Bauer J, Elger C E
Department of Epileptology, University of Bonn, Germany.
Seizure. 1994 Jun;3(2):153-5. doi: 10.1016/s1059-1311(05)80207-9.
Neuronal migration disorders are rare malformations which can be associated with epileptic seizures. We report about a 14-year-old female patient suffering from epilepsy with infantile spasms, myoclonic-astatic seizures and absences. The EEG showed generalized 2.5-3/sec spike-wave paroxysms. As the possible cause of the disease the MRI scan exhibited a bilateral band heterotopia.
神经元迁移障碍是一种罕见的畸形，可伴有癫痫发作。我们报告了一名14岁的女性患者，患有癫痫，伴有婴儿痉挛、肌阵挛-站立不能发作和失神发作。脑电图显示广泛性2.5-3次/秒的棘慢波阵发。作为该疾病的可能病因，磁共振成像扫描显示双侧带状灰质异位。
