Department of Biological Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
BMC Med. 2013 May 2;11:119. doi: 10.1186/1741-7015-11-119.
Autism is usually conceptualized as a disorder or disease that involves fundamentally abnormal neurodevelopment. In the present work, the hypothesis that a suite of core autism-related traits may commonly represent simple delays or non-completion of typical childhood developmental trajectories is evaluated.
A comprehensive review of the literature indicates that, with regard to the four phenotypes of (1) restricted interests and repetitive behavior, (2) short-range and long-range structural and functional brain connectivity, (3) global and local visual perception and processing, and (4) the presence of absolute pitch, the differences between autistic individuals and typically developing individuals closely parallel the differences between younger and older children.
The results of this study are concordant with a model of 'developmental heterochrony', and suggest that evolutionary extension of child development along the human lineage has potentiated and structured genetic risk for autism and the expression of autistic perception, cognition and behavior.
自闭症通常被认为是一种涉及神经发育根本异常的障碍或疾病。在本研究中,评估了一套核心自闭症相关特征可能普遍代表典型儿童发育轨迹简单延迟或未完成的假设。
对文献的全面回顾表明,就(1)受限兴趣和重复行为、(2)短程和长程结构和功能脑连接、(3)全局和局部视觉感知和处理以及(4)绝对音高的四种表型而言,自闭症个体与典型发育个体之间的差异与年幼和年长儿童之间的差异密切相关。
本研究的结果与“发育异时性”模型一致,并表明人类谱系中儿童发育的进化延伸增强了自闭症的遗传风险,并表达了自闭症的感知、认知和行为。