| Literature DB >> 17310034 |
F Deymeer1, O Gungor-Tuncer, V Yilmaz, Y Parman, P Serdaroglu, C Ozdemir, A Vincent, G Saruhan-Direskeneli.
Abstract
We compared 65 anti-acetylcholine receptor (AChR)-negative myasthenia gravis (MG) patients, including 32 anti-muscle-specific tyrosine kinase (MuSK)-positive (49%) and 33 anti-MuSK-negative (seronegative) (51%) patients, with 161 anti-AChR-positive MG patients. The anti-MuSK-positive group had a higher frequency of bulbar involvement and respiratory crises. The seronegative group was in between the anti-MuSK positive and the anti-AChR positive groups, being closer to the latter, with regard to the severity of the disease. At the end of follow-up, the outcome of the anti-MuSK-positive patients was not different from that of the anti-AChR-positive patients, although their maintenance corticosteroid dose was higher. The seronegative patients had better outcome than the other two groups.Entities:
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Year: 2007 PMID: 17310034 DOI: 10.1212/01.wnl.0000254620.45529.97
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910