Hitzig W H, Seger R A
Hum Genet. 1983;64(3):207-15. doi: 10.1007/BF00279395.
Chronic granulomatous disease (CGD) is a clinical syndrome, the unifying characteristics of which are a severe predisposition to bacterial and fungal infections, an impaired ability of phagocytic leukocytes to kill certain microorganisms and the failure of these cells to produce microbicidal oxygen metabolites. In CGD the causal biochemical defect and the mechanism of genetic transmission vary from family to family. At least six different molecular defects have been found to underly the X-linked and at least three other the autosomal recessive form of CGD. Diagnosis of carriers is possible in most instances, and prenatal diagnosis by fetoscopic placental vessel puncture has become feasible.
慢性肉芽肿病(CGD)是一种临床综合征,其共同特征是极易发生细菌和真菌感染、吞噬性白细胞杀灭某些微生物的能力受损以及这些细胞无法产生杀菌性氧代谢产物。在慢性肉芽肿病中,致病的生化缺陷和遗传传递机制因家族而异。已发现至少六种不同的分子缺陷是X连锁慢性肉芽肿病的基础,至少还有三种是常染色体隐性形式慢性肉芽肿病的基础。在大多数情况下可以诊断携带者,通过胎儿镜胎盘血管穿刺进行产前诊断已变得可行。