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Myasthenia gravis (MG) is a rare autoimmune disease characterized by specific autoantibodies targeting the postsynaptic membrane of the neuromuscular junction, resulting in fluctuating fatigability and weakness of ocular, bulbar, and skeletal muscles, with the potential for life-threatening crises [1]. MG has a bimodal incidence pattern, with younger women and older men being most commonly affected [2].
JMIR Form Res 2025;9:e58266
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