Rosatelli M C, Tuveri T, Scalas M T, Di Tucci A, Leoni G B, Furbetta M, Monni G, Cao A
Istituto di Clinica e Biologia dell'Età Evolutiva, Università degli Studi di Cagliari, Sardinia.
J Med Genet. 1988 Nov;25(11):762-5. doi: 10.1136/jmg.25.11.762.
We have used four oligonucleotide probes and two restriction enzymes to detect the beta thalassaemia mutation in a group of 61 couples of Italian descent who were prospective parents. We have been able to define the beta thalassaemia mutation in both parents in 47 couples and in only one parent in 12 couples. Prenatal diagnosis was accomplished successfully either by amniocyte (two) or trophoblast (26) DNA analysis in 28 couples in which the pregnancy was in progress. These results indicate that direct identification of the mutation by oligonucleotide or restriction endonuclease analysis is a practical and useful method for prenatal diagnosis of beta thalassaemia in childless couples.
我们使用了四种寡核苷酸探针和两种限制性内切酶,对61对有意大利血统的准父母进行β地中海贫血突变检测。我们已能够确定47对夫妇双方的β地中海贫血突变,以及12对夫妇中仅一方的突变。在28对正在妊娠的夫妇中,通过羊水细胞(2例)或滋养层细胞(26例)DNA分析成功完成了产前诊断。这些结果表明,通过寡核苷酸或限制性内切酶分析直接鉴定突变,对于无子女夫妇的β地中海贫血产前诊断是一种实用且有效的方法。