[伦诺克斯-加斯东综合征的疾病分类界限（作者译）]

[Nosological limits of the Lennox-Gastaut syndrome (author's transl)].

作者信息

Beaumanoir A

出版信息

Rev Electroencephalogr Neurophysiol Clin. 1981 Dec;11(3-4):468-73. doi: 10.1016/s0370-4475(81)80087-1.

Abstract

Some results of a follow-up study concerning 103 observations of chronic and transitory Lennox-Gastaut syndrome (SLG) are presented. The full-blown syndrome in the chronic SLG (mean duration 21 years and 2 months) is in 100% of the cases characterized by tonic seizures and 'complex absences', mental retardation and abnormal EEG with slow spike-waves and 10 c/sec recruiting bursts. Slow spike-waves are not the most specific EEG pattern of SLG with chronic outcome. The statement is discussed.

摘要

本文介绍了一项关于103例慢性和短暂性Lennox-Gastaut综合征（SLG）观察结果的随访研究。慢性SLG（平均病程21年零2个月）的典型综合征在100%的病例中表现为强直性发作和“复杂失神发作”、智力发育迟缓以及脑电图异常，伴有慢棘波和10次/秒的募集性爆发。慢棘波并非慢性结局的SLG最具特异性的脑电图模式。对这一说法进行了讨论。