VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
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KeAi Communications Co., Ltd.
2025-09-01
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| Series: | Genes and Diseases |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2352304225000297 |
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| _version_ | 1850084917724053504 |
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| author | Yu Tang Hongfei Cui Hongjun Zhao Hui Luo Xiaoxia Zuo Junjiao Wu |
| author_facet | Yu Tang Hongfei Cui Hongjun Zhao Hui Luo Xiaoxia Zuo Junjiao Wu |
| author_sort | Yu Tang |
| collection | DOAJ |
| format | Article |
| id | doaj-art-5016d80dc3f64cac8c5d3d45208b7ab0 |
| institution | DOAJ |
| issn | 2352-3042 |
| language | English |
| publishDate | 2025-09-01 |
| publisher | KeAi Communications Co., Ltd. |
| record_format | Article |
| series | Genes and Diseases |
| spelling | doaj-art-5016d80dc3f64cac8c5d3d45208b7ab02025-08-20T02:43:53ZengKeAi Communications Co., Ltd.Genes and Diseases2352-30422025-09-0112510154010.1016/j.gendis.2025.101540VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosisYu Tang0Hongfei Cui1Hongjun Zhao2Hui Luo3Xiaoxia Zuo4Junjiao Wu5Aging Research Center, Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, ChinaAging Research Center, Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, ChinaNational Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Provincial Clinical Research Center for Rheumatic and Immunologic Diseases, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Hunan Provincial Skin Immunization and Medical Center, Changsha, Hunan 410008, ChinaNational Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Provincial Clinical Research Center for Rheumatic and Immunologic Diseases, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Hunan Provincial Skin Immunization and Medical Center, Changsha, Hunan 410008, ChinaNational Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Provincial Clinical Research Center for Rheumatic and Immunologic Diseases, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Hunan Provincial Skin Immunization and Medical Center, Changsha, Hunan 410008, ChinaCorresponding author. Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Provincial Clinical Research Center for Rheumatic and Immunologic Diseases, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China; Hunan Provincial Skin Immunization and Medical Center, Changsha, Hunan 410008, Chinahttp://www.sciencedirect.com/science/article/pii/S2352304225000297 |
| spellingShingle | Yu Tang Hongfei Cui Hongjun Zhao Hui Luo Xiaoxia Zuo Junjiao Wu VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis Genes and Diseases |
| title | VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis |
| title_full | VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis |
| title_fullStr | VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis |
| title_full_unstemmed | VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis |
| title_short | VEXAS syndrome caused by a UBA1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis |
| title_sort | vexas syndrome caused by a uba1 mutation is complicated by recurrent infections leading to hemophagocytic lymphohistiocytosis |
| url | http://www.sciencedirect.com/science/article/pii/S2352304225000297 |
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