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A retrospective study of paediatric health and development following pre-implantation genetic diagnosis and screening

机译:植入前遗传诊断和筛查后小儿健康和发育的回顾性研究

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Pre-implantation genetic diagnosis and screening (PGD and PGS) are treatments for patients that have (or are carriers of) an inherited genetic disorder, or who have had a history of miscarriage, problems with embryo implantation, etc. Often conducted alongside assisted reproductive technologies (ART), a number of embryos are produced, and the DNA and chromosomes of each are tested for various disorders by removing one or two cells for analysis. A retrospective cross-sectional study looking at the health and development of children born following PGD and PGS is now underway, aided by an online system developed by the EuroPGDcode project. Data has been collected from a number of ART/PGD centres worldwide, and has been entered into this system. A number of complex queries have been constructed to interrogate the data; although retrospective and not case controlled, indications are that the birth abnormality rate is low at 1.42%. However the special care requirements of PGD infants was 22.9% and the incidence of health problems after birth was 22.3%. In addition to statistical analysis of the data, a number of cases of particular interest have been identified. The online system provides the facility for the full details of these cases to be exported in a specially designed XML format for further analysis.
机译:植入前遗传诊断和筛选(PGD和PGS)是对遗传遗传性疾病(或是携带者)的患者的治疗,或者患有流产史,胚胎植入史等的患者通常与辅助生殖一起进行技术(技术),产生多种胚胎,并且通过除去一个或两个细胞进行各种疾病来测试各种疾病的DNA和染色体。目前正在进行看着PGD和PGS之后出生的儿童健康和发展的回顾性横断面研究,并通过Europgdcode项目开发的在线系统。已从全球许多艺术/ PGD中心收集数据,并已进入该系统。已经构建了许多复杂的查询以询问数据;虽然回顾性而非案例控制,迹象表明,出生异常率低1.42%。然而,PGD婴儿的特殊护理要求是22.9%,出生后的健康问题发生率为22.3%。除了对数据的统计分析外,还确定了许多特别令人兴趣的情况。在线系统提供了这些情况的完整细节,以便以特殊设计的XML格式导出以进行进一步分析。

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