SCHMC

Diagnostic workup of inherited platelet disorders

Metadata Downloads
Abstract
Inherited platelet disorders (IPDs) can cause mucocutaneous bleeding due to impaired primary hemostatic function of platelets, thrombocytopenia, or both. Recent advances in molecular technology can help identify many genes related to platelet biology, control the overall steps of megakaryopoiesis, and cause IPD. In this article, currently available laboratory tools for diagnosing IPDs with the characteristic laboratory features of each IPD are reviewed, and a general diagnostic approach for the evaluation of IPD patients is presented.
All Author(s)
B. Kim
Issued Date
2022
Type
Article
Keyword
Inherited platelet disorderPlatelet function testsThrombocytopeniaBernard-Soulier syndromeMYH9Gray platelet syndromeGlanzmann thrombasthenia
Publisher
대한혈액학회
ISSN
2287-979X ; 2288-0011
Citation Title
Blood Research
Citation Volume
57
Citation Number
S1
Citation Start Page
11
Citation End Page
19
Language(ISO)
eng
DOI
10.5045/br.2022.2021223
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/1570
Appears in Collections:
진단검사의학과 > 1. Journal Papers
공개 및 라이선스
  • 공개 구분공개
파일 목록

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.