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胎儿胼胝体异常:潜在遗传疾病及产前检测选择综述

Fetal Corpus Callosum Anomalies: A Review of Underlying Genetic Disorders and Prenatal Testing Options.

作者信息

Lanzarone Valeria, Eixarch Elisenda, Borrell Antoni

机构信息

Christopher Kohlenberg Department of Perinatal Ultrasound, Nepean Hospital, Sydney, New South Wales, Australia.

BCNatal Fetal Medicine Research Center (Hospital Clınic and Hospital Sant Joan de Deu), University of Barcelona, Barcelona, Catalonia, Spain.

出版信息

J Ultrasound Med. 2025 Apr;44(4):637-652. doi: 10.1002/jum.16639. Epub 2025 Jan 20.

Abstract

Anomalies of the corpus callosum (CC) are amongst the most common fetal Central Nervous System (CNS) anomalies detectable on ultrasound. Underlying genetic disease plays an important part in defining prognosis. Associations with aneuploidy and submicroscopic chromosomal deletions or duplications have been well demonstrated using chromosomal microarray analysis. Next-generation sequencing techniques such as exome sequencing, have revolutionized the ability to detect monogenic disease in these fetuses. In the context of important recent publications on exome sequencing in prenatal populations, an updated review of genetic testing options in CC anomalies is presented.

摘要

胼胝体(CC)异常是超声检查中最常见的胎儿中枢神经系统(CNS)异常之一。潜在的遗传疾病在确定预后方面起着重要作用。使用染色体微阵列分析已充分证明了与非整倍体以及亚微观染色体缺失或重复的关联。外显子组测序等新一代测序技术彻底改变了在这些胎儿中检测单基因疾病的能力。鉴于近期有关产前人群外显子组测序的重要出版物,本文对CC异常的基因检测选项进行了更新综述。

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