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产前检测唇裂伴或不伴腭裂:相关染色体和结构异常的发生率。

Antenatal detection of cleft lip with or without cleft palate: incidence of associated chromosomal and structural anomalies.

机构信息

Fetal Management Unit, St Marys Hospital, Manchester, UK.

出版信息

Ultrasound Obstet Gynecol. 2009 Oct;34(4):410-5. doi: 10.1002/uog.6447.

Abstract

OBJECTIVE

To ascertain how many fetuses with prenatally diagnosed cleft lip with or without cleft palate have associated congenital structural and/or chromosomal abnormalities and whether there is an association with the anatomical type of cleft lip or palate.

METHODS

This was a retrospective review of infants referred to the North-West England Regional Cleft Lip and Palate (CLAP) team between January 2000 and January 2006. Referrals made to the Regional Fetal Management Unit (FMU) in the same time period were investigated to identify the corresponding antenatal ultrasound findings and data on termination of pregnancy and intrauterine fetal death.

RESULTS

Over the 6-year period investigated, 570 infants were referred to the FMU and/or CLAP team. Among these, there were 24 terminations of pregnancy, two intrauterine fetal deaths and one early neonatal death identified. Data on 69 of the 543 patients that survived were incomplete. Of 188 cases with unilateral and 34 cases with bilateral cleft lip +/- palate there were no karyotypical abnormalities without other structural abnormalities. The incidence of associated structural abnormalities varied with the anatomical type of cleft: that of unilateral cleft lip +/- palate was 9.8% (19/194), that of bilateral cleft lip and palate was 25% (11/44) and that of midline cleft lip and palate was 100% (11/11). None of 252 cases with isolated cleft palate was identified antenatally; of these, 5.6% (n = 14) had either karyotypical or associated structural abnormalities and 21.0% (n = 53) had a genetic syndrome as an underlying diagnosis.

CONCLUSIONS

It is essential to tailor the antenatal counseling of patients to the specific scan diagnosis, considering both the anatomical type of cleft and the presence or absence of associated abnormalities. It is inappropriate to offer invasive testing to all patients. The use of three-dimensional ultrasound as an adjunct should be considered in these patients to improve the accuracy of prenatal diagnosis.

摘要

目的

确定有多少产前诊断为唇裂伴或不伴腭裂的胎儿伴有先天性结构和/或染色体异常,以及唇裂或腭裂的解剖类型是否与之相关。

方法

这是对 2000 年 1 月至 2006 年 1 月期间向英格兰西北部地区唇腭裂(CLAP)团队转诊的婴儿进行的回顾性研究。对同期转至区域胎儿管理单位(FMU)的病例进行调查,以确定相应的产前超声发现以及终止妊娠和宫内胎儿死亡的数据。

结果

在所研究的 6 年期间,有 570 名婴儿被转至 FMU 和/或 CLAP 团队。其中,有 24 例终止妊娠,2 例宫内胎儿死亡,1 例新生儿早期死亡。69 例存活患儿的 543 例数据不完整。在 188 例单侧和 34 例双侧唇裂伴或不伴腭裂的病例中,没有核型异常而无其他结构异常的病例。伴发结构异常的发生率随裂的解剖类型而变化:单侧唇裂伴或不伴腭裂为 9.8%(19/194),双侧唇腭裂为 25%(11/44),中线唇腭裂为 100%(11/11)。未在 252 例单纯腭裂的病例中发现产前异常;其中,5.6%(n=14)有核型或伴发结构异常,21.0%(n=53)有潜在诊断为遗传综合征。

结论

对患者进行产前咨询时,务必根据具体的扫描诊断,同时考虑裂的解剖类型和是否存在伴发异常。对所有患者进行有创性检查是不适当的。在这些患者中,应考虑使用三维超声作为辅助手段,以提高产前诊断的准确性。

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