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家族性Q-T间期延长综合征又称Jervell-Lange-Nielsen综合征或Romano-Ward综合征,多数人认为有遗传性.我院曾遇1例,用心得安治疗获得了显著的疗效.报告如下. 患者,男,19岁.因反复发生晕厥4天于1986年10月24日入院.4天前出现无明显诱因的心悸、胸闷、头昏、乏力,约半小时后突然意识丧失,四肢抽搐,双眼凝视,小便失禁,但无口吐泡沫,约2分钟后苏醒。起病4天来晕厥发作10余次。每次发作约2～3分钟,常为活动所诱发.4年前曾类似发作2次,并因此辍学.体检:血压正常,神志清楚,瞳孔等大等圆,光反射良好.颈软,病理反
Familial QT prolongation syndrome, also known as Jervell-Lange-Nielsen syndrome or Romano-Ward syndrome, most people think that hereditary .Has been encountered in our hospital in 1 case, the use of propranolol therapy obtained significant effect. The patient, male, 19 years old, was hospitalized for recurrent syncope for 4 days on October 24, 1986. Four days earlier there was palpitation, chest distress, dizziness and weakness without obvious predisposition, a sudden loss of consciousness about half an hour later, , Eyes staring, urinary incontinence, but no vomit foam, wake up after about 2 minutes. 4 days to onset of syncope more than 10 times. Each episode of about 2 to 3 minutes, often induced by the activity. 4 years ago had a similar episode 2 times, and therefore drop out of school. Physical examination: normal blood pressure, consciousness, pupil and other large round, good light reflection. Neck soft, pathology anti-