Suppr超能文献

从基因到发育性阅读障碍中的行为表现

From genes to behavior in developmental dyslexia.

作者信息

Galaburda Albert M, LoTurco Joseph, Ramus Franck, Fitch R Holly, Rosen Glenn D

机构信息

Department of Neurology, Division of Behavioral Neurology, Harvard Medical School, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215, USA.

出版信息

Nat Neurosci. 2006 Oct;9(10):1213-7. doi: 10.1038/nn1772.

Abstract

All four genes thus far linked to developmental dyslexia participate in brain development, and abnormalities in brain development are increasingly reported in dyslexia. Comparable abnormalities induced in young rodent brains cause auditory and cognitive deficits, underscoring the potential relevance of these brain changes to dyslexia. Our perspective on dyslexia is that some of the brain changes cause phonological processing abnormalities as well as auditory processing abnormalities; the latter, we speculate, resolve in a proportion of individuals during development, but contribute early on to the phonological disorder in dyslexia. Thus, we propose a tentative pathway between a genetic effect, developmental brain changes, and perceptual and cognitive deficits associated with dyslexia.

摘要

迄今为止,所有与发育性阅读障碍相关的四个基因都参与大脑发育,并且越来越多的研究报道了阅读障碍患者存在大脑发育异常。在幼年啮齿动物大脑中诱发的类似异常会导致听觉和认知缺陷,这突出了这些大脑变化与阅读障碍之间的潜在关联。我们对阅读障碍的看法是,一些大脑变化会导致语音处理异常以及听觉处理异常;我们推测,后者在一部分个体的发育过程中会得到解决,但在早期会导致阅读障碍中的语音障碍。因此,我们提出了一条从基因效应、大脑发育变化到与阅读障碍相关的感知和认知缺陷的初步途径。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验