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胎儿超声检查发现整倍体胎儿颈部透明带增厚的产前诊断(II):RAS病相关疾病——产前超声检查结果及基因型-表型相关性

Prenatal Diagnosis of Euploid Increased Nuchal Translucency on Fetal Ultrasound (II): RASopathy Disorders - Prenatal Ultrasound Findings and Genotype-phenotype Correlations.

作者信息

Chen Chih-Ping

机构信息

Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan.

Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.

出版信息

J Med Ultrasound. 2022 Nov 9;31(1):13-16. doi: 10.4103/jmu.jmu_79_22. eCollection 2023 Jan-Mar.

Abstract

Prenatal diagnosis of euploid increased nuchal translucency (NT) remains a challenge to obstetricians and genetic counselors, although increased euploid NT at prenatal diagnosis can be associated with a favorable outcome. Prenatal diagnosis of euploid increased NT should include a differential diagnosis of pathogenetic copy number variants and RASopathy disorders (RDs) including Noonan syndrome. Therefore, chromosomal microarray analysis, whole-exome sequencing, RASopathy-disorder testing, and protein-tyrosine phosphatase nonreceptor type 11 gene testing may be necessary under such a circumstance. In this report, a comprehensive review of RDs with its prenatal ultrasound findings and genotype-phenotype correlations is presented.

摘要

整倍体胎儿颈项透明层(NT)增厚的产前诊断对产科医生和遗传咨询师来说仍是一项挑战,尽管产前诊断时整倍体胎儿NT增厚可能与良好的预后相关。整倍体胎儿NT增厚的产前诊断应包括对致病性拷贝数变异和RAS病(RDs)(包括努南综合征)进行鉴别诊断。因此,在这种情况下,可能需要进行染色体微阵列分析、全外显子组测序、RAS病检测和蛋白酪氨酸磷酸酶非受体11型基因检测。在本报告中,我们对RDs及其产前超声检查结果和基因型-表型相关性进行了全面综述。

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本文引用的文献

1
The RASopathies: from pathogenetics to therapeutics.RAS 相关疾病:从发病机制到治疗学。
Dis Model Mech. 2022 Feb 1;15(2). doi: 10.1242/dmm.049107. Epub 2022 Feb 18.
3
Defining RASopathy.定义 RAS opathy。
Dis Model Mech. 2022 Feb 1;15(2). doi: 10.1242/dmm.049344.
5
RASopathies: A significant cause of polyhydramnios?RAS 病:羊水过多的重要病因?
Prenat Diagn. 2021 Feb;41(3):362-367. doi: 10.1002/pd.5862. Epub 2020 Nov 18.
10
Cardiovascular disease in Noonan syndrome.努南综合征相关心血管疾病
Curr Opin Pediatr. 2018 Oct;30(5):601-608. doi: 10.1097/MOP.0000000000000669.

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