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伴有遗传易感性的骨髓增生异常综合征

Myelodysplastic syndrome with genetic predisposition.

作者信息

Park Meerim

机构信息

Department of Pediatrics, Center for Pediatric Cancer, National Cancer Center, Goyang, Korea.

出版信息

Blood Res. 2021 Apr 30;56(S1):S34-S38. doi: 10.5045/br.2021.2020327.

Abstract

Myelodysplastic syndrome (MDS) refers to a heterogeneous group of clonal blood disorders characterized by ineffective hematopoiesis, cytopenia, dysplasia, and an increased risk of acute myeloid leukemia (AML). A growing number of inherited genetic loci that contribute to MDS/AML development are rapidly being identified. As genetic sequencing has become increasingly integrated into clinical practice, clearly defined syndromes have emerged, known as the MDS/AML predisposition syndrome. With more patients and families being identified with predisposing conditions, knowledge of the approach of evaluating and managing MDS with genetic predisposition is increasingly essential. This article reviews MDS with genetic predisposition and the practical aspects of management in patients with predisposition syndrome.

摘要

骨髓增生异常综合征(MDS)是一组异质性的克隆性血液疾病,其特征为造血无效、血细胞减少、发育异常以及急性髓系白血病(AML)风险增加。越来越多导致MDS/AML发生的遗传性基因位点正迅速被识别出来。随着基因测序日益融入临床实践,已出现了明确界定的综合征,即MDS/AML易感性综合征。随着越来越多的患者和家庭被发现存在易感状况,了解评估和管理具有遗传易感性的MDS的方法变得越来越重要。本文综述了具有遗传易感性的MDS以及易感性综合征患者管理的实际方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a71/8093994/bbfae8a0bb7e/br-56-s1-34-f1.jpg

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