State-of-the-Art Targeted High-Throughput Sequencing for Detecting Inherited Platelet Disorders.

IF 2.7 4区 医学 Q2 HEMATOLOGY Hamostaseologie Pub Date : 2023-08-01 DOI:10.1055/a-2099-3266
Jennifer Gebetsberger, Kristina Mott, Aline Bernar, Eva Klopocki, Werner Streif, Harald Schulze
{"title":"State-of-the-Art Targeted High-Throughput Sequencing for Detecting Inherited Platelet Disorders.","authors":"Jennifer Gebetsberger,&nbsp;Kristina Mott,&nbsp;Aline Bernar,&nbsp;Eva Klopocki,&nbsp;Werner Streif,&nbsp;Harald Schulze","doi":"10.1055/a-2099-3266","DOIUrl":null,"url":null,"abstract":"<p><p>Inherited platelet disorders (IPDs) are a heterogeneous group of rare entities caused by molecular divergence in genes relevant for platelet formation and function. A rational diagnostic approach is necessary to counsel and treat patients with IPDs. With the introduction of high-throughput sequencing at the beginning of this millennium, a more accurate diagnosis of IPDs has become available. We discuss advantages and limitations of genetic testing, technical issues, and ethical aspects. Additionally, we provide information on the clinical significance of different classes of variants and how they are correctly reported.</p>","PeriodicalId":55074,"journal":{"name":"Hamostaseologie","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hamostaseologie","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1055/a-2099-3266","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Inherited platelet disorders (IPDs) are a heterogeneous group of rare entities caused by molecular divergence in genes relevant for platelet formation and function. A rational diagnostic approach is necessary to counsel and treat patients with IPDs. With the introduction of high-throughput sequencing at the beginning of this millennium, a more accurate diagnosis of IPDs has become available. We discuss advantages and limitations of genetic testing, technical issues, and ethical aspects. Additionally, we provide information on the clinical significance of different classes of variants and how they are correctly reported.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
最先进的靶向高通量测序检测遗传性血小板疾病。
遗传性血小板疾病(IPDs)是一种由血小板形成和功能相关基因的分子分化引起的异质性罕见疾病。合理的诊断方法对ipd患者的咨询和治疗是必要的。随着本世纪初高通量测序的引入,ipd的更准确诊断已经成为可能。我们讨论了基因检测的优点和局限性,技术问题和伦理方面。此外,我们还提供了不同类型变异的临床意义以及如何正确报告的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Hamostaseologie
Hamostaseologie HEMATOLOGY-
CiteScore
5.50
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Hämostaseologie is an interdisciplinary specialist journal on the complex topics of haemorrhages and thromboembolism and is aimed not only at haematologists, but also at a wide range of specialists from clinic and practice. The readership consequently includes both specialists for internal medicine as well as for surgical diseases.
期刊最新文献
Expert Opinion for Defining a Severe Bleeding Phenotype to Guide Prophylaxis in Patients with Nonsevere Hemophilia. Machine-Learning Applications in Thrombosis and Hemostasis. Management of Adult Patients with Newly Diagnosed or Relapsed Primary Immune Thrombocytopenia in Eastern Austria. Treatment of Cancer-Associated Thrombosis: An Update. Primary Prevention of Cancer-Associated Thrombosis: Current Perspectives.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1