Meierkord H, Fish D R, Smith S J, Scott C A, Shorvon S D, Marsden C D
University Department of Clinical Neurology, Institute of Neurology, London, England.
Mov Disord. 1992;7(1):38-42. doi: 10.1002/mds.870070107.
The sex ratio, age at onset, and ictal features of nine patients with nocturnal paroxysmal dystonia were compared with those of eight patients with daytime frontal lobe seizures and eight patients with nocturnal motor attacks of known epileptic origin. All patients underwent video electroencephalography telemetry. There were no clinical features that would allow distinction between the groups and no single phenomenon was uniquely seen in nocturnal paroxysmal dystonia. This study provides no evidence that nocturnal paroxysmal dystonia is a separate diagnostic entity.
将9例夜间阵发性肌张力障碍患者的性别比例、发病年龄和发作期特征与8例日间额叶癫痫患者及8例已知癫痫起源的夜间运动发作患者进行了比较。所有患者均接受了视频脑电图遥测。没有临床特征可用于区分这些组,且在夜间阵发性肌张力障碍中未独特地观察到单一现象。本研究没有提供证据表明夜间阵发性肌张力障碍是一个独立的诊断实体。