P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management

Conclusion:This report documents a rare case of the P-null phenotype with an alloanti-PP1Pk causing a severe HTR to transfusion of the trial dose of the least incompatible blood. The case is the first example of this specificA4GALTmutation found in India.Transfus Med Hemother

https://www.karger.com/Article/FullText/514499

Source: Transfusion Medicine and Hemotherapy - February 25, 2021 Category: Hematology Source Type: research