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新生儿代谢性疾病中的惊厥发作(作者译)

[Convulsive seizures in the neonatal metabolic diseases (author's transl)].

作者信息

Moussalli-Salefranque F, Mises J, Plouin P, Bursztejn M, Ogier H

出版信息

Rev Electroencephalogr Neurophysiol Clin. 1981 Dec;11(3-4):379-84. doi: 10.1016/s0370-4475(81)80074-3.

Abstract

Of 61 newborns with disorders in amino acid metabolism, 20 had seizures; 15 of them have been recorded. Clinically, seizures are mostly partial clonic jerks. There seems to be some homogeneity of EEG features in relation to causal amino acidopathy. In every case where seizures, either electroclinical or only infraclinical, occurred the evolution was very poor, even in those diseases that would have had a good prognosis. Therefore the EEG in the newborns is especially interesting, both as an aid to diagnosis by interictal recording and as a prognostic tool by registration of seizures.

摘要

在61例患有氨基酸代谢紊乱的新生儿中,20例出现惊厥;其中15例已有记录。临床上,惊厥大多为部分性阵挛性抽搐。脑电图特征与病因性氨基酸病之间似乎存在一定的同质性。在每例出现惊厥(无论是临床发作还是仅亚临床发作)的病例中,病情进展都非常差,即使在那些原本预后良好的疾病中也是如此。因此,新生儿脑电图特别值得关注,既有助于通过发作间期记录进行诊断,也有助于通过惊厥记录作为一种预后工具。

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