先天性兰伯特-伊顿肌无力综合征
Congenital Lambert-Eaton myasthenic syndrome.
作者信息
Bady B, Chauplannaz G, Carrier H
出版信息
J Neurol Neurosurg Psychiatry. 1987 Apr;50(4):476-8. doi: 10.1136/jnnp.50.4.476.
Abstract
A 4 year old girl had been hypotonic and areflexic since birth with delayed milestones in motor development. Repetitive stimulation at high rates performed at 3 years elicited an incremental response typical of the Lambert-Eaton Syndrome.
摘要
一名4岁女孩自出生以来就表现为肌张力减退和反射消失，运动发育里程碑延迟。3岁时进行的高频重复刺激引发了典型的兰伯特-伊顿综合征递增反应。
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