Síndrome de Down hereditario poco común debido a la translocación robertsoniana 15/21: asesoramiento genético y reproductivoa

L.M. Azevedo Moreira, L. Damasceno Espirito Santo, A. Fernandes Lacerda Carvalho
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引用次数: 0

Abstract

The carriers of a rearrangement involving with chromosome 21 have a potential risk of genetically unbalanced conceptions, which may result in liveborn children with Down syndrome. Reproductive risks for couples carriers of a balanced Robertsonian translocation depends on the rearranged chromosomes and the sex of the carrier. This article aims to analyze the segregation and reproductive trend of a rare 15/21 translocation in five generations of a family. It was considered the current advances in reproductive technology as a possibility to prevent fetal aneuploidia. Given the genetic risk, the preimplantation diagnosis appears also as an alternative to avoid the option of an unwanted later abortion and to obtain a healthy progeny.

罗伯逊易位引起的罕见遗传性唐氏综合征15/21:遗传咨询和生殖a
21号染色体重排的携带者有潜在的基因不平衡受孕的风险,这可能导致活产的孩子患有唐氏综合症。携带平衡罗伯逊易位的夫妇的生殖风险取决于重排的染色体和携带者的性别。本文旨在分析一个家族五代罕见的15/21易位的分离和繁殖趋势。人们认为当前生殖技术的进步有可能预防胎儿非整倍体。考虑到遗传风险,植入前诊断似乎也是一种选择,以避免不想要的后来堕胎的选择,并获得健康的后代。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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