Department of Psychology, American University, 4400 Massachusetts Ave NW, Washington, DC 20016, USA.
Cerebellum. 2013 Apr;12(2):267-76. doi: 10.1007/s12311-012-0407-1.
Developmental dyslexia is a genetically based neurobiological syndrome, which is characterized by reading difficulty despite normal or high general intelligence. Even remediated dyslexic readers rarely achieve fast, fluent reading. Some dyslexics also have impairments in attention, short-term memory, sequencing (letters, word sounds, and motor acts), eye movements, poor balance, and general clumsiness. The presence of "cerebellar" motor and fluency symptoms led to the proposal that cerebellar dysfunction contributes to the etiology of dyslexia. Supporting this, functional imaging studies suggest that the cerebellum is part of the neural network supporting reading in typically developing readers, and reading difficulties have been reported in patients with cerebellar damage. Differences in both cerebellar asymmetry and gray matter volume are some of the most consistent structural brain findings in dyslexics compared with good readers. Furthermore, cerebellar functional activation patterns during reading and motor learning can differ in dyslexic readers. Behaviorally, some children and adults with dyslexia show poorer performance on cerebellar motor tasks, including eye movement control, postural stability, and implicit motor learning. However, many dyslexics do not have cerebellar signs, many cerebellar patients do not have reading problems, and differences in dyslexic brains are found throughout the whole reading network, and not isolated to the cerebellum. Therefore, impaired cerebellar function is probably not the primary cause of dyslexia, but rather a more fundamental neurodevelopmental abnormality leads to differences throughout the reading network.
发展性阅读障碍是一种基于遗传的神经生物学综合征,其特征是阅读困难,尽管一般智力正常或较高。即使经过矫正,阅读障碍者也很少能实现快速、流畅的阅读。一些阅读障碍者还存在注意力、短期记忆、排序(字母、单词发音和运动行为)、眼球运动、平衡不良和一般笨拙等问题。“小脑”运动和流畅性症状的存在导致了小脑功能障碍可能导致阅读障碍的病因的假设。支持这一观点的是,功能成像研究表明,小脑是支持典型发育读者阅读的神经网络的一部分,并且已经报道小脑损伤的患者存在阅读困难。与优秀读者相比,阅读障碍者的小脑不对称和灰质体积差异是最一致的结构性脑发现之一。此外,阅读障碍者在阅读和运动学习期间的小脑功能激活模式可能存在差异。行为上,一些阅读障碍儿童和成人在小脑运动任务(包括眼球运动控制、姿势稳定性和内隐运动学习)上表现较差。然而,许多阅读障碍者没有小脑迹象,许多小脑患者没有阅读问题,并且阅读障碍者大脑的差异存在于整个阅读网络中,而不仅仅局限于小脑。因此,小脑功能障碍可能不是阅读障碍的主要原因,而是更基本的神经发育异常导致了整个阅读网络的差异。