresis. In this technique, a large volume of a mixture of helpful antibodies is given directly into the bloodstream to blunt the effect of the autoimmune antibodies.Surgical removal of the thymus (thymectomy) may result in permanent remission or less need for medicines, especially when there is a tumor present.Patients with eye problems may try lens prisms to improve vision. Surgery may also be performed on the eye muscles.Several medications may make symptoms worse and should be avoided. Therefore, it is always important to check with your doctor about the safety of a medication before taking it.Crisis situations, where muscle weakness involves the breathing muscles, may occur without warning with under- or overuse of medications. These attacks seldom last longer than a few weeks. Hospitalization and assistance with breathing may be required during these attacks. Often plasmapheresis is used to help end the crisis.Support GroupsThe stress of illness can often be helped by joining support groups where members share common experiences and problems. See myasthenia gravis - support group.Expectations (prognosis)There is no cure, but long-term remission is possible. There may be minimal restriction on activity in many cases. People who have only eye symptoms (ocular myasthenia gravis), may develop generalized myasthenia over time.Pregnancy is possible for a woman with myasthenia gravis but should be closely supervised. The baby may be temporarily weak and require medications for a few weeks after birth but usually does not develop the disorder.ComplicationsComplications of surgeryMyasthenic crisis (breathing difficulty), may be life threateningRestrictions on lifestyle (possible)Side effects of medications (see the specific medication)Calling your health care providerCall your health care provider if you develop symptoms of myasthenia gravis.Go to the emergency room or call the local emergency number (such as 911) if you have breathing difficulty or swallowing problems.ReferencesBenatar M, Kaminski HJ. Evidence report: the medical treatment of ocular myasthenia (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2007;68(24):2144-9.Vincent A, Newsom-Davis J. Disorders of neuromuscular transmission. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier. 2007: chap 448.Zinman L, Ng E, Bril V. IV immunoglobulin in patients with myasthenia gravis: a randomized controlled trial. Neurology. 2007;68(11):837-41.
