The clinical research progress of non?motor symptoms in myasthenia gravis / 中华神经科杂志

ABSTRACT

Myasthenia gravis (MG) is an acquired autoimmune disease involving neuromuscular junctions transmit dysfunction. The main clinical manifestations are partial or systemic skeletal muscle weakness and extreme fatigue, increased symptoms after activity, relieved after rest and treatment with cholinesterase inhibitors. However, recent studies have found that patients of MG are not only accompanied by motor symptoms such as muscle weakness and dysphagia, but also with non?motor symptoms. This article reviews the clinical research progress of non?motor symptoms in MG.