基因检测
血小板疾病
生物
遗传学
病因学
遗传变异
血小板紊乱
生物信息学
医学
基因
免疫学
病理
基因型
血小板
血小板聚集
作者
Julia T. Warren,Jorge Di Paola
出处
期刊:Blood
[American Society of Hematology]
日期:2022-02-15
卷期号:139 (22): 3264-3277
被引量:25
标识
DOI:10.1182/blood.2020009300
摘要
The inherited thrombocytopenia syndromes are a group of disorders characterized primarily by quantitative defects in platelet number, though with a variety demonstrating qualitative defects and/or extrahematopoietic findings. Through collaborative international efforts applying next-generation sequencing approaches, the list of genetic syndromes that cause thrombocytopenia has expanded significantly in recent years, now with over 40 genes implicated. In this review, we focus on what is known about the genetic etiology of inherited thrombocytopenia syndromes and how the field has worked to validate new genetic discoveries. We highlight the important role for the clinician in identifying a germline genetic diagnosis and strategies for identifying novel causes through research-based endeavors.
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