Patrone F, Dallegri F, Rebora A
Eur J Pediatr. 1979 Mar 1;130(3):181-7. doi: 10.1007/BF00455264.
An 11-year-old boy with a life-long history of atopic-like dermatitis and recurrent staphylococcal abscesses was found to have defective neutrophil chemotaxis, impaired-T-lymphocyte functions, hyperimmunoglobulinemia E, and delayed neutrophil bactericidal power. This latter defect has never been found in such patients. The patient's mother revealed a panhypogammaglobulinemia, while his sister and maternal grandmother who had repeated infections were immunologically normal.
一名11岁男孩，有终生特应性皮炎样病史和复发性葡萄球菌脓肿，被发现存在中性粒细胞趋化功能缺陷、T淋巴细胞功能受损、免疫球蛋白E升高以及中性粒细胞杀菌能力延迟。后一种缺陷在这类患者中从未被发现。患者的母亲表现为全血细胞减少性低丙种球蛋白血症，而他有反复感染病史的姐姐和外祖母免疫功能正常。
