...
首页> 外文期刊>Neurology India >Molecular Genetics involved in Neural Tube Defects: Recent Advances and Future Prospective for Molecular Medicine
【24h】

Molecular Genetics involved in Neural Tube Defects: Recent Advances and Future Prospective for Molecular Medicine

机译:参与神经管缺陷的分子遗传学:最近的进展和未来的分子医学前瞻性

获取原文

摘要

Background: Folic acid and multivitamin supplements ((FAMVS) and genetics involvement is one of the major roles in the development of neural tube defects (NTDs). Objective: Our prior aim and objective is to establish an unique guideline and helps the policy decision making for our country India and the World. Materials and Methods: We have collected the data through the literature from the World for their necessary action, rehabilitation part all objectively in PubMed/Medline, Scopous, Embase, Cochrane Review, Hinari, and Google scholar. Statistical Analysis: Statistical analysis was performed with very simple and logistic statistics, percentage, mean, total as collection through the available software SPSS with new version 17.0. Results: The overall (70-95%) we find out those infants with neural tube defects (NTDs) associated with genes involvement and maternal vitamin intake (MVI). Before pregnancy relative risk (PRR) prior to non intake noted as 90% significantly reduced their risk of the NTDs. Now (40-60%) of the women of child-bearing age (CBA) don't use the folic acid intake and supplements (FAISs) in proper way in villages, urban, industrial and sewage areas. We find out that the genetic variants of the fourteen special reported genes, had the major risk factor (MRF) for the (NTDs) and associated abnormalities rate (AAR) within the developmental process in the human brain. Conclusions: The (45-55%) people still having at ignorant zone, due to lack of education, genetic counseling, and awareness till date.
机译:背景:叶酸和多种维生素补充剂((FAMV)和遗传学受累是神经管缺陷发展(NTDS)的主要作用之一。目的:我们的先前目的是建立独特的指导并帮助政策决策对于我国印度和世界。材料和方法:我们通过世界的文献收集了这些数据,以获得必要的行动,康复部分在被困/美德,突发,博览会,辛巴里和谷歌学者中。统计分析:通过具有新版本17.0的可用软件SPS,以非常简单和逻辑统计,百分比,百分比,总计进行统计分析,百分比,总计。结果:总体(70-95%)我们发现了那些具有神经管缺陷的婴儿(NTDS)与基因受累和母体维生素摄入(MVI)相关联。在非摄入前的妊娠相对风险(PRR)之前指出,90%显着降低了风险NTDS。现在(40-60%)患有育龄年龄(CBA)的女性在村庄,城市,工业和污水区的适当方式中不要使用叶酸摄入和补充剂(Faiss)。我们发现十四个特别报告的基因的遗传变异,在人脑的发育过程中具有(NTDS)和相关异常率(AAR)的主要危险因素(MRF)。结论:由于缺乏教育,遗传咨询和意识,仍然具有无知区的(45-55%)人们仍然存在于忽视区。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号