Rapid aneuploidy screening (FISH or QF-PCR): the changing scene in prenatal diagnosis?

被引:23
作者
Leung, WC [1 ]
Lau, ET
Lao, TT
Tang, MH
机构
[1] Univ Hong Kong, Queen Mary Hosp, Prenatal Diagnost & Counselling Dept, Tsan Yuk Hosp,Dept Obstet & Gynecol, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Tsan Yuk Hosp, Prenatal Diagnost & Counselling Dept, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Queen Mary Hosp, Dept Obstet & Gynecol, Hong Kong, Hong Kong, Peoples R China
关键词
amniocentesis; FISH; prenatal diagnosis; QF-PCR; rapid aneuploidy screening;
D O I
10.1586/14737159.4.3.333
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The accuracy new molecular diagnostics, fluoresence in situ hybridization or quantitative fluorescence-PCR (collectively known as rapid aneuploidy screening), in prenatal diagnosis has already been demonstrated in a number of large studies. The challenge now is how to apply them clinically in the most cost-effective manner. It is now replace traditional karyotyping time to appraise whether rapid aneuploidy screening can re when amniocenteses are performed for increased risk of Down's syndrome by maternal serum screening or advanced maternal age in the absence of ultrasound abnormality. The ten most recent studies from the literature within this research theme are reviewed and the pros and cons of this new approach in prenatal diagnosis are discussed, including the suggestion of future studies.
引用
收藏
页码:333 / 337
页数:5
相关论文
共 24 条
[1]   Prenatal detection of chromosome disorders by QF-PCR [J].
Adinolfi, M ;
Sherlock, J .
LANCET, 2001, 358 (9287) :1030-1031
[2]   Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization -: Evaluation of >3,000 cases [J].
Eiben, B ;
Trawicki, W ;
Hammans, W ;
Goebel, R ;
Pruggmayer, M ;
Epplen, JT .
FETAL DIAGNOSIS AND THERAPY, 1999, 14 (04) :193-197
[3]  
Estabrooks LL, 1999, AM J HUM GENET, V65, pA162
[4]   International, collaborative assessment of 146 000 prenatal karyotypes: expected limitations if only chromosome-specific probes and fluorescent in-situ hybridization are used [J].
Evans, MI ;
Henry, GP ;
Miller, WA ;
Bui, TH ;
Snidjers, RJ ;
Wapner, RJ ;
Miny, P ;
Johnson, MP ;
Peakman, D ;
Johnson, A ;
Nicolaides, K ;
Holzgreve, W ;
Ebrahim, SAD ;
Babu, R ;
Jackson, L .
HUMAN REPRODUCTION, 1999, 14 (05) :1213-1216
[5]  
Grimshaw G M, 2003, Health Technol Assess, V7, P1
[6]   Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH) [J].
Homer, J ;
Bhatt, S ;
Huang, B ;
Thangavelu, M .
PRENATAL DIAGNOSIS, 2003, 23 (07) :566-571
[7]   The effect of fast reporting by amnio-PCR on anxiety levels in women with positive biochemical screening for Down syndrome - a randomized controlled trial [J].
Leung, WC ;
Lam, YH ;
Wong, Y ;
Lau, ET ;
Tang, MHY .
PRENATAL DIAGNOSIS, 2002, 22 (03) :256-259
[8]   Can amnio-polymerase chain reaction alone replace conventional cytogenetic study for women with positive biochemical screening for fetal Down syndrome? [J].
Leung, WC ;
Lau, ET ;
Lao, TT ;
Tang, MHY .
OBSTETRICS AND GYNECOLOGY, 2003, 101 (05) :856-861
[9]  
Leung WC, 2001, PRENATAL DIAG, V21, P327
[10]   A large-scale evaluation of amnio-PCR for the rapid prenatal diagnosis of fetal trisomy [J].
Levett, LJ ;
Liddle, S ;
Meredith, R .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2001, 17 (02) :115-118