Newbury Dianne F, Bishop Dorothy V M, Monaco Anthony P
Wellcome Trust Centre for Human Genetics, Oxford University, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK.
Trends Cogn Sci. 2005 Nov;9(11):528-34. doi: 10.1016/j.tics.2005.09.002. Epub 2005 Sep 26.
It has been known for some years that specific language impairment (SLI), an unexpected failure to acquire age-appropriate language skills, is highly heritable. However, molecular genetic studies have been hampered by the heterogeneity of the disorder and the predominant lack of clear genotype-phenotype relationships. We review recent studies suggesting that a better understanding of the genetics of SLI might emerge if we move away from clinical criteria for diagnosis to look instead at a theoretically based quantitative and cognitive measure of the phenotype: a test of phonological short-term memory (STM). Deficient phonological STM has been linked to specific genetic loci, and might play a role in determining some types of reading impairment as well as SLI. Identifying those cognitive deficits that work best as indices of heritable phenotypes will help us to uncover the aetiology of developmental disorders.
多年来人们已经知道,特定语言障碍(SLI),即意外无法获得适合其年龄的语言技能,具有高度遗传性。然而,分子遗传学研究一直受到该疾病异质性的阻碍,并且主要缺乏明确的基因型 - 表型关系。我们回顾了最近的研究,这些研究表明,如果我们从临床诊断标准转向基于理论的对表型的定量和认知测量:语音短期记忆(STM)测试,那么可能会更好地理解SLI的遗传学。语音STM缺陷已与特定基因座相关联,并且可能在确定某些类型的阅读障碍以及SLI中起作用。确定那些最能作为可遗传表型指标的认知缺陷将有助于我们揭示发育障碍的病因。