Myasthenia gravis is an autoimmune disorder characterized by weakness and fatigue of skeletal muscles that worsens with use. It results from a decrease in acetylcholine receptors caused by circulating antibodies against the receptors, which compete with acetylcholine to bind receptors, induce receptor endocytosis, and damage the postsynaptic membrane. Treatment includes administering acetylcholinesterase inhibitors to prolong the action of acetylcholine at the neuromuscular junction, thymectomy to remove thymus tissue mediating immune responses, immunosuppression with drugs like glucocorticoids and azathioprine, and plasmapheresis to remove acetylcholine receptor antibodies from the plasma.