Lagenstein I, Sternowsky H J, Koepp P, Leiber U
Klin Padiatr. 1978 Sep;190(5):507-11.
EEG findings and the course of epileptic seizures in two patients with neuronal ceroid lipofuscinosis (Batten Spielmeyer Vogt syndrome) are presented. Both patients, during the course of disease, developed therapy resistant epileptic reactions with myoclonicastatic seizures. These seizures in connection with diffuse encephalopathy and EEG pattern with 2.5 to 3.5/sec slow-spike-wave meet the criteria of the Lennox syndrome. Pathogenetic questions regarding possible additional genetic predisposition for epileptic seizures are discussed. Since therapeutic effect of different medications is uncertain hormonal therapy may be considered.
本文介绍了两名患有神经元蜡样脂褐质沉积症(巴滕 - 施皮尔曼 - 沃格特综合征)患者的脑电图(EEG)检查结果及癫痫发作病程。两名患者在疾病过程中均出现了对治疗耐药的癫痫反应,并伴有肌阵挛 - 静止性发作。这些发作与弥漫性脑病以及2.5至3.5次/秒慢棘波的脑电图模式符合伦诺克斯综合征的标准。文中讨论了关于癫痫发作可能存在的额外遗传易感性的发病机制问题。由于不同药物的治疗效果不确定,可考虑激素治疗。