Non-invasive prenatal diagnosis and determination of fetal Rh status

被引:60
作者
van der Schoot, C. Ellen [1 ,2 ]
Hahn, Sinuhe [3 ]
Chitty, Lyn S. [4 ,5 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Landsteiner Lab, NL-1066 CX Amsterdam, Netherlands
[2] Sanquin Res, Amsterdam, Netherlands
[3] Univ Basel Hosp, Univ Womens Hosp, Dept Res, Basel, Switzerland
[4] UCL Hosp, NHS Fdn Trust, Fetal Med Unit, London, England
[5] UCL Hosp, NHS Fdn Trust, Clin & Mol Genet Unit, Inst Child Hlth, London, England
关键词
fetal RHD status; non-invasive prenatal; diagnosis; cell-free fetal DNA;
D O I
10.1016/j.siny.2007.12.012
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
RhD blood group incompatibility between a pregnant woman and her fetus can result in maternal alloimmunization and consequent haemolytic disease of the newborn (HDN) in subsequent pregnancies. The D-negative blood group is found in 15% of whites, 3-5% of black Africans, and is rare in Asians. Recent technological advances in non-invasive prenatal determination of the fetal RHD status using cell-free fetal DNA (cffDNA) have opened new avenues for the management of D-negative pregnant women. In this review applications for the high risk women, as well as potential for routine screening wilt be discussed. The use of non-invasive prenatal diagnosis and the management of other blood incompatibilities wilt also be discussed. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:63 / 68
页数:6
相关论文
共 35 条
  • [1] The genetic basis of a new partial D antigen: D-DBT
    Beckers, EAM
    Faas, BHW
    Simsek, S
    Overbeeke, MAM
    vanRhenen, DJ
    Wallace, M
    vondemBorne, AEGK
    vanderSchoot, CE
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 (03) : 720 - 727
  • [2] Noninvasive prenatal diagnosis of fetal Rhesus D - Ready for prime(r) time
    Bianchi, DW
    Avent, ND
    Costa, JM
    van der Schoot, CE
    [J]. OBSTETRICS AND GYNECOLOGY, 2005, 106 (04) : 841 - 844
  • [3] Hypermethylated RASSF1A in maternal plasma:: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis
    Chan, K. C. Allen
    Ding, Chunming
    Gerovassili, Ageliki
    Yeung, Sze W.
    Chiu, Rossa W. K.
    Leung, Tse N.
    Lau, Tze K.
    Chim, Stephen S. C.
    Chung, Grace T. Y.
    Nicolaides, Kypros H.
    Lo, Y. M. Dennis
    [J]. CLINICAL CHEMISTRY, 2006, 52 (12) : 2211 - 2218
  • [4] Improvement in fetal DNA extraction from maternal plasma. Evaluation of the NucliSens magnetic extraction system and the QlAamp DSP virus kit in comparison with the QIAamp DNA blood mini kit
    Clausen, Frederik Banch
    Krog, Grethe Risum
    Rieneck, Klaus
    Dziegiel, Morten Hanefeld
    [J]. PRENATAL DIAGNOSIS, 2007, 27 (01) : 6 - 10
  • [5] COLIN Y, 1991, BLOOD, V78, P2747
  • [6] Fetal RHD genotyping in maternal serum during the first trimester of pregnancy
    Costa, JM
    Giovangrandi, Y
    Ernault, P
    Lohmann, L
    Nataf, V
    El Halali, N
    Gautier, E
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (01) : 255 - 260
  • [7] Daniels G., 2002, HUMAN BLOOD GROUPS
  • [8] Fruetal blood group genotyping - Present and future
    Daniels, Geoff
    Finning, Kirstin
    Martin, Pete
    Summers, Jo
    [J]. CIRCULATING NUCLEIC ACIDS IN PLASMA AND SERUM IV, 2006, 1075 : 88 - 95
  • [9] Detection of fetal RHD-specific sequences in maternal plasma
    Faas, BHW
    Beuling, EA
    Christiaens, GCML
    von dem Borne, AEGK
    van der Schoot, CE
    [J]. LANCET, 1998, 352 (9135) : 1196 - 1196
  • [10] Molecular background of VS and weak C expression in blacks
    Faas, BHW
    Beckers, EAM
    Wildoer, P
    Ligthart, PC
    Overbeeke, MAM
    Zondervan, HA
    vondemBorne, AEGK
    vanderSchoot, CE
    [J]. TRANSFUSION, 1997, 37 (01) : 38 - 44