Severe hemolytic disease of the fetus and newborn due to allo‐anti‐D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31)
Transfusion2018Vol. 58(10), pp. 2260–2264
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Elona Turley, Eunike C. McGowan, Catherine A. Hyland, Elizna M. Schoeman, Robert L. Flower, Amanda Skoll, Marie‐France Delisle, Tanya N. Nelson, Gwen Clarke, Nicholas Au
Abstract
The RHD allele, RHD*148+1T, results in a partial Del phenotype, and the anti-D formed in pregnant women with this phenotype is capable of causing severe HDFN.
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