Department of Paediatric Neurology, Evelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Mov Disord. 2010 Feb 15;25(3):385-9. doi: 10.1002/mds.22926.
In Rett syndrome (RS), acute life-threatening episodes (ALTEs) are usually attributed to epilepsy or autonomic dysfunction but they can represent a movement disorder (MD). We describe three girls with RS who experienced ALTEs from an early age. These were long considered epileptic until video-EEG in Patients 1 and 3 revealed their non-epileptic nature. A primary dystonic mechanism was suspected and Patients 1 and 2 were treated with Trihexyphenidyl with significantly reduced frequency of the ALTEs. Patient 3 died before Trihexyphenidyl was tried. Trihexyphenidyl in RS patients with similar presentations can modify the dystonia and prevent ALTEs.
在雷特综合征(RS)中,急性危及生命的发作(ALTEs)通常归因于癫痫或自主功能障碍,但它们可能代表运动障碍(MD)。我们描述了三个患有 RS 的女孩,她们从很小的时候就经历了 ALTEs。这些在很长一段时间内都被认为是癫痫发作,直到患者 1 和 3 的视频脑电图显示出它们的非癫痫性质。怀疑存在原发性肌张力障碍机制,患者 1 和 2 接受了三己酚汀治疗,ALTE 的发作频率明显降低。患者 3 在尝试三己酚汀之前死亡。RS 患者中出现类似表现的三己酚汀可改善肌张力障碍并预防 ALTEs。