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遗传性血小板疾病的基因分类与确诊:韩国的现状

Genetic classification and confirmation of inherited platelet disorders: current status in Korea.

作者信息

Shim Ye Jee

机构信息

Department of Pediatrics, Keimyung University School of Medicine, Keimyung University Dongsan Medical Center, Daegu, Korea.

出版信息

Clin Exp Pediatr. 2020 Mar;63(3):79-87. doi: 10.3345/kjp.2019.00052. Epub 2020 Feb 6.

Abstract

Inherited platelet disorders (IPDs), which manifest as primary hemostasis defects, often underlie abnormal bleeding and a family history of thrombocytopenia, bone marrow failure, hematologic malignancies, undefined mucocutaneous bleeding disorder, or congenital bony defects. Wide heterogeneity in IPD types with regard to the presence or absence of thrombocytopenia, platelet dysfunction, bone marrow failure, and dysmegakaryopoiesis is observed in patients. The individual processes involved in platelet production and hemostasis are genetically controlled; to date, mutations of more than 50 genes involved in various platelet biogenesis steps have been implicated in IPDs. Representative IPDs resulting from defects in specific pathways, such as thrombopoietin/MPL signaling; transcriptional regulation; granule formation, trafficking, and secretion; proplatelet formation; cytoskeleton regulation; and transmembrane glycoprotein signaling are reviewed, and the underlying gene mutations are discussed based on the National Center for Biotechnology Information database and Online Mendelian Inheritance in Man accession number. Further, the status and prevalence of genetically confirmed IPDs in Korea are explored based on searches of the PubMed and KoreaMed databases. IPDs are congenital bleeding disorders that can be dangerous due to unexpected bleeding and require genetic counseling for family members and descendants. Therefore, the pediatrician should be suspicious and aware of IPDs and perform the appropriate tests if the patient has unexpected bleeding. However, all IPDs are extremely rare; thus, the domestic incidences of IPDs are unclear and their diagnosis is difficult. Diagnostic confirmation or differential diagnoses of IPDs are challenging, time-consuming, and expensive, and patients are frequently misdiagnosed. Comprehensive molecular characterization and classification of these disorders should enable accurate and precise diagnosis and facilitate improved patient management.

摘要

遗传性血小板疾病(IPDs)表现为原发性止血缺陷,常是异常出血以及血小板减少、骨髓衰竭、血液系统恶性肿瘤、不明原因的黏膜皮肤出血性疾病或先天性骨缺陷家族史的基础。在患者中观察到IPD类型在血小板减少、血小板功能障碍、骨髓衰竭和巨核细胞生成异常的有无方面存在广泛的异质性。血小板生成和止血过程中的各个环节都受基因控制;迄今为止,参与各种血小板生物发生步骤的50多个基因的突变与IPDs有关。本文综述了由特定途径缺陷导致的代表性IPDs,如血小板生成素/MPL信号传导、转录调控、颗粒形成、运输和分泌、前血小板形成、细胞骨架调控以及跨膜糖蛋白信号传导,并根据美国国立生物技术信息中心数据库和《人类孟德尔遗传在线》登录号讨论了潜在的基因突变。此外,通过检索PubMed和KoreaMed数据库,探讨了韩国基因确诊的IPDs的现状和患病率。IPDs是先天性出血性疾病,可能因意外出血而危险,需要为家庭成员和后代提供遗传咨询。因此,如果患者出现意外出血,儿科医生应怀疑并了解IPDs,并进行适当的检查。然而,所有IPDs都极为罕见;因此,IPDs在国内的发病率尚不清楚,诊断也很困难。IPDs的诊断确认或鉴别诊断具有挑战性、耗时且昂贵,患者经常被误诊。对这些疾病进行全面的分子特征分析和分类应能实现准确精确的诊断,并有助于改善患者管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2046/7073384/759862740fa6/kjp-2019-00052f1.jpg

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