期刊
RHEUMATOLOGY INTERNATIONAL
卷 33, 期 3, 页码 763-766出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00296-010-1645-5
关键词
Hypocomplementemia; Urticarial vasculitis; Child; Familial; Lupus
类别
Hypocomplementemic urticarial vasculitis syndrome (HUVS) is relatively uncommon and generally seen in the fourth decade of life. There are very few pediatric cases with the diagnosis of HUVS in the literature. In this report, we describe the first familial cases of HUVS in three siblings. The disease onset was during childhood period in all patients. One of them developed severe renal involvement and died. The other two had ongoing skin and eye manifestations and the elder one developed lupus. Presence of these three patients is a strong evidence for the role of genetic factors in the pathogenesis of this rare vasculitis.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据