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产前超声检查颅面部异常。

Prenatal ultrasonography of craniofacial abnormalities.

作者信息

Mak Annisa Shui Lam, Leung Kwok Yin

机构信息

Department of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Hong Kong SAR, China.

出版信息

Ultrasonography. 2019 Jan;38(1):13-24. doi: 10.14366/usg.18031. Epub 2018 Jul 3.

Abstract

Craniofacial abnormalities are common. It is important to examine the fetal face and skull Epub ahead of print during prenatal ultrasound examinations because abnormalities of these structures may indicate the presence of other, more subtle anomalies, syndromes, chromosomal abnormalities, or even rarer conditions, such as infections or metabolic disorders. The prenatal diagnosis of craniofacial abnormalities remains difficult, especially in the first trimester. A systematic approach to the fetal skull and face can increase the detection rate. When an abnormality is found, it is important to perform a detailed scan to determine its severity and search for additional abnormalities. The use of 3-/4-dimensional ultrasound may be useful in the assessment of cleft palate and craniosynostosis. Fetal magnetic resonance imaging can facilitate the evaluation of the palate, micrognathia, cranial sutures, brain, and other fetal structures. Invasive prenatal diagnostic techniques are indicated to exclude chromosomal abnormalities. Molecular analysis for some syndromes is feasible if the family history is suggestive.

摘要

颅面异常很常见。在产前超声检查中提前检查胎儿面部和颅骨(电子版提前印刷)很重要,因为这些结构的异常可能表明存在其他更细微的异常、综合征、染色体异常,甚至是更罕见的情况,如感染或代谢紊乱。颅面异常的产前诊断仍然困难,尤其是在孕早期。对胎儿颅骨和面部采用系统的检查方法可以提高检出率。当发现异常时,进行详细扫描以确定其严重程度并寻找其他异常很重要。使用三维/四维超声可能有助于腭裂和颅缝早闭的评估。胎儿磁共振成像有助于腭、小颌畸形、颅缝、脑和其他胎儿结构的评估。需采用侵入性产前诊断技术排除染色体异常。如果家族史提示有某些综合征,进行分子分析是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722f/6323313/e5f37c6a9fb7/usg-18031f1.jpg

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