Hendricks W M, Ahmad M, Gratz E
Br J Dermatol. 1978 Feb;98(2):175-86. doi: 10.1111/j.1365-2133.1978.tb01619.x.
A review of Weber-Christian syndrome in infancy is presented along with the report of two cases. Both infants had low serum properdin levels, and one patient showed remissions of his disease when he was T-lymphocytopenic. This suggests that the T-lymphocyte may have an important role in the pathogenesis of Weber--Christian syndrome.
本文对婴儿期韦格纳-克里斯蒂安综合征进行了综述，并报告了两例病例。两名婴儿的血清备解素水平均较低，其中一名患者在T淋巴细胞减少时病情缓解。这表明T淋巴细胞可能在韦格纳-克里斯蒂安综合征的发病机制中起重要作用。
