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基于分子技术的阿什肯纳兹犹太遗传病产前筛查经验。

Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases.

作者信息

Eng C M, Desnick R J

机构信息

Department of Human Genetics, Mount Sinai School of Medicine of New York University New York 10029, USA.

出版信息

Adv Genet. 2001;44:275-96. doi: 10.1016/s0065-2660(01)44086-7.

Abstract

Multiple-option prenatal carrier testing in the Ashkenazi Jewish community for three and now eight disorders has been readily accepted in this prenatal, health-oriented and knowledgeable population. Counseling of screenees concerning the nature (severity, treatability, etc.), inheritance, and frequencies of each disorder was essential for informed test choices and future reproductive decision making. The value of couple testing for a group of disorders when 1 in about 6 would be found to be a carrier of at least one disease was emphasized. These studies identified issues of education, confidentiality, posttest anxiety, and self-esteem that must be continuously addressed in the Ashkenazi population. However, an important value of these studies is that they provide a framework for the development of mass carrier screening programs in the general population or in specific segments of the population with similar demographic characteristics and in more diverse prenatal populations.

摘要

在阿什肯纳兹犹太人群体中,针对三种(现在是八种)疾病进行的多选项产前携带者检测,已被这个注重产前健康且知识丰富的群体欣然接受。就每种疾病的性质(严重程度、可治疗性等)、遗传方式和发病率,向受检者提供咨询,对于做出明智的检测选择和未来的生育决策至关重要。当发现约六分之一的人至少携带一种疾病的致病基因时,对一组疾病进行夫妻双方检测的价值得到了强调。这些研究确定了教育、保密、检测后焦虑和自尊等问题,在阿什肯纳兹人群体中必须持续关注这些问题。然而,这些研究的一个重要价值在于,它们为在普通人群、具有相似人口特征的特定人群细分群体以及更多样化的产前人群中开展大规模携带者筛查项目提供了框架。

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