首页> 外文期刊>American journal of medical genetics, Part A >The prevalence of amnion rupture sequence, limb body wall defects and body wall defects in Alberta 1980-2012 with a review of risk factors and familial cases
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The prevalence of amnion rupture sequence, limb body wall defects and body wall defects in Alberta 1980-2012 with a review of risk factors and familial cases

机译:Alberta 1980-2012中Amnion破裂序列,肢体体壁缺陷和身体壁缺陷的患病率,并审查了风险因素和家族性案例

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Prevalence rates of amnion rupture sequence, limb body wall defect, and body wall defects vary widely. Comparisons are difficult due to small case numbers and the lack of agreement of definition, classification, and pathogenesis. This study reports the prevalence of cases classified in five distinct categories. The Alberta Congenital Anomalies Surveillance System data on live births, stillbirths, and terminations of pregnancy (<20 weeks gestation) occurring between 1980 through 2012 with the ICD-10 Royal College of Paediatrics and Child Health Adaptation codes used for congenital constriction bands (Q79.80) and body wall complex (Q89.7) were reviewed. During the 33-year-study period, there were 153 eligible cases ascertained from 1,411,652 live births and stillbirths, giving a prevalence of 1.08/10,000 total births. There were more males (52%) than females (45%) and 3% were of unknown sex. The average maternal age, birth weight, and gestation was 27 years, 2,701g, and 35 weeks, respectively. Limb deficiencies occurred in 78% of cases. Amniotic bands with limb deficiency was the most common phenotype (48%). Digital limb deficiency was the most frequent type (56%); however, cases with body wall defects had more severe types of limb deficiencies. The upper limbs only were affected more times (44%), and there was no side preference. Most cases are sporadic but a number of familial occurrences have been reported although some have insufficient documentation and others misdiagnosed. A review of putative risk factors gives conflicting results. (c) 2016 Wiley Periodicals, Inc.
机译:羊膜破裂序列,肢体体壁缺陷和体壁缺陷的流行率随着广泛的差异而变化。由于小案例数量和缺乏定义,分类和发病机制,比较难以困难。本研究报告了五个不同类别分类的案件的患病率。艾伯塔省先天性异常监测系统存在于1980年至2012年之间的活产出生物,死产和终止(<20周的妊娠)与先天性收缩频段的ICD-10皇家儿童健康适应码发生在1980年至2012年间80)和身体墙复合体(Q89.7)进行了审查。在33岁的研究期间,有153例符合条件的案件,可从1,411,652个活产前进行,患有1.08 / 10,000个出生的患病率。比女性更多的男性(52%)(45%),3%的性别也是未知的性别。平均母体年龄,出生体重和妊娠分别为27岁,2,701克和35周。 78%的病例发生了肢体缺陷。患有肢体缺乏的羊膜是最常见的表型(48%)。数字肢体缺乏是最常见的类型(56%);然而,具有身体墙壁缺陷的病例具有更严重的肢体缺陷。上肢仅受影响更多的次数(44%),没有侧面偏好。大多数病例是零星的,但虽然有些人没有足够的文档和其他误会,但已经报告了许多家庭出现。调整危险因素审查给出了相互矛盾的结果。 (c)2016 Wiley期刊,Inc。

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