Wörle H, Keimer R, Köhler B
Pädiatrisches Zèntrum, Olgahospital, Stuttgart.
Monatsschr Kinderheilkd. 1990 Sep;138(9):615-8.
We present the case report of a girl with a subtype of Lissencephaly syndrome, type I, "Miller-Dieker syndrome", pointing out the specific EEG features in infancy and early childhood. The following pathognomonic EEG manifestations may confirm the diagnosis of an lissencephalic syndrome: abnormally fast background activity of an extraordinary high voltage increasing with age, missing topographic structuring, no reactivity to sleep or medication, unusually high-voltaged sharp-slow-wave complexes.
我们报告了一名患有I型无脑回综合征亚型“米勒-迪克尔综合征”女孩的病例,指出了其在婴儿期和幼儿期的特定脑电图特征。以下具有诊断意义的脑电图表现可确诊无脑回综合征:背景活动异常快速,电压极高,且随年龄增长而增加;缺乏地形结构;对睡眠或药物无反应;出现异常高电压的尖慢波复合波。