A Chinese girl of Blau syndrome with renal arteritis and a literature review

BACKGROUND: Blau syndrome is a rare autoinflammatory disease caused by autosomal dominant mutations in the CARD15/NOD2 gene. Vascular involvement is a rare phenotype in Blau syndrome patients. In this study, we aimed to describe a 20-year- old Chinese girl with Blau syndrome complicated by renal art...

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Detalles Bibliográficos
Autores principales: Zeng, Qiaoqian, Liu, Haimei, Li, Guomin, Li, Yifan, Guan, Wanzhen, Zhang, Tao, Gong, Yinv, Zhang, Xiaomei, Lv, Qianying, Wu, Bingbing, Xu, Hong, Sun, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010039/
https://www.ncbi.nlm.nih.gov/pubmed/36915122
http://dx.doi.org/10.1186/s12969-023-00804-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010039/
https://www.ncbi.nlm.nih.gov/pubmed/36915122
http://dx.doi.org/10.1186/s12969-023-00804-z

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