Genetic studies of specific language impairment (SLI) using consanguineousfamilies
Genetic studies of specific language impairment (SLI) using consanguineousfamilies
批准号:
10378769
负责人:
Muhammad Hashim Raza
金额:
$14.63万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-04-10 至 2024-03-31
关键词:
AcuteAffectAgeAllelesAttentionCandidate Disease GeneChildChromosome MappingClinicalCommunicationComplexDevelopmentDevelopmental Delay DisordersDiagnosisDigit structureDiseaseEnrollmentExtended FamilyFamilyFamily StudyFamily memberFrequenciesGene ExpressionGenesGeneticGenetic DiseasesGenetic StatusGenetic studyGoalsHearing problemHeritabilityHomoIndividualIntellectual functioning disabilityInvestigationLanguageLearningLifeMapsMeasuresMental RetardationMethodsMolecularNational Institute on Deafness and Other Communication DisordersNatureNeurodevelopmental DisorderNuclear FamilyOther GeneticsOutcomePakistanPathway interactionsPerformancePhenotypePilot ProjectsPopulationPopulation ControlPrevalenceQuestionnairesRecording of previous eventsReportingResearchSalvelinusSamplingSchoolsShort-Term MemorySpeechSpeech DisordersStutteringSuggestionTranslatingTwin StudiesUnited StatesVocabulary Testaffectionautism spectrum disorderbasecase controlcohortconsanguineous familydevelopmental diseasedisease classificationexome sequencinggenetic analysisgenetic pedigreegenetic variantgenome wide association studygenome-widegenomic locushearing impairmenthereditary hearing lossimprovedmutantnovelpeerrare variantrecruitrisk variantscreeningskillssocialspecific language impairmentsuccesstransmission process
中文摘要
项目摘要/摘要
在美国,高达7%的人患有特殊语言障碍(SLI)。SLI影响社区-
能力、学习和社交能力,在学校需要额外的关注。SLI的原因尚不清楚。
然而,双胞胎研究和家庭研究清楚地表明,
这种混乱的传播。已经有几个关于SLI小家庭的连锁研究,但
日期这些研究在确定这种疾病的致病基因方面取得了有限的成功。很少有尝试
在具有独立复制的家系中报告SLI基因座。有必要进一步关注
以家庭为基础的方法,特别是使用近亲家庭来检测SLI基因座,这可以让我们
找出致病基因。这项拟议研究的长期目标是确定与
SLI通过研究从巴基斯坦确定的血亲家庭。最近,一种类似的方法也被使用,
它确定了第一个导致口吃的基因,另一种表型和遗传复杂的疾病-
德尔。我们最初对巴基斯坦14个有血缘关系的SLI家系进行了基因分析。我们的预赛
SLI家系中的连锁图谱提示SLI基因座,这是原理的证明,但它也证明了
需要在来自巴基斯坦的其他SLI家庭中扩大基因图谱和表型。我们提出三个建议
要实现的具体目标。适当年龄的平均数和标准差将以巴基斯坦萨姆计算-
用于多种语言评估的PLES(目标1)。全基因组的基因图谱将被很好地进行-
具有多代血缘关系的SLI家族的特征(目标2)。常见纯合子的频率
将在巴基斯坦样本中估计区域(目标3)。
英文摘要
Project Summary/Abstract
Specific language impairment (SLI) affects up to 7% of individuals in the United States. SLI affects communica-
tion, learning, and social abilities, and requires additional attention in school. The causes of SLI are not known.
However, twin studies and family studies clearly demonstrate that there are genetic components involved in
the transmission of this disorder. There have been several linkage studies of small, outbred SLI families, but to
date these studies have had limited success identifying causative genes for this disorder. Very few attempts
were made to report SLI loci in extended families with independent replication. There is a need for further focus
on a family-based approach, specifically using consanguineous families, to detect SLI loci that can allow us to
identify causative genes. The long-term objectives of the proposed study are to identify genes responsible for
SLI by studying consanguineous families ascertained from Pakistan. Recently, a similar approach was used,
which identified the first gene responsible for stuttering, another phenotypically and genetically complex disor-
der. We initially performed genetic analysis in 14 consanguineous SLI families in Pakistan. Our preliminary
linkage mapping in SLI families suggested SLI loci, which is a proof of principle, but it also demonstrated the
need to extend gene-mapping and phenotyping in additional SLI families from Pakistan. We propose three
specific aims to achieve. Age appropriate means and standard deviations will be calculated in Pakistani sam-
ples for multiple language assessments (Aim#1). Genome-wide gene mapping will be performed in well char-
acterized multigenerational consanguineous SLI families (Aim#2). The frequency of common homozygosity
regions will be estimated in Pakistani samples (Aim#3).
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