Myasthenia gravis Is an autoimmune disorder mainly caused by antibodies to
the muscle acetylcholine receptors (AChRs) at the neuromuscular junction. L
oss of these receptors leads to a defect in neuromuscular transmission with
muscle weakness and fatigue. AChR antibody tests are widely available and
overall incidence and prevalence of the disorder seem to be rising, especia
lly in elderly people. The disease is heterogeneous with respect to age at
onset, thymic changes and distribution of muscle weakness, but the roles of
immunogenetic factors and thymic abnormalities in the causes of the differ
ent forms are unclear. Most patients are now effectively treated with choli
nesterase inhibitors and immunosuppressive drugs, and in younger patients b
y thymectomy. In about 15% of patients with myasthenia gravis, AChR antibod
ies are absent, and many of these patients have antibodies to another neuro
muscular junction protein, muscle specific kinase (MuSK). Myasthenia needs
to be distinguished from other rarer but equally well characterised autoimm
une, genetic, and toxic disorders of neuromuscular transmission by clinical
and laboratory tests.