Doose H, Gerken H, Koenig G, Völzke E
Neuropadiatrie. 1978 May;9(2):140-56. doi: 10.1055/s-0028-1085419.
Report of follow-up studies in 65 children with occipital slow rhythms in the EEG (287 records). Two types of occipital rhythms can be differentiated: Paroxysmal bursts of 3--4/s-rhythms with high amplitude (I) accentuated by closing eyes and continuous usually regular occipital 3--4/s-rhythms (II). Type I is identical with the sinusoidal occipital 3/s-rhythms, which are observed especially frequently in childhood epilepsies. It could be demonstrated by follow-up studies, that the phenomenon usually disappears at latest during puberty. --The second type may also disappear during puberty or may even persist until the adult age. This persisting type is identical with what is quoted as "Grundrhythmusvariante" in the German literature. The continuous occipital rhythms could be demonstrated at earliest at age 3. The rhythms change their shape, amplitude, frequency and localisation during growth: In children prior to age 10 the rhythms show more often occipital accentuation in monopolar leads (against ear as reference); the amplitudes are higher on average; the frequency is often less than 4/s, and alpha groups preceding the rhythms after closing the eyes are less pronounced than in older children. Subharmonic waves are frequent. In the same manner as in adults a mostly right sided lateralisation can be seen. Genetic factors may be involved in the development of the occipital rhythms, although a simple mendelian transmission could not be confirmed. The EEG phenomenon is correlated with symptoms of psychic and vegetative lability. There is no correlation to epilepsy. The high incidence of anamnestic risk factors suggests that exogenous factors are at least contributing to the development of the rhythms. The continuous occipital 3--4/s-rhythms must be understood as the symptom of a disturbed development of central pacemaker systems. It can lead to persisting abnormalities or only occur transitorily in certain stages of the brain maturation.
65例脑电图显示枕区慢节律儿童的随访研究报告(287份记录)。枕区节律可分为两种类型:闭眼时增强的3 - 4次/秒高波幅阵发性爆发(I型)和通常规则的持续性枕区3 - 4次/秒节律(II型)。I型与枕区3次/秒正弦节律相同,在儿童癫痫中尤为常见。随访研究表明,这种现象通常最迟在青春期消失。——第二种类型也可能在青春期消失,甚至可能持续到成年。这种持续存在的类型与德国文献中引用的“基本节律变体”相同。持续性枕区节律最早在3岁时可被检测到。在生长过程中,节律的形态、波幅、频率和定位会发生变化:10岁以前的儿童,单极导联(以对耳为参考)中枕区增强更为常见;平均波幅更高;频率通常低于4次/秒,闭眼后节律之前的α波群不如年长儿童明显。谐波常见。与成人一样,大多可见右侧优势。遗传因素可能参与枕区节律的发育,尽管未能证实简单的孟德尔遗传传递。脑电图现象与精神和植物神经不稳定症状相关。与癫痫无关。既往危险因素的高发生率表明外源性因素至少对节律的发展有影响。持续性枕区3 - 4次/秒节律必须被理解为中枢起搏器系统发育紊乱的症状。它可能导致持续异常,或仅在大脑成熟的某些阶段短暂出现。