隐性遗传疾病的夫妻筛查。

IF 2.6 4区 医学 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Journal of Medical Screening Pub Date : 2023-06-01 DOI:10.1177/09691413221137039
Silvina Sisterna, Antoni Borrell
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引用次数: 0

摘要

夫妇筛查的目的是识别孩子患有常染色体隐性遗传病或x连锁疾病的风险增加的夫妇,以促进知情的生殖决策。准父母双方应该作为一个整体进行筛查,而不是单独进行检测。携带者检测通常是针对一些相对常见的隐性疾病进行的,这些疾病与显著发病率、预期寿命缩短有关,而且往往是因为特定人群中某些疾病的携带者频率相当高。然而,新的基因检测技术使筛选扩大到多种条件,基因和序列变异。筛查有风险的夫妇有多种生殖选择,特别是在孕前阶段检测到遗传特征时。
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Couple screening for recessively inherited disorders.

Couple screening aims to identify couples with an increased risk of having a child affected with an autosomal recessive or X-linked disorder, in order to facilitate informed reproductive decision making. Both expectant parents should be screened as a single entity, instead of individual testing. Carrier testing was typically performed for a few relatively common recessive disorders associated with significant morbidity, reduced life expectancy and often because of a considerably higher carrier frequency in a specific population for certain diseases. However, new genetic testing technologies enable the expansion of screening to multiple conditions, genes and sequence variants. There are multiple reproductive options for screening couples at risk, particularly when genetic traits are detected in the preconception period.

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来源期刊
Journal of Medical Screening
Journal of Medical Screening 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.90
自引率
3.40%
发文量
40
审稿时长
>12 weeks
期刊介绍: Journal of Medical Screening, a fully peer reviewed journal, is concerned with all aspects of medical screening, particularly the publication of research that advances screening theory and practice. The journal aims to increase awareness of the principles of screening (quantitative and statistical aspects), screening techniques and procedures and methodologies from all specialties. An essential subscription for physicians, clinicians and academics with an interest in screening, epidemiology and public health.
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