Haas R H, Townsend J, Courchesne E, Lincoln A J, Schreibman L, Yeung-Courchesne R
Department of Neurosciences, University of California San Diego, La Jolla, USA.
J Child Neurol. 1996 Mar;11(2):84-92. doi: 10.1177/088307389601100204.
Neuroanatomic, pathologic, and neurobehavioral studies point to a cerebellar and parietal abnormality in autism. We used a standardized protocol to examine neurologic function in 28 pediatric autistic subjects and 24 pediatric normal healthy volunteer controls. As a group, the autistic subjects had quantitative measures from magnetic resonance imaging suggesting hypoplasia or hyperplasia of the cerebellar vermis, as well as measurements of posterior corpus callosum suggesting abnormalities of posterior cortex. In groups of tests that reflect cerebellar and parietal function, the neurologic abnormalities detectable by clinical examination were significantly greater for autistic subjects than for normal controls. These studies confirm that the structural and behavioral deficit in autism does lead to abnormalities that can be detected on the clinical neurologic examination.
神经解剖学、病理学和神经行为学研究表明,自闭症患者存在小脑和顶叶异常。我们采用标准化方案,对28名自闭症儿童受试者和24名正常健康儿童志愿者对照进行神经功能检查。作为一个群体,自闭症受试者的磁共振成像定量测量结果显示,小脑蚓部存在发育不全或增生,同时胼胝体后部测量结果表明后皮质存在异常。在反映小脑和顶叶功能的测试组中,临床检查可检测到的自闭症受试者神经异常明显多于正常对照组。这些研究证实,自闭症的结构和行为缺陷确实会导致临床神经检查中可检测到的异常。