Overview of inherited bone marrow failure syndromes

被引:12
|
作者
Park, Meerim [1 ]
机构
[1] Natl Canc Ctr, Ctr Pediat Canc, Dept Pediat, 323 Ilsan Ro, Goyang 10408, South Korea
关键词
Inherited bone marrow failure syndrome; DNA repair; Telomere; Ribosome; Stem cell regulation; TELOMERE LENGTH; CONGENITAL THROMBOCYTOPENIA; MUTATIONS; MECHANISMS; PATTERNS; NEONATE; ANEMIA; CANCER;
D O I
10.5045/br.2022.2022012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with inherited bone marrow failure syndrome (IBMFS) can develop peripheral blood cytopenia, which can ultimately progress to myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). Although some cases of IBMFS are diagnosed based on their typical presentation, variable disease penetrance and expressivity may result in diagnostic dilemmas. With recent advances in genomic evaluation including next-generation sequencing, many suspected cases of IBMFS with atypical presentations can be identified. Identification of the genetic causes of IBMFS has led to important advances in understanding DNA repair, telomere biology, ribosome biogenesis, and hematopoietic stem cell regulation. An overview of this syndromes is summarized in this paper.
引用
收藏
页码:49 / 54
页数:6
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