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

Author:

Gebetsberger Jennifer1,Mott Kristina2ORCID,Bernar Aline1,Klopocki Eva3,Streif Werner1,Schulze Harald24ORCID

Affiliation:

1. Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Tirol, Austria

2. Institute of Experimental Biomedicine, University Hospital Würzburg, Würzburg, Germany

3. Institute of Human Genetics, University of Würzburg, Würzburg, Germany

4. Center for Rare Blood Cell Disorders, Center for Rare Diseases, University Hospital Würzburg, Würzburg, Germany

Abstract

AbstractInherited 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.

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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