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[肌阵挛-无动性小发作状态的鉴别诊断困难]

[Differential diagnostic difficulties in myoclonic-astatic petit mal status].

作者信息

Müller J, Müller D

出版信息

Schweiz Arch Neurol Neurochir Psychiatr. 1975;117(2):241-54.

PMID:817392
Abstract

Myoclonic-astatic attack syndromes tend more than other attack forms to produce states. Their clinical picture can be various and therefore cause differential-diagnostic difficulties. On four own examples they are referred to. Most frequently it will be necessary to differentiate the hardly adjustable attack syndrome from on overdose of anticonvulsives. Also the state of absences, the state of psychomotoric attacks, and the impulsive-petit-mal state can make differential-diagnostic difficulties. Furthermore, additional encephalitic processes with cerebral decompensation in anyway injured children, and the myoclonic variants of familial amaurotic idiocy are to be to consider. An EEG examination is indispensable; consideration of the total situtation, observation of the course, and recording of the actual findings are necessary.

摘要

肌阵挛-无动性发作综合征比其他发作形式更容易引发各种状态。其临床表现可能多种多样,因此会导致鉴别诊断困难。文中列举了四个自身病例。最常见的情况是,需要将难以控制的发作综合征与抗惊厥药物过量引起的情况进行鉴别。失神状态、精神运动性发作状态以及冲动性小发作状态也可能造成鉴别诊断困难。此外,对于任何脑部受损儿童出现的伴有脑功能失代偿的额外脑炎过程,以及家族性黑蒙性白痴的肌阵挛变体也需要加以考虑。脑电图检查必不可少;必须综合考虑整体情况、观察病程并记录实际检查结果。

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