Weemaes C, Leijh P, Blussé van Oud Alblas D, van der Meer J, van Furth R
Acta Paediatr Scand. 1981;70(3):421-5. doi: 10.1111/j.1651-2227.1981.tb16578.x.
The history of a 13-year-old girl with a syndrome resembling Chronic Granulomatous Disease (C.G.D.) is described. Metabolic studies in granulocytes and monocytes classified the patient as having C.G.D. The granulocytes failed to kill Staphylococcus aureus and Candida Albicans; however, the killing of these microorganisms by the patient's monocytes was nearly normal. Family studies revealed no abnormalities in the phagocytic cells of the parents and the siblings.
本文描述了一名13岁女孩患有类似慢性肉芽肿病(C.G.D.)综合征的病史。对粒细胞和单核细胞进行的代谢研究将该患者归类为患有慢性肉芽肿病。粒细胞无法杀死金黄色葡萄球菌和白色念珠菌;然而,患者单核细胞对这些微生物的杀伤能力几乎正常。家族研究显示,父母和兄弟姐妹的吞噬细胞没有异常。