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Malformations associated with cleft lip and palate in human embryos and fetuses.
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Cleft lip+/-cleft palate: an overview of the literature and an analysis of Danish cases born between 1941 and 1968.唇裂伴或不伴腭裂:文献综述及对1941年至1968年间丹麦出生病例的分析
Am J Med Genet. 1980;6(1):83-97. doi: 10.1002/ajmg.1320060108.
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Cleft palate: a genetic and epidemiologic investigation.腭裂:一项遗传学与流行病学调查。
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7
Genetic analysis of cleft lip with or without cleft palate in Danish kindreds.丹麦家族中唇裂伴或不伴腭裂的基因分析。
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9
A genetic study of cleft lip and palate in Hawaii. II. Complex segregation analysis and genetic risks.夏威夷唇腭裂的遗传学研究。II. 复杂分离分析与遗传风险。
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Sex ratio and cleft lip with or without cleft palate.
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唇腭裂遗传流行病学研究中的选择偏倚。

Selection bias in genetic-epidemiological studies of cleft lip and palate.

作者信息

Christensen K, Holm N V, Olsen J, Kock K, Fogh-Andersen P

机构信息

Institute of Community Health, University Clinic, Odense University, Denmark.

出版信息

Am J Hum Genet. 1992 Sep;51(3):654-9.

PMID:1496993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1682715/
Abstract

The possible impact of selection bias in genetic and epidemiological studies of cleft lip and palate was studied, using three nationwide ascertainment sources and an autopsy study in a 10% sample of the Danish population. A total of 670 cases were identified. Two national record systems, when used together, were found suitable for ascertaining facial cleft in live births. More than 95% ascertainment was obtained by means of surgical files for cleft lip (with or without cleft palate) without associated malformations/syndromes. However, surgical files could be a poor source for studying isolated cleft palate (CP) (only a 60% and biased ascertainment), and they cannot be used to study the prevalence of associated malformations or syndromes in facial cleft cases. The male:female ratio was 0.88 in surgically treated cases of CP and was 1.5 in nonoperated CP cases, making the overall sex ratio for CP 1.1 (95% confidence limits 0.86-1.4) The sex ratio for CP without associated malformation was 1.1 (95% confidence limits 0.84-1.6). One of the major test criteria in CP multifactorial threshold models (higher CP liability among male CP relatives) must be reconsidered, if other investigations confirm that a CP sex-ratio reversal to male predominance occurs when high ascertainment is achieved.

摘要

利用丹麦全国范围内的三个确诊来源以及对10%的丹麦人口样本进行的尸检研究,探讨了唇腭裂基因和流行病学研究中选择偏倚可能产生的影响。共识别出670例病例。发现将两个国家记录系统结合使用,适用于确定活产儿中的面部裂隙。通过手术档案可获得超过95%的唇裂(伴或不伴腭裂)且无相关畸形/综合征病例的确诊信息。然而,手术档案可能不是研究孤立性腭裂(CP)的良好来源(确诊率仅为60%且存在偏倚),并且不能用于研究面部裂隙病例中相关畸形或综合征的患病率。接受手术治疗的CP病例中,男女比例为0.88,未接受手术的CP病例中男女比例为1.5,CP的总体性别比为1.1(95%置信区间为0.86 - 1.4)。无相关畸形的CP性别比为1.1(95%置信区间为0.84 - 1.6)。如果其他调查证实,在高确诊率情况下CP的性别比会反转至男性占主导,那么CP多因素阈值模型中的一个主要测试标准(男性CP亲属中CP易感性更高)必须重新考虑。