BIRTH OF HEALTHY NEONATE FOLLOWING PREIMPLANTATION GENETIC DIAGNOSIS IN A MOTHER WITH MOSAIC TURNER SYNDROME. CASE REPORT AND REVIEW OF THE LITERATURE.

Q3 Medicine
Walter Osorio-Ramírez, Juan Giraldo-Moreno, Diana Gómez-Cortés, David Olive, John Cano-Franco, Sergio Tamayo-Hussein
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引用次数: 1

Abstract

Objective: To report the case of a patient with mosaic Turner syndrome who underwent assisted reproduction treatment with preimplantation genetic testing for aneuploidy and gave birth to a healthy baby girl with normal karyotype; and to conduct a review of the literature on the usefulness of preimplantation genetic diagnosis in women with Turner syndrome.

Methods: A case of a 27 year-old woman diagnosed with mosaic Turner syndrome and secondary altered ovarian reserve, seen in a referral center for infertility management in Medellín, Colombia. The patient underwent in vitro fertilization followed by pre-implantation genetic testing to prevent transmission of Turner syndrome to her progeny. A literature search was conducted in the Medline via PubMed, Clinical Key, OVID, Embase, Lilacs, SciELO and Oxford Journals databases using the following terms: "Turner Syndrome," "Mosaic Turner," "Preimplantation Genetic Screening," "Preimplantation Genetic Testing," "Preimplantation Genetic Diagnosis," "Pregnancy," "Successful pregnancy." Inclusion criteria were case series and case reports, cohort studies and review articles published between January 1980 and June 2017 that included women with Turner syndrome achieving pregnancy by means of in vitro fertilization techniques with their own oocytes and who had undergone embryo biopsy for preimplantation genetic diagnosis. The search was limited to articles in Spanish and English.

Results: one study met the inclusion criteria. Both in this report and in our case, patients with mosaic Turner syndrome underwent several cycles of intracytoplasmic sperm injection (ICSI) with their own eggs, then performed embryonic biopsy for preimplantation genetic analysis using different techniques. In both cases, euploid embryos were transferred to the uterus with the subsequent birth of healthy girls with normal karyotype.

Conclusions: Patients with mosaic Turner syndrome could benefit from preimplantation biopsy and genetic analysis to prevent transmission of the genetic defect to their progeny.

一个患有马赛克特纳综合征的母亲的胚胎植入前遗传学诊断后健康新生儿的出生。病例报告及文献复习。
目的:报道1例马赛克特纳综合征患者接受非整倍体植入前基因检测辅助生殖治疗,生下正常核型的健康女婴;并对胚胎植入前遗传学诊断对特纳综合征妇女的有用性进行文献回顾。方法:一个27岁的妇女诊断为马赛克特纳综合征和继发性改变卵巢储备,看到在转诊中心不孕症管理Medellín,哥伦比亚。患者接受了体外受精,随后进行了植入前基因检测,以防止特纳综合征传播给她的后代。通过PubMed、Clinical Key、OVID、Embase、Lilacs、SciELO和Oxford Journals数据库在Medline进行文献检索,使用以下术语:“Turner综合征”、“Mosaic Turner”、“着床前遗传学筛查”、“着床前遗传学检测”、“着床前遗传学诊断”、“妊娠”、“成功妊娠”。纳入标准是1980年1月至2017年6月期间发表的病例系列和病例报告、队列研究和综述文章,其中包括通过自身卵母细胞体外受精技术实现妊娠的特纳综合征妇女,并接受胚胎活检进行植入前遗传学诊断。搜索仅限于西班牙语和英语的文章。结果:1项研究符合纳入标准。在本报告和我们的病例中,患有马赛克特纳综合征的患者都用自己的卵子进行了几个周期的卵胞浆内单精子注射(ICSI),然后使用不同的技术进行胚胎活检以进行着床前遗传学分析。在这两种情况下,整倍体胚胎被移植到子宫,随后出生的是核型正常的健康女孩。结论:镶嵌特纳综合征患者可以通过植入前活检和遗传分析来预防遗传缺陷的遗传。
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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来源期刊
Revista Colombiana de Obstetricia y Ginecologia
Revista Colombiana de Obstetricia y Ginecologia Medicine-Obstetrics and Gynecology
CiteScore
1.00
自引率
0.00%
发文量
21
审稿时长
20 weeks
期刊介绍: The Revista Colombiana de Obstetricia y Ginecología was founded in January 1949. It is the Federación Colombiana de Asociaciones de Obstetricia y Ginecología"s official periodic publication (formerly known as the Sociedad Colombiana de Obstetricia y Ginecología). It is published quarterly and the following abbreviation should be used when citing the journal: Rev. Colomb. Obstet. Ginecol. The publication is authorized by Mingobierno resolution 218/1950.
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