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.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adrenal Cortex Hormones / administration & dosage
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Adult
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Autoantibodies / blood*
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Autoantibodies / immunology*
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Biomarkers / analysis
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Biomarkers / blood
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Brain Stem / immunology
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Brain Stem / physiopathology
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Causality
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Disease Progression
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Dose-Response Relationship, Drug
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Female
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Humans
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Male
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Middle Aged
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Myasthenia Gravis / blood*
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Myasthenia Gravis / immunology*
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Myasthenia Gravis / physiopathology
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Neuromuscular Junction / drug effects
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Neuromuscular Junction / immunology
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Neuromuscular Junction / physiopathology
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Predictive Value of Tests
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Prevalence
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Receptor Protein-Tyrosine Kinases / immunology*
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Receptors, Cholinergic / immunology*
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Respiratory Insufficiency / epidemiology
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Respiratory Insufficiency / immunology
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Respiratory Insufficiency / physiopathology
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Serologic Tests
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Treatment Outcome
Substances
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Adrenal Cortex Hormones
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Autoantibodies
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Biomarkers
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Receptors, Cholinergic
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MUSK protein, human
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Receptor Protein-Tyrosine Kinases