儿童孤独症的遗传学研究进展
Chinese Journal of Maternal and Child Health Research(2008)
Abstract
儿童孤独症是一种起病于婴幼儿时期的严重发育障碍性疾病,临床主要表现为社会交往障碍、语言交流障碍和兴趣范围狭窄、重复或刻板运动的综合征,目前被认为是多因素、多基因遗传性疾病,但与其相关的基因尚未明确.文章从遗传学的几个方面进行论述,着重介绍与孤独症显著相关的候选基因.
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Key words
genetics,gene,autism,children
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