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与主要先天性异常相关的肢体缺陷:来自国际出生缺陷监测系统信息交换所的临床与流行病学研究

Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems.

作者信息

Rosano A, Botto L D, Olney R S, Khoury M J, Ritvanen A, Goujard J, Stoll C, Cocchi G, Merlob P, Mutchinick O, Cornel M C, Castilla E E, Martínez-Frías M L, Zampino G, Erickson J D, Mastroiacovo P

机构信息

International Centre for Birth Defects, Rome, Italy.

出版信息

Am J Med Genet. 2000 Jul 17;93(2):110-6. doi: 10.1002/1096-8628(20000717)93:2<110::aid-ajmg6>3.0.co;2-9.

DOI:10.1002/1096-8628(20000717)93:2<110::aid-ajmg6>3.0.co;2-9
PMID:10869112
Abstract

Although limb defects associated with other congenital anomalies are rarely studied, they may provide insights into limb development that may be useful for etiologic studies and public health monitoring. We pooled data from 11 birth defect registries that are part of the International Clearinghouse for Birth Defects Monitoring Systems. We identified 666 infants, born from 1983 through 1993, who had a non-syndromal limb defect plus at least one other major malformation (rate 12.9/100,000 population). We used observed/expected ratios and log-linear models to detect association patterns. We found that specific limb defects occurred with relatively distinct sets of malformations. Preaxial limb defects occurred more frequently with microtia, esophageal atresia, anorectal atresia, heart defects, unilateral kidney dysgenesis, and some axial skeleton defects; postaxial defects with hypospadias; transverse defects with craniofacial defects, micrognathia, ring constrictions, and muscular defects; intercalary defects with omphalocele; split hand/foot with encephalocele; and amelia with anorectal atresia, omphalocele, severe genitalia defects, unilateral kidney dysgenesis, gastroschisis, and ring constriction. Log-linear modeling identified higher order associations among some of these same malformations.

摘要

虽然与其他先天性异常相关的肢体缺陷很少被研究,但它们可能为肢体发育提供见解,这对病因学研究和公共卫生监测可能有用。我们汇总了来自国际出生缺陷监测系统信息交换所的11个出生缺陷登记处的数据。我们确定了666名在1983年至1993年出生的婴儿,他们患有非综合征性肢体缺陷以及至少一种其他主要畸形(发病率为12.9/100,000人口)。我们使用观察值/期望值比率和对数线性模型来检测关联模式。我们发现特定的肢体缺陷与相对不同的畸形组合相关。轴前肢体缺陷更常伴有小耳畸形、食管闭锁、肛门直肠闭锁、心脏缺陷、单侧肾发育不全以及一些轴向骨骼缺陷;轴后缺陷伴有尿道下裂;横向缺陷伴有颅面缺陷、小颌畸形、环状缩窄和肌肉缺陷;间插性缺陷伴有脐膨出;裂手/裂足伴有脑膨出;以及无肢畸形伴有肛门直肠闭锁、脐膨出、严重生殖器缺陷、单侧肾发育不全、腹裂和环状缩窄。对数线性建模确定了其中一些相同畸形之间的高阶关联。

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