Watanabe K, Hara K, Iwase K
Neuropadiatrie. 1976 Feb;7(1):19-41. doi: 10.1055/s-0028-1091608.
The evolution of EEG, visual and auditory evoked responses (VER and AER) and sleep is described in three cases of semilobar holoprosencephaly. During the neonatal period, the waking EEG was characterized by almost continuous high amplitude rhythmic alpha-theta activity in case 1 and 2, which became discontinuous during quiet sleep. Moderate amplitude rhythmic alpha-theta waves were seen in case 3. This rhythmic alpha-theta activity gradually disappeared with increasing age, being replaced by non-specific slow dysrhythmia. In case 3, the subsequent EEGs were characterized by focal spikes at 4 months, multifocal spikes at 5 and 6 months, hypsarrhythmia at 8 months and bisynchronous diffuse sharp and slow wave discharges at 2 years and 7 months. Ictal EEGs were characterized by desynchronization and/or rapid synchronization, epileptic recruiting rhythm and postical high amplitude slow waves. Definite but mostly abnormal VERs or AERs were obtained in all three cases. In two cases, the evoked responses showed a progressive decrease in amplitude and VERs were abolished finally. No sleep cycle could be identified during the neonatal period probably because of frequent seizures. In two cases no circadian rhythm of sleep developed, although almost normal REM-NREM sleep cycle was present.
本文描述了3例半叶型前脑无裂畸形患者脑电图(EEG)、视觉诱发电位(VER)和听觉诱发电位(AER)以及睡眠的演变情况。在新生儿期,病例1和病例2清醒时的脑电图特征为几乎持续的高波幅节律性α-θ活动,安静睡眠时变为间断性。病例3可见中等波幅的节律性α-θ波。随着年龄增长,这种节律性α-θ活动逐渐消失,被非特异性慢节律紊乱所取代。病例3随后的脑电图特征为4个月时出现局灶性棘波,5个月和6个月时出现多灶性棘波,8个月时出现高度失律,2岁7个月时出现双同步弥漫性尖慢波发放。发作期脑电图特征为去同步化和/或快速同步化、癫痫募集节律以及发作后高波幅慢波。所有3例均获得明确但大多异常的VER或AER。2例中,诱发电位的波幅逐渐降低,最终VER消失。新生儿期可能因频繁发作而无法识别睡眠周期。2例中虽存在几乎正常的快速眼动睡眠-非快速眼动睡眠周期,但未形成昼夜睡眠节律。