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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
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 |
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