Genetic Carrier Screening in the Twenty-first Century

被引:12
|
作者
Yao, Ruofan [1 ]
Goetzinger, Katherine R. [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Obstet Gynecol & Reprod Med, 22 S Greene St, Baltimore, MD 21201 USA
关键词
Ashkenazi Jewish; Carrier screening; Cystic fibrosis; Spinal muscular atrophy; Tay-Sachs disease; TAY-SACHS-DISEASE; PRENATAL-DIAGNOSIS; CFTR GENE; JEWISH; MUTATIONS; HEXOSAMINIDASE; PSEUDODEFICIENCY; IDENTIFICATION; STATEMENT; COMMON;
D O I
10.1016/j.cll.2016.01.003
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Historically, carrier screening for a small number of autosomal recessive disorders has been offered to targeted populations based on ethnicity and family history. These chosen disorders are associated with severe morbidity or mortality, have a well-established carrier frequency in the targeted population, and have an acceptably high detection rate to make screening efficient. With advancing genetic technology, expanded panels rapidly are being designed and offered to the panethnic general population. This article reviews current recommendations for ethnicity specific carrier screening for common disorders as well as the limitations and counseling complexities associated with expanded panels.
引用
收藏
页码:277 / +
页数:14
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