Congenital long QT syndrome is a group of familial inherited disease.
先天性Q- T间期延长综合征是一组家族遗传性疾病。
Specific ion channel mutations underline the congenital long QT syndrome (LQTS).
特定离子通道的基因突变是产生遗传性长qt综合征的基础。
Objective To explore SCN5A gene mutations in Chinese patients with congenital long QT syndrome type 3 (LQT3).
目的研究中国人遗传性长QT综合征3型（LQT3）相关基因SCN5A突变情况。
Objective to assess the feasibility, safety and effectiveness of video-assisted thoracoscopic sympathectomy (VATS) for the treatment of congenital long QT syndrome.
目的探讨经电视胸腔镜切除左胸交感神经治疗先天性QT间期延长综合征的方法和效果。
Objective to assess the feasibility, safety and effectiveness of video-assisted thoracoscopic sympathectomy (VATS) for the treatment of congenital long QT syndrome.
目的探讨经电视胸腔镜切除左胸交感神经治疗先天性QT间期延长综合征的方法和效果。
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