最先进的靶向高通量测序检测遗传性血小板疾病。

IF 2.7 4区 医学 Q2 HEMATOLOGY
Jennifer Gebetsberger, Kristina Mott, Aline Bernar, Eva Klopocki, Werner Streif, Harald Schulze
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引用次数: 1

摘要

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

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.

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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.
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