摘要

Kawasaki disease (KD) is a leading cause of acquired heart disease in children; however, the etiology of this disease is still unclear. Several genome-wide association studies (GWASs) indicated that genetic variations contribute to KD susceptibility and intravenous immunoglobulin (IVIG) responses. Application genetic risk score is another example of pharmacogenomics research for predicting IVIG unresponsiveness. High-throughput DNA sequencing technology has been developed on an unprecedented scale, and more and more genomic information will be available to understand the etiology and treatment of KD.
原文英語
主出版物標題Kawasaki Disease
發行者Springer Nature
頁面103-116
頁數14
ISBN(電子)9789811929441
ISBN(列印)9789811929434
DOIs
出版狀態已發佈 - 1月 1 2022

ASJC Scopus subject areas

  • 一般醫學

指紋

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