Literature DB >> 24020803

New RHCE variant alleles encoding the D- - phenotype.

Gorka Ochoa-Garay1, Joann M Moulds, Jacqueline Cote, Lesley Kresie, Adirane Garaizar, Mindy Goldman, Polly Wynn.   

Abstract

BACKGROUND: Variant alleles that do not produce RhCE antigens are rare. Consequently, they pose a challenge to transfusion when found in alloimmunized patients and make blood units valuable when found in donors. STUDY DESIGN AND METHODS: Five index cases and their relatives were studied by both serologic and molecular techniques. Genomic DNA was subjected to microarray genotyping, sequencing, exon scanning, and/or copy number determination assays to identify the RHCE allele(s) responsible for their D+ C- c- E- e- (D- -) phenotype.
RESULTS: The five apparent D- - phenotypes were confirmed by molecular methods. Three of them contained unreported RHCE-null alleles, namely, RHCE*Ce-D(3-9)-Ce, RHCE*Ce87_93insT, and RHCE*cE221A.
CONCLUSION: Molecular analysis of D- - phenotypes allows the identification of new RHCE-null variants. Conversely, detection of described RHCE-null variants facilitates confirmation of D- - phenotypes in patients and donors, helping improve transfusion safety. Published 2013. This article is a U.S. Government work and is in the public domain in the USA.

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Year:  2013        PMID: 24020803     DOI: 10.1111/trf.12404

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  2 in total

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2.  Molecular characterization of rare D--/D-- variants in individuals of Indian origin.

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Journal:  Blood Transfus       Date:  2020-11-27       Impact factor: 3.443

  2 in total

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