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首页> 外文期刊>The Cleft Palate-Craniofacial Journal >Nonsyndromic Cleft Lip With or Without Cleft Palate in China: Assessment of Candidate Regions
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Nonsyndromic Cleft Lip With or Without Cleft Palate in China: Assessment of Candidate Regions

机译:中国有或没有C裂的非综合征性唇裂:候选区域的评估

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摘要

Objective: Although Asians have the highest birth prevalence of oral-facial clefts, the majority of gene mapping studies of cleft lip with or without cleft palate (CL/P) have been in European or American Caucasians. Therefore, the objective of this study of Chinese families was to evaluate linkage and association between CL/P and 10 genetic markers in five chromosomal regions that have shown positive results in Caucasians.nnSetting: Families were ascertained through nonsyndromic CL/P surgical probands from hospitals throughout Shanghai, China.nnParticipants: Study participants included 671 individuals from 60 families with two or more members affected with oral-facial clefts. Of the 671 total individuals, 145 were affected.nnResults: Ten markers from chromosomes 2, 4, 6, 17, and 19 were assessed (TGFA, MSX1, D4S194, D4S175, F13A1, GATA185H, D17S250, D17S579, D19S49, APOC2). LOD scores were calculated between each of the 10 markers and CL/P as well as model-free statistics of linkage (SimIBD) and association (TDT). None of the markers showed significantly positive LOD scores with CL/P. A significantly positive result (p = .01) was seen using SimIBD for APOC2 on chromosome 19, and a positive TDT result (p = .004) was obtained for D19S49, near APOC2.nnConclusions: This is the first gene mapping study of CL/P in China. These results indicate that most of the genetic regions with positive results in Caucasian families may not be involved in CL/P found in China, although there is some positive evidence for the candidate region on chromosome 19.
机译:目的:尽管亚洲人的口腔裂隙出生率最高,但大多数有或没有裂pa(CL / P)的唇裂基因图谱研究都在欧洲或美国的白种人中进行。因此,本研究的中国家庭的目的是评估在白种人中显示出阳性结果的五个染色体区域中CL / P与10个遗传标记之间的联系和关联.nnSetting:通过医院的非综合征性CL / P手术先证者确定家庭参与者:研究参与者包括来自60个家庭的671个个体,其中两个或更多成员患有口腔裂隙。结果在671个个体中,有145个受到感染.nn结果:评估了10条来自2、4、6、17和19号染色体的标记(TGFA,MSX1,D4S194,D4S175,F13A1,GATA185H,D17S250,D17S579,D19S49,APOC2)。在10个标记和CL / P的每一个之间计算LOD得分,并计算无模型的连锁统计(SimIBD)和关联(TDT)。没有标记显示CL / P的LOD得分显着阳性。使用SimIBD对19号染色体上的APOC2观察到显着阳性结果(p = .01),对APOC2附近的D19S49获得了阳性TDT结果(p = .004)。nn结论:这是CL的第一个基因定位研究/ P在中国。这些结果表明,尽管在第19号染色体上的候选区域有一些肯定的证据,但在中国发现的大多数在白种人家庭中具有阳性结果的遗传区域可能不参与CL / P。

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