论文部分内容阅读
已报道的囊性纤维化(CF)杂合子患者除了气道反应性增高外,临床并无异常。CF 基因的发现促使作者在慢性支气管过度分泌患者中检测了CFΔF508携带者.对65例年龄27～67岁的持续性或间歇性支气管漏患者进行了探讨.其中6例患者为ΔF508缺乏的杂合
Reported cystic fibrosis (CF) heterozygous patients in addition to increased airway reactivity, the clinical no exception. The discovery of the CF gene prompted the authors to examine CFΔF508 carriers in patients with chronic bronchial hypersecretion.65 patients with persistent or intermittent bronchial leaks aged 27-67 years were studied, 6 of whom were heterozygous for ΔF508 deficiency