Myasthenia gravis natural history, complications and prognosis
Myasthenia gravis Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Myasthenia gravis natural history, complications and prognosis On the Web |
American Roentgen Ray Society Images of Myasthenia gravis natural history, complications and prognosis |
FDA on Myasthenia gravis natural history, complications and prognosis |
CDC on Myasthenia gravis natural history, complications and prognosis |
Myasthenia gravis natural history, complications and prognosis in the news |
Blogs on Myasthenia gravis natural history, complications and prognosis |
Risk calculators and risk factors for Myasthenia gravis natural history, complications and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Natural History
Complications
Prognosis
With treatment, patients have a normal life expectancy, except for those with a malignant thymoma (whose lesser life expectancy is on account of the thymoma itself and is otherwise unrelated to the myasthenia). Quality of life can vary depending on the severity and the cause. The drugs used to control MG either diminish in effectiveness over time (cholinesterase inhibitors) or cause severe side effects of their own (immunosupressants). A small percentage (around 10%) of MG patients are found to have tumors in their thymus glands, in which case a thymectomy is a very effective treatment with long-term remission. However, most patients need treatment for the remainder of their lives, and their abilities vary greatly. It should be noted that MG is not usually a progressive disease. The symptoms may come and go, but the symptoms usually do not get worse as the patient ages. For some, the symptoms decrease after a span of 3–5 years.