载明携带者的比率及其他在携带者筛查中意外发现

IF 4.3 4区医学 Q1 OBSTETRICS & GYNECOLOGY Obstetrical & Gynecological Survey Pub Date : 2023-07-01 DOI:10.1097/01.ogx.0000947136.14734.37

Sydney K. Clevenger, Justin S. Brandt, Shama P. Khan, Pranali Shingala, Jillian Carrick, Ruchi Aluwalia, Gary A. Heiman, Elena Ashkinadze

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引用次数: 0

摘要

(摘自prennat Diagn 2023;43:11 17 - 125)产科护理包括对母亲和婴儿的多种评估，包括遗传病筛查。这可以通过被称为携带者筛查的基因测试来完成，这种测试可以检测出有可能患有常染色体隐性遗传病和x连锁隐性遗传病的携带者。

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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Rate of Manifesting Carriers and Other Unexpected Findings on Carrier Screening

(Abstracted from Prenat Diagn 2023;43:117–125) Obstetric care includes many types of assessment of both mother and baby, including screening for genetic conditions. This can be done through genetic tests referred to as carrier screening, which detect carriers at risk to have children with autosomal recessive and X-linked recessive conditions.

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来源期刊

Obstetrical & Gynecological Survey 医学-妇产科学

CiteScore

2.70

自引率

3.20%

发文量

245

审稿时长

>12 weeks

期刊介绍： Each monthly issue of Obstetrical & Gynecological Survey presents summaries of the most timely and clinically relevant research being published worldwide. These concise, easy-to-read summaries provide expert insight into how to apply the latest research to patient care. The accompanying editorial commentary puts the studies into perspective and supplies authoritative guidance. The result is a valuable, time-saving resource for busy clinicians.