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越来越离奇了:皮质特化的遗传障碍。

Curiouser and curiouser: genetic disorders of cortical specialization.

机构信息

Smurfit Institute of Genetic and Institute of Neuroscience, Trinity College Dublin, Dublin 2, Ireland.

出版信息

Curr Opin Genet Dev. 2011 Jun;21(3):271-7. doi: 10.1016/j.gde.2010.12.003. Epub 2011 Feb 4.

Abstract

The processes by which cortical areas become specialized for high-level cognitive functions may be revealed by the study of familial developmental disorders such as dyslexia, dyscalculia, prosopagnosia, color agnosia and amusia. These disorders are characterised by the inability to integrate information across multiple areas and the consequent failure to develop representations of the knowledge of some category based on its associated attributes. In contrast, synesthesia may be seen as a hyper-associative condition, possibly due to a failure to properly segregate areas into distinct networks. Here, I consider recent advances in our understanding of the genetic and neurobiological bases of these conditions and the developmental mechanisms underlying the specialization of cortical areas and networks.

摘要

通过研究家族性发育障碍,如阅读障碍、计算障碍、面孔失认症、颜色失认症和失乐症,我们可以揭示大脑皮质区域专门化用于高级认知功能的过程。这些障碍的特征是无法跨多个区域整合信息,因此无法根据某些类别的相关属性来发展其知识表示。相比之下,联觉可能被视为一种超联想状态,这可能是由于未能将区域正确地划分为不同的网络。在这里,我考虑了我们对这些疾病的遗传和神经生物学基础以及大脑皮质区域和网络专门化的发育机制的最新理解的进展。

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