Literature DB >> 14607035

Fatal hydrops fetalis caused by anti-D in a mother with partial D.

Michael Cannon1, Richard Pierce, Evan Beth Taber, Jodi Schucker.   

Abstract

BACKGROUND: Rare cases of hemolytic disease of the newborn occur in women with genetic variants of the D antigen. A partial D variant might be suspected when typing for the D antigen shows weaker-than-normal reactions (weak D). Historically, patients with a weak D phenotype have not been considered candidates for Rh immune globulin prophylaxis. CASE: A gravida 2, para 1 woman with A-positive blood type, delivered an infant who died from severe hemolytic disease of the newborn 6 days after birth. Anti-D, undetectable at the first prenatal visit, was identified (titer 1:64) at delivery. The mother's red cells were partial D(VI) phenotype.
CONCLUSION: Although severe hemolytic disease in patients with partial D is rare, this neonatal death illustrates the need for a change in management of women with weak D.

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Year:  2003        PMID: 14607035     DOI: 10.1016/s0029-7844(03)00709-9

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  7 in total

Review 1.  Molecular genetics and clinical applications for RH.

Authors:  Willy A Flegel
Journal:  Transfus Apher Sci       Date:  2011-01-28       Impact factor: 1.764

Review 2.  Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype.

Authors:  S Gerald Sandler; Leonard N Chen; Willy A Flegel
Journal:  Br J Haematol       Date:  2017-05-16       Impact factor: 6.998

3.  It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. College of American Pathologists Transfusion Medicine Resource Committee Work Group.

Authors:  S Gerald Sandler; Willy A Flegel; Connie M Westhoff; Gregory A Denomme; Meghan Delaney; Margaret A Keller; Susan T Johnson; Louis Katz; John T Queenan; Ralph R Vassallo; Clayton D Simon
Journal:  Transfusion       Date:  2014-12-01       Impact factor: 3.157

4.  Strategies to identify candidates for D variant genotyping.

Authors:  Xunda Luo; Margaret A Keller; Ian James; Michelle Grant; Shiguang Liu; Kellie Simmons Massey; Andrew Czulewicz; Sandra Nance; Yanhua Li
Journal:  Blood Transfus       Date:  2017-04-05       Impact factor: 3.443

5.  Anti-D Antibodies in Pregnant D Variant Antigen Carriers Initially Typed as RhD.

Authors:  Jelena Lukacevic Krstic; Slavica Dajak; Jasna Bingulac-Popovic; Vesna Dogic; Jela Mratinovic-Mikulandra
Journal:  Transfus Med Hemother       Date:  2016-10-14       Impact factor: 3.747

6.  Anti-D reagents should be chosen accordingly to the prevalence of D variants in the obstetric population.

Authors:  Jelena Lukacevic Krstic; Slavica Dajak; Jasna Bingulac-Popovic; Vesna Dogic; Jela Mratinovic-Mikulandra
Journal:  J Clin Lab Anal       Date:  2017-06-26       Impact factor: 2.352

7.  RHD del28Phe (DMW) encoded by a novel in-frame deletion resulting in reduced D antigen expression.

Authors:  Eva Maria Matzhold; Helene Polin; Günther F Körmöczi; Susanne Macher; Marlies Schönbacher; Thomas Wagner
Journal:  Transfusion       Date:  2019-07-23       Impact factor: 3.157

  7 in total

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