The epidemiology of myasthenia gravis. 1994

L H Phillips
Department of Neurology, University of Virginia Medical School, Charlottesville.

This review has attempted to show what the patient population with MG really looks like. Generalizations about the manifestations of the disease may not be accurate if they are derived from small numbers of patients. The epidemiologic "big picture" provides a more realistic overview of the disease. There are surprisingly fewer patients with MG than many experienced clinicians expect. This does not diminish the impact of the disease on the individual patient, but it does give a more realistic view of its place among diseases affecting the nervous system. This knowledge can be used to direct the approach to the disease in the future. The fact that the number of patients with the disease is increasing in older age groups is a tribute to the success of treatment strategies during the past 20 years. As a consequence, the typical patient with MG in the future will likely be older and have additional medical problems. The evolution of our treatment in the future will need to take this factor into consideration. Older patients may not tolerate the aggressive immunosuppressive regimens that benefit young patients. Ideally, more targeted types of therapies that suppress a specific immunologic abnormality without imposing the burden of side effects inherent in present treatments will be most beneficial to these patients.

UI MeSH Term Description Entries
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009157 Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. Anti-MuSK Myasthenia Gravis,MuSK MG,MuSK Myasthenia Gravis,Muscle-Specific Receptor Tyrosine Kinase Myasthenia Gravis,Muscle-Specific Tyrosine Kinase Antibody Positive Myasthenia Gravis,Myasthenia Gravis, Generalized,Myasthenia Gravis, Ocular,Anti MuSK Myasthenia Gravis,Generalized Myasthenia Gravis,Muscle Specific Receptor Tyrosine Kinase Myasthenia Gravis,Muscle Specific Tyrosine Kinase Antibody Positive Myasthenia Gravis,Myasthenia Gravis, Anti-MuSK,Myasthenia Gravis, MuSK,Ocular Myasthenia Gravis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000367 Age Factors Age as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or the effect of a circumstance. It is used with human or animal concepts but should be differentiated from AGING, a physiological process, and TIME FACTORS which refers only to the passage of time. Age Reporting,Age Factor,Factor, Age,Factors, Age
D012720 Severity of Illness Index Levels within a diagnostic group which are established by various measurement criteria applied to the seriousness of a patient's disorder. Illness Index Severities,Illness Index Severity
D014481 United States A country in NORTH AMERICA between CANADA and MEXICO.

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