• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.4103/jmu.jmu_79_22
PMID:37180632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10173828/
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。

相似文献

1
Prenatal Diagnosis of Euploid Increased Nuchal Translucency on Fetal Ultrasound (II): RASopathy Disorders - Prenatal Ultrasound Findings and Genotype-phenotype Correlations.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
J Med Ultrasound. 2022 Nov 9;31(1):13-16. doi: 10.4103/jmu.jmu_79_22. eCollection 2023 Jan-Mar.
2
Prenatal Diagnosis of Euploid Increased Nuchal Translucency on Fetal Ultrasound (I): Noonan Syndrome: Prenatal Diagnosis and Genetic Testing.胎儿超声检查发现整倍体性颈部透明带增厚的产前诊断(I):努南综合征:产前诊断与基因检测
J Med Ultrasound. 2022 Nov 9;30(4):257-260. doi: 10.4103/jmu.jmu_78_22. eCollection 2022 Oct-Dec.
3
Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucency.超声检查胎儿颈项透明层增厚与微阵列芯片和 RAS 相关疾病检测。
Ultrasound Obstet Gynecol. 2020 Mar;55(3):383-390. doi: 10.1002/uog.20352.
4
Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era.在 424 例胎儿队列中 rasopathy 的产前超声表现:NGS 时代基因检测的更新。
J Med Genet. 2019 Oct;56(10):654-661. doi: 10.1136/jmedgenet-2018-105746. Epub 2019 Apr 30.
5
The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants.严重的与癌症相关的 PTPN11 变异导致努南综合征的胎儿表型。
Am J Case Rep. 2020 Jul 31;21:e922468. doi: 10.12659/AJCR.922468.
6
Prenatal screening for fetal aneuploidy in singleton pregnancies.单胎妊娠胎儿非整倍体的产前筛查。
J Obstet Gynaecol Can. 2011 Jul;33(7):736-750. doi: 10.1016/S1701-2163(16)34961-1.
7
The 16-week sonographic findings in fetuses with increased nuchal translucency and a normal array.颈部透明带增厚且超声检查正常的胎儿在孕16周时的超声检查结果。
J Matern Fetal Neonatal Med. 2022 Dec;35(25):9435-9439. doi: 10.1080/14767058.2022.2040477. Epub 2022 Feb 20.
8
Antenatal diagnosis of cardio-facio-cutaneous syndrome: Prenatal characteristics and contribution of fetal facial dysmorphic signs in utero. About a case and review of literature.心面皮肤综合征的产前诊断:胎儿面部畸形特征及宫内表现。附一例报告及文献复习。
Eur J Obstet Gynecol Reprod Biol. 2019 Sep;240:232-241. doi: 10.1016/j.ejogrb.2019.06.035. Epub 2019 Jul 16.
9
A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma-Systematic Review of the Literature, Meta-Analysis and Case Series.棘手难题:从对检测到有颈部积液、颈部透明带增厚或囊状水瘤的胎儿进行基因检测中吸取的教训——文献系统综述、荟萃分析及病例系列研究
Diagnostics (Basel). 2022 Dec 23;13(1):48. doi: 10.3390/diagnostics13010048.
10
Whole exome sequencing in fetuses with isolated increased nuchal translucency: a systematic review and meta-analysis.胎儿单纯性颈项透明层增厚的全外显子组测序:系统评价和荟萃分析。
J Matern Fetal Neonatal Med. 2023 Dec;36(1):2193285. doi: 10.1080/14767058.2023.2193285.

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.
2
Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta-analysis.外显子组测序在产前诊断胎儿结构畸形中的诊断效能:系统评价和荟萃分析。
Prenat Diagn. 2022 May;42(6):662-685. doi: 10.1002/pd.6115. Epub 2022 May 7.
3
Defining RASopathy.定义 RAS opathy。
Dis Model Mech. 2022 Feb 1;15(2). doi: 10.1242/dmm.049344.
4
When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort.何时对胎儿进行 RASopathy 检测?基于 352 例多中心病例和一个新生儿队列的系统分析提出的建议。
Genet Med. 2021 Jun;23(6):1116-1124. doi: 10.1038/s41436-020-01093-7. Epub 2021 Feb 10.
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.
6
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.外显子组测序在非免疫性胎儿水肿产前诊断中的应用。
N Engl J Med. 2020 Oct 29;383(18):1746-1756. doi: 10.1056/NEJMoa2023643. Epub 2020 Oct 7.
7
Cardiac manifestations and gene mutations of patients with RASopathies in Taiwan.台湾地区 RAS opathy 患者的心脏表现和基因突变。
Am J Med Genet A. 2020 Feb;182(2):357-364. doi: 10.1002/ajmg.a.61429. Epub 2019 Dec 14.
8
Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucency.超声检查胎儿颈项透明层增厚与微阵列芯片和 RAS 相关疾病检测。
Ultrasound Obstet Gynecol. 2020 Mar;55(3):383-390. doi: 10.1002/uog.20352.
9
Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era.在 424 例胎儿队列中 rasopathy 的产前超声表现:NGS 时代基因检测的更新。
J Med Genet. 2019 Oct;56(10):654-661. doi: 10.1136/jmedgenet-2018-105746. Epub 2019 Apr 30.
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.