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扩张型心肌病发病机制及治疗进展 被引量:6

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摘要 扩张型心肌病(DCM)对心脏功能影响大,多数病患终末期表现为失代偿性充血性心力衰竭,且病程中易并发恶性心律失常及猝死事件[1]。患者发病后5~10年生存率仅30%~40%[2],严重影响患者的生存质量及生命周期。DCM发病过程缓慢、隐匿,是多种复杂因素如病毒感染、毒物或药物、遗传因素、免疫系统功能紊乱、心肌细胞控制基因异常等共同影响的结果。
出处 《中国乡村医药》 2017年第19期83-84,共2页
作者简介 通信作者:刘振良,Email:393928038@qq.com
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