Current controversies in prenatal diagnosis 4: pre-conception expanded carrier screening should replace all current prenatal screening for specific single gene disorders

被引:18
作者
Langlois, Sylvie [1 ]
Benn, Peter [2 ]
Wilkins-Haug, Louise [3 ]
机构
[1] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[2] Univ Connecticut, Ctr Hlth, Div Human Genet, Farmington, CT USA
[3] Brigham & Womens Hosp, Div Div Maternal Fetal Med, Boston, MA 02115 USA
关键词
GYNECOLOGISTS; THALASSEMIA; PREVENTION; VARIANTS;
D O I
10.1002/pd.4532
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
What's already known about this topic?In the United States there is increasing availability of pan-ethnic carrier screening covering mutations in a large number of genes ("expanded screening").A large-scale study on the use of expanded carrier screening has been published by a commercial laboratory offering this test.The American College of Medical Genetics and Genomics has issued a position statement on prenatal/preconception expanded carrier screening. What does the study add?This report summarizes an oral debate presented at the 18th International Conference on Prenatal Diagnosis and Therapy in Brisbane, Australia on 23 July 2014.The benefits, limitations, and challenges of preconception expanded carrier screening are discussed. © 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:23 / 28
页数:6
相关论文
共 30 条
  • [21] Mosher W. D., 2012, NATL HLTH STAT REPOR, V55, P1
  • [22] Passel JS, 2010, PEW SOCIAL TREN 0615
  • [23] Carrier screening for spinal muscular atrophy
    Prior, Thomas W.
    [J]. GENETICS IN MEDICINE, 2008, 10 (11) : 340 - 342
  • [24] Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population
    Rohlfs, Elizabeth M.
    Zhou, Zhaoqing
    Heim, Ruth A.
    Nagan, Narasimhan
    Rosenblum, Lynne S.
    Flynn, Kerry
    Scholl, Thomas
    Akmaev, Viatcheslav R.
    Sirko-Osadsa, D. Alexa
    Allitto, Bernice A.
    Sugarman, Elaine A.
    [J]. CLINICAL CHEMISTRY, 2011, 57 (06) : 841 - 848
  • [26] Considering the cost of expanded carrier screening panels
    Stoll, Katie
    Resta, Robert
    [J]. GENETICS IN MEDICINE, 2013, 15 (04) : 318 - 319
  • [27] The dangers of including nonclassical cystic fibrosis variants in population-based screening panels: p.L997F, further genotype/phenotype correlation data
    Strom, Charles M.
    Redman, Joy B.
    Peng, Mei
    [J]. GENETICS IN MEDICINE, 2011, 13 (12) : 1042 - 1044
  • [28] EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies
    Traeger-Synodinos, Joanne
    Harteveld, Cornelis L.
    Old, John M.
    Petrou, Mary
    Galanello, Renzo
    Giordano, Piero
    Angastioniotis, Michael
    De la Salle, Barbara
    Henderson, Shirley
    May, Alison
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23 (04) : 426 - 437
  • [29] UK National Screening Committee, UK NSC POL DAT
  • [30] Wilson R Douglas, 2002, J Obstet Gynaecol Can, V24, P644