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儿童急性脑病性疾病中的获得性可逆性自闭症综合征

Acquired reversible autistic syndrome in acute encephalopathic illness in children.

作者信息

DeLong G R, Bean S C, Brown F R

出版信息

Arch Neurol. 1981 Mar;38(3):191-4. doi: 10.1001/archneur.1981.00510030085013.

Abstract

In seeking the neurologic substrate of the autistic syndrome of childhood, previous studies have implicated the medial temporal lobe or the ring of mesolimbic cortex located in the mesial frontal and temporal lobes. During an acute encephalopathic illness, a clinical picture developed in three children that was consistent with infantile autism. This development was reversible. It was differentiated from acquired epileptic aphasia, and the language disorder was differentiated aphasia. One child has rises in serum herpes simplex titers, and a computerized tomographic (CT) scan revealed an extensive lesion of the temporal lobes, predominantly on the left. The other two, with similar clinical syndromes, had normal CT scans, and no etiologic agent was defined. These cases are examples of an acquired and reversible autistic syndrome in childhood, emphasizing the clinical similarities to bilateral medial temporal lobe disease as described in man, including the Klüver-Bucy syndrome seen in postencephalitic as well as postsurgical states.

摘要

在探寻儿童自闭症综合征的神经学基础时,先前的研究表明内侧颞叶或位于额叶和颞叶内侧的中脑边缘皮质环与之有关。在一次急性脑病发作期间,三名儿童出现了与婴儿自闭症相符的临床表现。这种情况是可逆的。它与获得性癫痫性失语相鉴别,且语言障碍为失语症。一名儿童血清单纯疱疹滴度升高,计算机断层扫描(CT)显示颞叶广泛病变,主要在左侧。另外两名有类似临床综合征的儿童CT扫描正常,且未明确病因。这些病例是儿童获得性和可逆性自闭症综合征的实例,强调了与人类双侧内侧颞叶疾病的临床相似性,包括在脑炎后以及手术后状态中出现的克吕弗-布西综合征。

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