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胎儿颅骨缝早闭的产前超声诊断

Prenatal ultrasound diagnosis of fetal craniosynostosis.

作者信息

Delahaye S, Bernard J P, Rénier D, Ville Y

机构信息

Fetal Medicine Unit, Poissy-St Germain Hospital, France.

出版信息

Ultrasound Obstet Gynecol. 2003 Apr;21(4):347-53. doi: 10.1002/uog.91.

Abstract

OBJECTIVE

Craniosynostosis is defined as the premature closure of the calvarial sutures. The prevalence of this heterogeneous condition is 1 in 2000 and approximately 100 different forms have been described with an established genetic transmission in half of them. Prenatal diagnosis of craniosynostosis relies mainly on identification of associated anomalies and molecular analysis of fetal DNA, which is only feasible in some syndromic forms and in well-documented families. The objective of this study was to investigate the value of prenatal ultrasound examination of cranial sutures in fetuses at risk for craniosynostosis.

METHODS

Forty fetuses at risk for craniosynostosis on the basis of either a family history (Group 1, n = 16) or skull deformity suspected on a first-level fetal ultrasound examination (Group 2, n = 24) were retrospectively investigated. Craniosynostosis was suspected on the basis of skull deformities when present, however the diagnosis was only made in cases where there was a loss of hypoechogenicity of the normal sutures. All infants had both clinical and radiological investigations performed postnatally.

RESULTS

In Group 1, serial ultrasound examination from 12 weeks' gestation onwards led to accurate prenatal diagnosis in all 16 cases. Dysmorphism and skull deformity preceded closure of the sutures by 4 to 16 weeks. In Group 2, prenatal diagnosis was correct in 23/24 cases. There were no false-negative results in either group.

CONCLUSIONS

This series questions further the uncertain genetic determinism of craniosynostosis and seems to rule out the hypothesis of a deformation sequence following primary closure of the cranial sutures. It also suggests that ultrasound examination is useful to demonstrate closure of the sutures in the third trimester of pregnancy in most affected cases.

摘要

目的

颅缝早闭被定义为颅骨缝线的过早闭合。这种异质性疾病的患病率为1/2000,已描述了约100种不同形式,其中一半具有明确的遗传传递方式。颅缝早闭的产前诊断主要依赖于相关异常的识别以及胎儿DNA的分子分析,这仅在某些综合征形式和记录完善的家族中可行。本研究的目的是探讨对有颅缝早闭风险的胎儿进行颅骨缝线产前超声检查的价值。

方法

回顾性研究了40例有颅缝早闭风险的胎儿,其中16例基于家族史(第1组),24例基于一级胎儿超声检查怀疑有颅骨畸形(第2组)。当存在颅骨畸形时怀疑有颅缝早闭,但仅在正常缝线低回声消失的情况下做出诊断。所有婴儿出生后均进行了临床和放射学检查。

结果

在第1组中,从妊娠12周起进行的系列超声检查在所有16例中均做出了准确的产前诊断。畸形和颅骨畸形在缝线闭合前4至16周出现。在第2组中,24例中有23例产前诊断正确。两组均无假阴性结果。

结论

本系列研究进一步质疑了颅缝早闭不确定的遗传决定因素,似乎排除了颅骨缝线原发性闭合后变形序列的假说。它还表明,超声检查有助于在大多数受影响病例的妊娠晚期显示缝线闭合情况。

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