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遗传性 Q-T 延长综合征在国内已见报道。本病心电图表现:Q-T 间期显著延长,TU 畸形,出现 RT 重叠现象,伴尖端扭转型室性心动过速。临床可发作昏厥及猝死。如能正确诊断及时治疗,可使患者免于意外。我院最近发现本病在同一家族中四例病人,报道如下。病历摘要郭××,男,14岁,初中学生,住院号84123,1977年7月20日入院。病史:反复发作性昏厥六年。患者8岁时,
Hereditary Q-T extended syndrome has been reported in China. The ECG showed: Q-T interval was significantly prolonged, TU deformity, RT overlap phenomenon with torsades de pointes ventricular tachycardia. Clinical onset of syncope and sudden death. If the correct diagnosis of timely treatment, patients can be free from accidents. Our hospital recently found that the disease in the same family of four patients, reported as follows. Medical records Guo × ×, male, 14 years old, junior high school students, hospital number 84123, July 20, 1977 admission. History: repeated episodes of fainting for six years. When the patient is 8 years old,