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与语言障碍相关的遗传风险因素。

Heritable risk factors associated with language impairments.

作者信息

Barry J G, Yasin I, Bishop D V M

机构信息

Department of Experimental Psychology, University of Oxford, South Parks Road, Oxford, UK.

出版信息

Genes Brain Behav. 2007 Feb;6(1):66-76. doi: 10.1111/j.1601-183X.2006.00232.x.

DOI:10.1111/j.1601-183X.2006.00232.x
PMID:17233642
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1974814/
Abstract

There is a strong genetic contribution to children's language and literacy impairments. The aim of this study was to determine which aspects of the phenotype are familial by comparing 34 parents of probands with language/literacy impairments and 33 parents of typically developing probands. The parents responded to questionnaires regarding previous history for language/reading impairment and participated in psychometric testing. The psychometric test battery consisted of tests assessing non-verbal IQ, short-term memory, articulation, receptive grammar, reading abilities and spelling. Self-report measures demonstrated a higher prevalence of language and literacy impairments in parents of affected probands (32%) compared with parents of unaffected probands (6%). The two groups of parents differed significantly in their performance on the non-word repetition, oromotor and digit span tasks. Non-word repetition gave the best discrimination between the parent groups even when the data from the parents who actually were impaired as ascertained by direct testing or self-report were removed from the analyses. This suggests that non-word repetition serves as a marker of a family risk for language impairment. The paper concludes with a discussion of issues associated with ascertainment of specific language impairment (SLI).

摘要

儿童的语言和读写障碍有很强的遗传因素。本研究的目的是通过比较34名患有语言/读写障碍先证者的父母和33名发育正常先证者的父母,来确定该表型的哪些方面具有家族性。父母们回答了有关语言/阅读障碍既往史的问卷,并参加了心理测量测试。心理测量测试组包括评估非语言智商、短期记忆、发音、接受性语法、阅读能力和拼写的测试。自我报告测量显示,与未受影响先证者的父母(6%)相比,受影响先证者的父母中语言和读写障碍的患病率更高(32%)。两组父母在非单词重复、口面部运动和数字广度任务中的表现存在显著差异。即使将通过直接测试或自我报告确定实际受损的父母的数据从分析中剔除,非单词重复在区分父母组方面表现最佳。这表明非单词重复可作为语言障碍家族风险的一个指标。本文最后讨论了与特定语言障碍(SLI)确诊相关的问题。

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本文引用的文献

1
Is dyslexia a form of specific language impairment? A comparison of dyslexic and language impaired children as adolescents.诵读困难是否为一种特定语言障碍?以青少年为例对诵读困难儿童和语言障碍儿童的比较。
Ann Dyslexia. 2000 Jan;50(1):103-20. doi: 10.1007/s11881-000-0019-1.
2
Estimating familial loading in SLI: a comparison of direct assessment versus parental interview.估计特定语言障碍中的家族负荷:直接评估与父母访谈的比较。
J Speech Lang Hear Res. 2006 Feb;49(1):88-101. doi: 10.1044/1092-4388(2006/007).
3
Are specific language impairment and dyslexia distinct disorders?特定语言障碍和诵读困难是不同的疾病吗?
J Speech Lang Hear Res. 2005 Dec;48(6):1378-96. doi: 10.1044/1092-4388(2005/096).
4
Are phonological processing deficits part of the broad autism phenotype?语音处理缺陷是广泛自闭症表型的一部分吗?
Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):54-60. doi: 10.1002/ajmg.b.30039.
5
Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment.在受特定语言障碍影响的个体扩大样本中,与SLI1基因座存在高度显著的连锁关系。
Am J Hum Genet. 2004 Jun;74(6):1225-38. doi: 10.1086/421529. Epub 2004 May 3.
6
Family pedigrees of children with suspected childhood apraxia of speech.疑似儿童言语失用症患儿的家系图谱。
J Commun Disord. 2004 Mar-Apr;37(2):157-75. doi: 10.1016/j.jcomdis.2003.08.003.
7
Identifying neurocognitive phenotypes in autism.识别自闭症中的神经认知表型。
Philos Trans R Soc Lond B Biol Sci. 2003 Feb 28;358(1430):303-14. doi: 10.1098/rstb.2002.1198.
8
Sensitivity to word order cues by normal and language/learning disabled adults.正常成年人与语言/学习障碍成年人对词序线索的敏感度。
J Commun Disord. 2002 Sep-Oct;35(5):453-62. doi: 10.1016/s0021-9924(02)00094-1.
9
The role of genes in the etiology of specific language impairment.基因在特定语言障碍病因学中的作用。
J Commun Disord. 2002 Jul-Aug;35(4):311-28. doi: 10.1016/s0021-9924(02)00087-4.
10
A genomewide scan identifies two novel loci involved in specific language impairment.一项全基因组扫描鉴定出两个与特定语言障碍相关的新基因座。
Am J Hum Genet. 2002 Feb;70(2):384-98. doi: 10.1086/338649. Epub 2002 Jan 4.