Expanded Carrier Screening in Reproductive Medicine-Points to Consider A Joint Statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine

被引:277
作者
Edwards, Janice G.
Feldman, Gerald
Goldberg, James
Gregg, Anthony R.
Norton, Mary E.
Rose, Nancy C.
Schneider, Adele
Stoll, Katie
Wapner, Ronald
Watson, Michael S.
机构
[1] Amer Coll Med Genet & Genom, Bethesda, MD USA
[2] Amer Coll Obstetricians & Gynecologists, Washington, DC 20024 USA
[3] Soc Maternal Fetal Med, Washington, DC USA
[4] Natl Soc Genet Counselors, Chicago, IL USA
[5] Perinatal Qual Fdn, Oklahoma City, OK USA
关键词
PRACTICE GUIDELINES; HEMOCHROMATOSIS; MUTATIONS;
D O I
10.1097/AOG.0000000000000666
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The Perinatal Quality Foundation and the American College of Medical Genetics and Genomics, in association with the American College of Obstetricians and Gynecologists, the Society for Maternal-Fetal Medicine, and the National Society of Genetic Counselors, have collaborated to provide education for clinicians and laboratories regarding the use of expanded genetic carrier screening in reproductive medicine. This statement does not replace current screening guidelines, which are published by individual organizations to direct the practice of their constituents. As organizations develop practice guidelines for expanded carrier screening, further direction is likely. The current statement demonstrates an approach for health care providers and laboratories who wish to or who are currently offering expanded carrier screening to their patients.
引用
收藏
页码:653 / 662
页数:10
相关论文
共 22 条
[1]   HFE-associated hereditary hemochromatosis [J].
Alexander, Jacob ;
Kowdley, Kris V. .
GENETICS IN MEDICINE, 2009, 11 (05) :307-313
[2]  
American College of Obstetricians and Gynecologists, 2009, OBSTET GYNECOL, V113, P1194
[3]  
American College of Obstetricians and Gynecologists Committee on Genetics, 2011, OBSTET GYNECOL, V117, P1028, DOI [DOI 10.1097/AOG.0B013E31821922C2, 10.1097/AOG.0b013e31821922c2]
[4]  
[Anonymous], OBSTET GYNECOL
[5]  
[Anonymous], 2010, OBSTET GYNECOL, V116, P1008
[6]  
[Anonymous], 2007, OBSTET GYNECOL, DOI DOI 10.1097/00006250-200701000-00055
[7]  
Botto LD, 2000, AM J EPIDEMIOL, V151, P862
[8]   Screening for hemochromatosis: Recommendation statement [J].
Calonge, Ned ;
Petitti, Diana B. ;
DeWitt, Thomas G. ;
Gordis, Leon ;
Gregory, Kimberly D. ;
Harris, Russell ;
Kizer, Kenneth W. ;
LeFevre, Michael L. ;
Loveland-Cherry, Carol ;
Marion, Lucy N. ;
Moyer, Virginia A. ;
Ockene, Judith K. ;
Sawaya, George F. ;
Siu, Albert L. ;
Teutsch, Steven M. ;
Yawn, Barbara P. .
ANNALS OF INTERNAL MEDICINE, 2006, 145 (03) :204-208
[9]   Expanded carrier screening in reproductive healthcare: perspectives from genetics professionals [J].
Cho, D. ;
McGowan, M. L. ;
Metcalfe, J. ;
Sharp, R. R. .
HUMAN REPRODUCTION, 2013, 28 (06) :1725-1730
[10]  
Finucane B, 2012, J GENET COUNS, V21, P752, DOI 10.1007/s10897-012-9524-8