Suppr超能文献

家族性自主神经功能异常的植入前基因诊断

Preimplantation genetic diagnosis for familial dysautonomia.

作者信息

Rechitsky S, Verlinsky O, Kuliev A, Ozen R S, Masciangelo C, Lifchez A, Verlinsky Y

机构信息

Reproductive Genetics Institute, Chicago, IL 60657, USA.

出版信息

Reprod Biomed Online. 2003 Jun;6(4):488-93. doi: 10.1016/s1472-6483(10)62172-4.

Abstract

Familial dysautonomia (FD) is the most common congenital sensory neuropathy in Ashkenazi Jews, caused by a single major mutation in the IKBKAP gene. Effective management for this severe debilitating disease is still not available, making preimplantation genetic diagnosis (PGD) a useful option for at-risk couples to establish an FD free pregnancy from the outset. PGD was performed for a couple with a previous affected child with FD, using first and second polar body testing to preselect mutation-free oocytes, based on mutation analysis with simultaneous testing of two closely linked markers, D9S58 and D9S1677. Of 15 tested oocytes, 11 carried information about both polar bodies' genotype, of which seven were predicted to be free of the FD gene. Three embryos resulting from these oocytes were transferred back to the patient, resulting in a triplet pregnancy and the birth of three unaffected children confirmed to be free of FD. This is the first PGD for FD, providing an alternative for those at-risk couples who cannot accept prenatal diagnosis and termination of pregnancy as an option for avoiding FD.

摘要

家族性自主神经功能障碍(FD)是阿什肯纳兹犹太人中最常见的先天性感觉神经病,由IKBKAP基因的单一主要突变引起。对于这种严重致残性疾病,目前仍没有有效的治疗方法,这使得植入前基因诊断(PGD)成为有风险的夫妇从一开始就孕育无FD胎儿的有用选择。对一对曾生育过一名患FD患儿的夫妇进行了PGD,基于对两个紧密连锁标记D9S58和D9S1677的同时检测进行突变分析,采用第一极体和第二极体检测来预选无突变的卵母细胞。在15个检测的卵母细胞中,11个携带了两个极体基因型的信息,其中7个预计不含FD基因。由这些卵母细胞产生的3个胚胎被移植回患者体内,结果是三胎妊娠,3个未受影响的孩子出生,经确认无FD。这是首例针对FD的PGD,为那些无法接受产前诊断和终止妊娠以避免FD的有风险夫妇提供了一种选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验