Abrahams Brett S, Geschwind Daniel H
Neurology Department, and Semel Institute for Neuroscience and Behaviour, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California 90095-1769 USA.
Nat Rev Genet. 2008 May;9(5):341-55. doi: 10.1038/nrg2346.
Autism is a heterogeneous syndrome defined by impairments in three core domains: social interaction, language and range of interests. Recent work has led to the identification of several autism susceptibility genes and an increased appreciation of the contribution of de novo and inherited copy number variation. Promising strategies are also being applied to identify common genetic risk variants. Systems biology approaches, including array-based expression profiling, are poised to provide additional insights into this group of disorders, in which heterogeneity, both genetic and phenotypic, is emerging as a dominant theme.
自闭症是一种异质性综合征,由社交互动、语言和兴趣范围这三个核心领域的损害所定义。最近的研究工作已导致鉴定出多个自闭症易感基因,并使人们对新生和遗传拷贝数变异的作用有了更多认识。还有一些有前景的策略正被用于识别常见的遗传风险变异。包括基于芯片的表达谱分析在内的系统生物学方法,有望为这类疾病提供更多深入见解,在这类疾病中,遗传和表型的异质性正成为一个主要特征。