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D−− phenotype caused by a novel RHCE null allele.

Authors :
Principi, Cintia
Trucco Boggione, Carolina
Ensinck, Alejandra
Posner, Victoria
Luján Brajovich, Melina
Stettler, Silvina
Mattaloni, Stella
Biondi, Claudia
Cotorruelo, Carlos
Source :
Transfusion; Feb2024, Vol. 64 Issue 2, pE3-E5, 3p
Publication Year :
2024

Abstract

This article discusses a rare blood phenotype known as D−−, which is characterized by the absence of RhCE antigens on red blood cells (RBCs) and often accompanied by increased D antigen expression. The study analyzes a blood sample from an Argentinean patient with the D−− phenotype and investigates the serologic and molecular aspects of the condition. The results reveal a new hybrid RHCE null allele, designated as RHCE*01N.16, which is responsible for the D−− phenotype and exhibits enhanced D antigen expression. This finding is considered unusual in all populations. The study was supported by grants from the Agencia Nacional de Promoción Científica y Tecnológica and Universidad Nacional de Rosario in Argentina. [Extracted from the article]

Details

Language :
English
ISSN :
00411132
Volume :
64
Issue :
2
Database :
Complementary Index
Journal :
Transfusion
Publication Type :
Academic Journal
Accession number :
175567361
Full Text :
https://doi.org/10.1111/trf.17698