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1957年Jervell 与Lange-Nielson 首次报告先天性耳聋病人合并Q—T 间期延长,可由情绪激动或劳累促发心室颤动而致昏厥,也称为心脏～听觉或耳聋～心脏综合征。后来发现无耳聋者也可有类似心脏综合征的表现。由于该综合征主要特点是在心电图上Q-T 间期延长,故统称为Q-T 延长综合征。该综合征长期以来被认为是先天性疾病,后来通过尸体解剖资料的积累,于1978年由James 提出该综合征的部分病例可由病毒感染所引起。本文报告一例经尸体解剖和病毒分
In 1957, Jervell and Lange-Nielson first reported congenital deafness patients with Q-T interval prolongation, may be caused by agitation or fatigue ventricular fibrillation and fainting, also known as heart-hearing or deafness ~ heart syndrome. Later found no deafness may also have a similar performance of heart syndrome. Because of the main features of the syndrome in the ECG Q-T interval is extended, it is collectively referred to as Q-T extended syndrome. The syndrome has long been considered a congenital condition, and later by the accumulation of autopsy data, in 1978 by James suggested that some cases of the syndrome can be caused by a viral infection. This article reports a case of necropsy and virus division