Roord J J, Daha M, Kuis W, Verbrugh H A, Verhoef J, Zegers B J, Stoop J W
Pediatrics. 1983 Jan;71(1):81-7.
A family is described in which 3/11 children showed a homozygous deficiency of C3, and both parents and six other children had subnormal levels of C3. The three children with selective C3 deficiency suffered repeatedly from bacterial infections, whereas the parents and the other siblings were clinically healthy. During infectious episodes the patients showed a maculopapular skin rash, and at such times immune complexes were present in the serum. Biopsy specimens of the skin lesions showed the picture of leukocytoclastic vasculitis.
报道了一个家庭,其中11个孩子中有3个表现出C3纯合缺陷,父母和其他6个孩子的C3水平低于正常。3名患有选择性C3缺陷的儿童反复遭受细菌感染,而父母和其他兄弟姐妹临床健康。在感染发作期间,患者出现斑丘疹性皮疹,此时血清中存在免疫复合物。皮肤病变的活检标本显示白细胞破碎性血管炎的表现。