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gMG is an autoantibody-mediated disease driven by pathogenic B cells. It causes unpredictable fatigue and muscle weakness, that can affect the eyes, mouth and throat, neck, trunk, and limbs.1-3 Review gMG symptoms
B cells produce the autoantibodies that drive gMG disease activity. These include AChR, MuSK, and LRP4 autoantibodies.3,4 Read an overview of gMG
AChR, acetylcholine receptor; LRP4, low-density lipoprotein receptor-related protein 4; MuSK, muscle-specific kinase.
Autoantibodies in gMG disrupt neuromuscular communication, resulting in impaired synaptic signaling and subsequent weakness and fatigability.4 Explore the mechanism of disease
1. Masi G, O’Connor KC. Curr Opin Neurol. 2022;35:586-596.
2. Dresser L, Wlodarski R, Rezania K, Soliven B. J Clin Med. 2021;10:2235.
3. Yi JS, Guptill JT, Stathopoulos P, Nowak RJ, O'Connor KC. Muscle Nerve. 2018;56(2):172-184.
4. Huda R. Front Immunol. 2020;11:510568.