Asch D A, Patton J P, Hershey J C, Mennuti M T
Division of General Internal Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104-2676.
Am J Obstet Gynecol. 1993 Jan;168(1 Pt 1):1-6. doi: 10.1016/s0002-9378(12)90875-3.
The recent discovery of the cystic fibrosis gene has offered the possibility of population-based cystic fibrosis carrier screening. Although > 100 distinct mutations have been identified, five of these in aggregate represent about 85% of the alleles in Britain and the United States. Screening programs that test for these five mutations can be designed to offer several alternative ways to communicate the risk to a pregnancy and several alternative ways to manage a pregnancy. At this time we favor a strategy of screening partners in a couple in sequence, screening the second partner only if the first is positive; nevertheless, different strategies will appeal to different couples.
最近囊性纤维化基因的发现为基于人群的囊性纤维化携带者筛查提供了可能性。尽管已鉴定出100多种不同的突变,但其中5种突变加起来约占英国和美国等位基因的85%。检测这5种突变的筛查项目可以设计出几种向孕妇传达风险的替代方法,以及几种处理妊娠的替代方法。目前,我们倾向于一种依次筛查夫妻中一方的策略,只有当第一个人检测结果为阳性时才对第二个人进行筛查;然而,不同的策略会吸引不同的夫妻。