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HEMOGLOBINURIA FOLLOWING BLOOD TRANSFUSION IN SICKLE CELL HOMOZYGOUS PATIENT: DELAYED TRANSFUSION REACTION; A CASE REPORT
Journal: Indian Journal of Medical Research and Pharmaceutical Sciences (Vol.6, No. 10)Publication Date: 2019-10-30
Authors : Satyajit Parhi; Namita Mohanty;
Page : 14-15
Keywords : hemoglobinuria; sickle cell anemia; direct coombs test; transfusion reaction.;
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Abstract
The sickle hemoglobinopathies are hereditary disorders in which red cells contain Hb-S. Hb S ( a2b2 6 Glu-Val) polymerizes reversibly. Alloimmunization with sickle cell disease (SCD) has A very low incidence report.
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Last modified: 2019-10-24 07:21:06