阵发性夜间血红蛋白尿
骨髓衰竭
再生障碍性贫血
医学
骨髓增生异常综合症
骨髓
造血
血红蛋白尿
贫血
癌症的体细胞进化
免疫学
干细胞
内科学
癌症
遗传学
生物
作者
Tetsuichi Yoshizato,Hideki Makishima
出处
期刊:PubMed
日期:2016-01-01
卷期号:57 (12): 2519-2525
被引量:1
标识
DOI:10.11406/rinketsu.57.2519
摘要
Acquired bone marrow failure syndromes consist of aplastic anemia, paroxysmal nocturnal hemoglobinuria (PNH), and myelodysplastic syndromes (MDS). Clonal hematopoiesis is frequently observed in non-neoplastic disorders, aplastic anemia and PNH as well as a neoplastic phenotype, MDS. However, the significance of such clonal hematopoiesis, particularly in aplastic anemia, remains to be elucidated. Recent advancements in next generation sequencing technology have revealed a diverse clonal structure in these bone marrow failure syndromes, as well as in age-related clonal hematopoiesis in healthy people. In this review article, we describe gene mutations in bone marrow failure syndromes, together with those detected in healthy people.
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