Haga Y, Watanabe K, Negoro T, Aso K, Kasai K, Ohki T, Natume J
Department of Pediatrics; Nagoya University School of Medicine, Japan.
Pediatr Neurol. 1995 Oct;13(3):226-9. doi: 10.1016/0887-8994(95)00157-b.
Ictal electroencephalographic/video recordings of 42 patients with West syndrome (WS) were reviewed to define the relation between ictal, clinical, and EEG features and etiology or prognosis. The duration and type of spasms, the number of spasms per cluster, and the interval between spasms did not correlate with the etiology or the short-term prognosis. However, eye deviation, asymmetric spasms, and partial seizures concomitant with spasms were observed only in symptomatic WS patients with poor outcome. In particular, all 8 patients with concurrent partial seizures had severe psychomotor retardation. The ictal EEG characteristics did not correlate with etiology and prognosis. There was no significant difference between the patients with persistence or reappearance of hypsarrhythmia and the patients without interspasm hypsarrhythmia.
回顾了42例韦斯特综合征(WS)患者的发作期脑电图/视频记录,以确定发作期、临床和脑电图特征与病因或预后之间的关系。痉挛的持续时间和类型、每簇痉挛的次数以及痉挛之间的间隔与病因或短期预后均无相关性。然而,仅在预后不良的症状性WS患者中观察到眼球偏斜、不对称痉挛以及与痉挛同时出现的部分性发作。特别是,所有8例并发部分性发作的患者均有严重的精神运动发育迟缓。发作期脑电图特征与病因和预后无关。高峰失律持续或再现的患者与无痉挛间期高峰失律的患者之间无显著差异。