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

被引:10
|
作者
Skibenes, Sofie T. [1 ]
Clausen, Ida [1 ]
Raaschou-Jensen, Klas [1 ]
机构
[1] Odense Univ Hosp, Dept Hematol, Odense, Denmark
关键词
Aplastic anaemia; hypoplastic bone marrow failure; hypoplastic myelodysplastic syndrome; inherited bone marrow failure syndromes; next‐ generation sequencing; paroxysmal nocturnal haemoglobinuria; DIAMOND-BLACKFAN ANEMIA; CLONAL HEMATOPOIESIS; MYELODYSPLASTIC SYNDROMES; APLASTIC-ANEMIA; FANCONI-ANEMIA; SOMATIC MUTATIONS; ANDROGEN THERAPY; TET2; MUTATIONS; DIAGNOSIS; AZACITIDINE;
D O I
10.1111/ejh.13513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:3 / 13
页数:11
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