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基于大规模人群登记处的唐氏综合征个体异常情况。

Anomalies in Down syndrome individuals in a large population-based registry.

作者信息

Torfs C P, Christianson R E

机构信息

California Birth Defects Monitoring Program, Emeryville 94608, USA.

出版信息

Am J Med Genet. 1998 Jun 5;77(5):431-8.

PMID:9632176
Abstract

In a population of close to 2.5 million infants born from 1983 to 1993 registered in the California Birth Defects Monitoring Program, we compared the prevalence of structural birth defects among 2,894 infants with Down syndrome (DS) with that of infants without DS. Among 61 defects uniformly ascertained in affected and unaffected infants, 45 were significantly more common in DS, with atrioventricular canal (risk ratio = 1,009), duodenal atresia (risk ratio = 265), and annular pancreas (risk ratio = 430) being the most common. Most defects of blastogenesis and most midline defects were either nonsignificantly associated or not observed in infants with DS. Theories on the pathogenesis of defects in trisomies must account for the lack of and for the presence of specific defects.

摘要

在加利福尼亚出生缺陷监测项目中登记的1983年至1993年出生的近250万婴儿群体中,我们比较了2894例唐氏综合征(DS)婴儿与非DS婴儿的结构出生缺陷患病率。在受影响和未受影响婴儿中均能统一确定的61种缺陷中,45种在DS婴儿中明显更为常见,其中房室管(风险比=1009)、十二指肠闭锁(风险比=265)和环状胰腺(风险比=430)最为常见。大多数胚胎发生缺陷和大多数中线缺陷在DS婴儿中要么无显著关联,要么未观察到。关于三体综合征中缺陷发病机制的理论必须解释特定缺陷的缺乏和存在情况。

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