Case Report: A Novel CXCR4 Mutation in a Chinese Child With Kawasaki Disease Causing WHIM Syndrome

WHIM syndrome, an extremely rare congenital disease with combined immunodeficiency, is mainly caused by heterozygous gain-of-function mutation in the CXCR4 gene. There have been no previous case reports of WHIM syndrome with Kawasaki disease. We herein report a case of a boy who developed Kawasaki d...

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Detalles Bibliográficos
Autores principales: Ma, Xiaopeng, Wang, Yaping, Wu, Peng, Kang, Meiyun, Hong, Yue, Xue, Yao, Chen, Chuqin, Li, Huimin, Fang, Yongjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043559/
https://www.ncbi.nlm.nih.gov/pubmed/35493524
http://dx.doi.org/10.3389/fimmu.2022.857527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043559/
https://www.ncbi.nlm.nih.gov/pubmed/35493524
http://dx.doi.org/10.3389/fimmu.2022.857527

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