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Research advances in genetic polymorphisms in Kawasaki disease / 中国当代儿科杂志
Article in Zh | WPRIM | ID: wpr-1009874
Responsible library: WPRO
ABSTRACT
Kawasaki disease (KD) is a systemic inflammatory vascular disorder that predominantly affects children and is the leading cause of acquired heart disease in children. Although the etiology of this disease remains unclear, genome-wide association and genome-wide linkage studies have shown that some susceptible genes and chromosomal regions are associated with the development and progression of KD. With the advancement of high-throughput DNA sequencing techniques, more and more genomic information related to KD is being discovered. Understanding the genes involved in the pathogenesis of KD may provide novel insights into the diagnosis and treatment of KD. By analyzing related articles and summarizing related research advances, this article mainly discusses the T cell activation-enhancing genes that have been confirmed to be closely associated with the development and progression of KD and reveals their association with the pathogenesis of KD and coronary artery lesions.
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Full text: 1 Index: WPRIM Main subject: Polymorphism, Genetic / Coronary Vessels / Genetic Predisposition to Disease / Polymorphism, Single Nucleotide / Genome-Wide Association Study / Mucocutaneous Lymph Node Syndrome Limits: Child / Humans Language: Zh Journal: Chinese Journal of Contemporary Pediatrics Year: 2023 Type: Article
Full text: 1 Index: WPRIM Main subject: Polymorphism, Genetic / Coronary Vessels / Genetic Predisposition to Disease / Polymorphism, Single Nucleotide / Genome-Wide Association Study / Mucocutaneous Lymph Node Syndrome Limits: Child / Humans Language: Zh Journal: Chinese Journal of Contemporary Pediatrics Year: 2023 Type: Article