首页> 外文期刊>Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology >Antenatal detection of cleft lip with or without cleft palate: incidence of associated chromosomal and structural anomalies.
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Antenatal detection of cleft lip with or without cleft palate: incidence of associated chromosomal and structural anomalies.

机译:产前检查有无without裂的唇裂:相关的染色体和结构异常的发生率。

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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.
机译:目的:确定有多少胎儿在出生前被诊断为with裂或无without裂,并伴有先天性结构和/或染色体异常,以及是否与裂或or裂的解剖学类型有关。方法:这是对2000年1月至2006年1月间转诊至英格兰西北部唇Lip裂(CLAP)小组的婴儿的回顾性研究。对同期转诊至地区胎儿管理部门(FMU)的情况进行了调查。以确定相应的产前超声检查结果以及有关终止妊娠和子宫内胎儿死亡的数据。结果:在为期6年的调查中,有570名婴儿被转介到FMU和/或CLAP小组。其中,有24例终止妊娠,确定了2例宫内胎儿死亡和1例早期新生儿死亡。 543例幸存患者中有69例的数据不完整。在188例单侧患者和34例双侧唇left裂患者中,没有其他任何结构异常的核型异常。相关结构异常的发生率随of裂的解剖类型而异:单侧c唇+/- was为9.8%(19/194),双侧left唇和25为25%(11/44),而中线唇left裂为100%(11/11)。 252例孤立的isolated裂病例在产前均未发现。其中5.6%(n = 14)有核型或相关的结构异常,21.0%(n = 53)有遗传综合症作为基础诊断。结论:考虑到left裂的解剖类型以及是否存在相关异常,必须根据具体的扫描诊断来调整患者的产前咨询。为所有患者提供侵入性测试是不合适的。这些患者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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