Olsson I, Hedström A
Department of Paediatrics II, Gothenburg University, Sweden.
Acta Paediatr Scand. 1991 Feb;80(2):235-42. doi: 10.1111/j.1651-2227.1991.tb11839.x.
A population-based study of absence epilepsy in Swedish children, aged 0-15 years, comprised cases selected on the basis of EEG criteria. Absence epilepsy was found in 119 of the 134 children with 3 Hz spike-and-wave discharges, and 12 of these 119 (10.1%) had typical absences in addition to other generalized seizures and slow irregular spike-and-wave activity on the EEG. The mean annual incidence of this type of absence epilepsy was 0.7/100,000. The median age at onset of absences was 6 years. Eight of the 12 patients had neurological abnormalities and/or severe mental retardation. The patients constitute a heterogeneous group of encephalopathies. They may have a genetic predisposition for absence epilepsy, causing it to appear during the course of a more severe, encephalopathy related, type of epilepsy.
一项针对瑞典0至15岁儿童失神癫痫的基于人群的研究,纳入了根据脑电图标准选取的病例。在134例有3赫兹棘慢波放电的儿童中,发现119例患有失神癫痫,这119例中的12例(10.1%)除了其他全身性癫痫发作外,还伴有典型失神发作,且脑电图上有缓慢不规则棘慢波活动。这种类型的失神癫痫的年平均发病率为0.7/10万。失神发作的中位发病年龄为6岁。12例患者中有8例存在神经功能异常和/或严重智力障碍。这些患者构成了一组异质性脑病。他们可能存在失神癫痫的遗传易感性,导致其在更严重的、与脑病相关的癫痫病程中出现。