Kaddurah Ahmad K, Holmes Gregory L
Hurley Medical Center, Flint, Michigan, USA.
Pediatr Neurol. 2009 May;40(5):343-6. doi: 10.1016/j.pediatrneurol.2008.11.011.
Benign neonatal sleep myoclonus is a condition characterized by myoclonus occurring during sleep. Reported here are 18 cases of infants who had electroencephalographic monitoring, with myoclonic events recorded in 17 cases. In all cases, onset was within days to a few weeks of birth. In no case was the diagnosis of sleep myoclonus considered by the referring primary care physician. Myoclonus was evident during sleep in all 18 infants, but in two of them it was observed also during the transition from sleep to awakening. The behavioral features of the disorder were more varied than previously described: four of the infants had lateralized myoclonus and two had myoclonus involving the head and face. In most of the children, the duration of myoclonus was brief, but in two cases the paroxysmal events lasted more than 30 minutes. None of the children had electroencephalographic abnormalities during the myoclonus. The condition was short-lived, with the myoclonus resolving in most children within 3 months of onset. Benign neonatal sleep myoclonus is an under-recognized condition but one that has a consistently favorable outcome. Infants with the condition should not be treated with antiepileptic drugs.
良性新生儿睡眠肌阵挛是一种以睡眠期间出现肌阵挛为特征的病症。本文报告了18例接受脑电图监测的婴儿,其中17例记录到肌阵挛事件。所有病例的发病均在出生后数天至几周内。转诊的初级保健医生均未考虑诊断为睡眠肌阵挛。18例婴儿在睡眠期间肌阵挛均很明显,但其中2例在从睡眠过渡到觉醒时也观察到肌阵挛。该病症的行为特征比先前描述的更多样化:4例婴儿有单侧肌阵挛,2例有涉及头部和面部的肌阵挛。大多数儿童的肌阵挛持续时间较短,但有2例阵发性事件持续超过30分钟。所有儿童在肌阵挛期间脑电图均无异常。该病症持续时间较短,大多数儿童的肌阵挛在发病后3个月内消失。良性新生儿睡眠肌阵挛是一种未得到充分认识的病症,但预后始终良好。患有该病症的婴儿不应使用抗癫痫药物治疗。