Horn C A, Beekman R H, Dick M, Lacina S J
Am J Dis Child. 1986 Jul;140(7):659-61. doi: 10.1001/archpedi.1986.02140210057025.
The congenital long QT syndrome is an unusual disorder characterized by Q-T interval prolongation on electrocardiogram that predisposes the heart to ventricular tachycardia and fibrillation. We describe herein four patients with the congenital long QT syndrome who initially presented with generalized seizures. Three of these children were initially misdiagnosed as having a primary seizure disorder. The causal relationship of complex ventricular arrhythmias to seizure activity was documented in each child. This experience emphasizes the importance of obtaining an electrocardiogram in all children with a seizure disorder of unknown origin.
先天性长QT综合征是一种罕见的疾病,其特征是心电图上Q-T间期延长,使心脏易发生室性心动过速和颤动。我们在此描述了4例先天性长QT综合征患者,他们最初表现为全身性癫痫发作。其中3名儿童最初被误诊为原发性癫痫障碍。在每个儿童中都记录了复杂室性心律失常与癫痫活动之间的因果关系。这一经验强调了对所有不明原因癫痫障碍儿童进行心电图检查的重要性。