In-house genetic counseling increases the detection of abnormal karyotypes—a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland

被引:0
作者
Julia Bijok
Anna Kucińska–Chahwan
Diana Massalska
Alicja Ilnicka
Grzegorz Panek
Tomasz Roszkowski
机构
[1] Centre of Postgraduate Medical Education,Department of Gynecologic Oncology and Obstetrics
[2] Institute of Psychiatry and Neurology,Genetic Department
来源
Journal of Assisted Reproduction and Genetics | 2020年 / 37卷
关键词
Changing patterns; Chromosomal anomalies; Genetic counseling; Genetic screening; Indications; Prenatal diagnosis;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:1999 / 2006
页数:7
相关论文
共 116 条
[1]  
Lejeune J(1959)Study of somatic chromosomes from 9 mongoloid children C R Hebd Seances Acad Sci. 248 1721-1722
[2]  
Gautier M(1966)Chromosome analysis of human amniotic – fluid cells Lancet 1 383-385
[3]  
Turpin R(1987)Screening for Down’s syndrome using an iso-risk curve based on maternal age and serum alpha-fetoprotein level Br J Obstet Gynaecol. 94 636-642
[4]  
Steele M(1987)Estimating a woman’s risk of having a pregnancy associated with Down’s syndrome using her age and serum alpha-fetoprotein level Br J Obstet Gynaecol. 94 387-402
[5]  
Berg WJ(2011)Trends in the utilization of invasive prenatal diagnosis in The Netherlands during 2000-2009 Prenat Diagn. 31 765-772
[6]  
Tabor A(2014)Evaluation of the introduction of the national Down syndrome screening program in the Netherlands: age-related uptake of prenatal screening and invasive diagnostic testing Eur J Obstet Gynecol Reprod Biol. 174 59-63
[7]  
Larsen SO(2016)Changing indications for invasive testing in an era of improved screening Semin Perinatol. 40 56-66
[8]  
Nielsen J(2004)Changes in the utilization of prenatal diagnosis Obstet Gynecol. 103 1255-1260
[9]  
Cuckle HS(2015)Changes in and efficacies of indications for invasive prenatal diagnosis of cytogenomic abnormalities: 13 years of experience in a single center Med Sci Monit. 21 1942-1948
[10]  
Wald NJ(2015)National decline in invasive prenatal diagnostic procedures in association with uptake of combined first trimester and cell-free DNA aneuploidy screening Aust N Z J Obstet Gynaecol. 55 507-510