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).
Elona TurleyEunike C McGowanCatherine A HylandElizna M SchoemanRobert L FlowerAmanda SkollMarie-France DelisleTanya NelsonGwen ClarkeNicholas AuPublished in: Transfusion (2018)
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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