Next-generation sequencing in hypoplastic bone marrow failure: What difference does it make?

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Abstract

Hypoplastic bone marrow failure is a diagnostic feature of multiple haematological disorders, which also share a substantial overlap of clinical symptoms. Hence, discrimination of underlying disorders in patients presenting with hypoplastic bone marrow failure remains a major challenge in the clinic. Recent next-generation sequencing (NGS) studies have broadened our understanding of the varying molecular mechanisms and advanced diagnostics of disorders exhibiting hypoplastic bone marrow failure. In this article, we present a literature review of NGS studies of haematological disorders associated with hypoplastic bone marrow failure and highlight the relevance of NGS for improved clinical diagnostics and decision-making.

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Skibenes, S. T., Clausen, I., & Raaschou-Jensen, K. (2021, January 1). Next-generation sequencing in hypoplastic bone marrow failure: What difference does it make? European Journal of Haematology. Blackwell Publishing Ltd. https://doi.org/10.1111/ejh.13513

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