PMID- 12849266 OWN - NLM STAT- MEDLINE DCOM- 20030828 LR - 20220318 IS - 1474-4422 (Print) IS - 1474-4422 (Linking) VI - 2 IP - 2 DP - 2003 Feb TI - Seronegative generalised myasthenia gravis: clinical features, antibodies, and their targets. PG - 99-106 AB - Myasthenia gravis (MG) is a well-recognised disorder of neuromuscular transmission that can be diagnosed by the presence of antibodies to the acetylcholine receptor (AChR). However, some patients (about 15%) with generalised MG do not have detectable AChR antibodies. There is some evidence, however, that this "seronegative" MG is an antibody-mediated disorder. Plasma from patients with the disorder seems to contain various distinct humoral factors: IgG antibodies that reversibly inhibit AChR function; a non-IgG (possibly IgM) factor that indirectly inhibits AChR function; and an IgG antibody against the muscle-specific kinase (MuSK). The presence of antibodies against MuSK appears to define a subgroup of patients with seronegative MG who have predominantly localised, in many cases bulbar, muscle weaknesses (face, tongue, pharynx, etc) and reduced response to conventional immunosuppressive treatments. Moreover, muscle wasting may be present, which prevents complete response to these therapies. FAU - Vincent, Angela AU - Vincent A AD - Department of Clinical Neurology, University of Oxford, UK. angela.vincent@imm.ox.ac.uk FAU - Bowen, John AU - Bowen J FAU - Newsom-Davis, John AU - Newsom-Davis J FAU - McConville, John AU - McConville J LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review PL - England TA - Lancet Neurol JT - The Lancet. Neurology JID - 101139309 RN - 0 (Antibodies) SB - IM MH - Antibodies/analysis/*immunology MH - Humans MH - Immunologic Tests MH - Myasthenia Gravis/diagnosis/*immunology RF - 84 EDAT- 2003/07/10 05:00 MHDA- 2003/08/29 05:00 CRDT- 2003/07/10 05:00 PHST- 2003/07/10 05:00 [pubmed] PHST- 2003/08/29 05:00 [medline] PHST- 2003/07/10 05:00 [entrez] AID - S1474442203003065 [pii] AID - 10.1016/s1474-4422(03)00306-5 [doi] PST - ppublish SO - Lancet Neurol. 2003 Feb;2(2):99-106. doi: 10.1016/s1474-4422(03)00306-5.