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不完全川崎病研究进展 被引量:2

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摘要 川崎病(KD)又称皮肤黏膜淋巴结综合征(MCLS),是一种急性、自限性、自身免疫性血管炎综合征。确切发病机制目前尚不清楚,大多数学者认为可能是由病原微生物入侵具有遗传易感性的患儿,通过超抗原、热休克蛋白等触发体内异常免疫反应而引起。
作者 陈静 范晓晨
出处 《山东医药》 CAS 2012年第40期90-92,共3页 Shandong Medical Journal
基金 安徽省卫生厅自然基金资助项目(09A023)
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参考文献17

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二级参考文献25

共引文献88

同被引文献21

  • 1张清友,杜军保.不完全川崎病的诊治现状[J].中华儿科杂志,2006,44(5):339-341. 被引量:149
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