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自闭症中小脑蚓部小叶VI和VII发育不全。

Hypoplasia of cerebellar vermal lobules VI and VII in autism.

作者信息

Courchesne E, Yeung-Courchesne R, Press G A, Hesselink J R, Jernigan T L

机构信息

Neuropsychology Research Laboratory, Children's Hospital Research Center, San Diego, Calif. 92123.

出版信息

N Engl J Med. 1988 May 26;318(21):1349-54. doi: 10.1056/NEJM198805263182102.

Abstract

Autism is a neurologic disorder that severely impairs social, language, and cognitive development. Whether autism involves maldevelopment of neuroanatomical structures is not known. The size of the cerebellar vermis in patients with autism was measured on magnetic resonance scans and compared with its size in controls. The neocerebellar vermal lobules VI and VII were found to be significantly smaller in the patients. This appeared to be a result of developmental hypoplasia rather than shrinkage or deterioration after full development had been achieved. In contrast, the adjacent vermal lobules I to V, which are ontogenetically, developmentally, and anatomically distinct from lobules VI and VII, were found to be of normal size. Maldevelopment of the vermal neocerebellum had occurred in both retarded and nonretarded patients with autism. This localized maldevelopment may serve as a temporal marker to identify the events that damage the brain in autism, as well as other neural structures that may be concomitantly damaged. Our findings suggest that in patients with autism, neocerebellar abnormality may directly impair cognitive functions that some investigators have attributed to the neocerebellum; may indirectly affect, through its connections to the brain stem, hypothalamus, and thalamus, the development and functioning of one or more systems involved in cognitive, sensory, autonomic, and motor activities; or may occur concomitantly with damage to other neural sites whose dysfunction directly underlies the cognitive deficits in autism.

摘要

自闭症是一种严重损害社交、语言和认知发展的神经障碍。自闭症是否涉及神经解剖结构发育异常尚不清楚。通过磁共振扫描测量了自闭症患者小脑蚓部的大小,并与对照组的大小进行了比较。发现自闭症患者的新小脑蚓部小叶VI和VII明显较小。这似乎是发育不全的结果,而不是在完全发育后出现萎缩或退化。相比之下,在个体发生、发育和解剖学上与小叶VI和VII不同的相邻蚓部小叶I至V,其大小正常。自闭症患者无论是智力发育迟缓还是正常,均出现了新小脑蚓部发育异常。这种局部发育异常可能作为一个时间标记,来识别自闭症中损害大脑的事件,以及可能同时受损的其他神经结构。我们的研究结果表明,在自闭症患者中,新小脑异常可能直接损害一些研究人员归因于新小脑的认知功能;可能通过其与脑干、下丘脑和丘脑的连接,间接影响参与认知、感觉、自主和运动活动的一个或多个系统的发育和功能;或者可能与其他神经部位的损伤同时发生,这些部位的功能障碍直接导致了自闭症的认知缺陷。

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