Lee S H, Kwak I P, Cha K E, Park S E, Kim N K, Cha K Y
Pochon CHA University Medical College, Department of Obstetrics and Gynecology, CHA General Hospital Korea, Seoul.
Mol Hum Reprod. 1998 Apr;4(4):345-9. doi: 10.1093/molehr/4.4.345.
The use of preimplantation diagnosis for sex determination and detection of exon deletion means that unaffected babies can be born to parents suffering from Duchenne muscular dystrophy (DMD). However, those who do not have exon deletion should also be considered for further investigation. A new method, known as linkage analysis, has been developed to diagnose the presence of non-deletion DMD in preimplantation embryos. Linkage analysis uses informative intragenic and flanking markers to track the chromosome bearing the mutated gene. The present study reports the analysis of two polymorphic sites, in blastomeres biopsied from embryos from a female carrier of DMD. A single male embryo was obtained who had inherited alternate maternal alleles to the woman's affected surviving son, and this embryo was transferred.
利用植入前诊断进行性别鉴定和外显子缺失检测,这意味着患有杜氏肌营养不良症(DMD)的父母能够生育未受影响的婴儿。然而,对于那些没有外显子缺失的情况,也应考虑进行进一步检查。一种名为连锁分析的新方法已被开发出来,用于诊断植入前胚胎中是否存在非缺失型DMD。连锁分析利用信息性基因内和侧翼标记来追踪携带突变基因的染色体。本研究报告了对来自一名DMD女性携带者胚胎活检的卵裂球中两个多态性位点的分析。获得了一个单男性胚胎,其继承了与该女性受影响的存活儿子不同的母本等位基因,随后将该胚胎进行了移植。