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肌肉特异性酪氨酸激酶抗体与重症肌无力 被引量：4

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摘要 重症肌无力(MG)是一种主要累及神经肌肉接头突触后膜乙酰胆碱受体(acetylcholine receptor,AChR)的自身免疫性疾病。近来研究发现肌肉特异性酪氨酸激酶(muscle-specific kinase,MuSK)抗体(MuSK Ab)与MG发病机制有关。MuSK Ab阳性MG临床表现和治疗与血清AChR(+)MG存在明显不同。MuSK Ab阳性MG病情重,容易引起漏诊和误诊。
作者 王中魁 魏东宁
机构地区 解放军总医院第二附属医院神经内科
出处 《中国神经免疫学和神经病学杂志》 CAS 2009年第6期442-444,共3页 Chinese Journal of Neuroimmunology and Neurology
关键词 重症肌无力 肌肉特异性酪氨酸激酶抗体 乙酰胆碱受体抗体
分类号 R746.1 [医药卫生—神经病学与精神病学]
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参考文献17

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同被引文献65

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引证文献4

二级引证文献9

中国神经免疫学和神经病学杂志
2009年 第6期

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