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Glucose-6-Phosphate Dehydrogenase Status and Risk of Hemolysis in Plasmodium falciparum-Infected African Children Receiving Single-Dose Primaquine
Author(s) -
Chi Eziefula,
Helmi Pett,
Lynn Grignard,
Salome Opus,
Moses Ν. Kiggundu,
Moses R. Kamya,
Shunmay Yeung,
Sarah G. Staedke,
Teun Bousema,
Chris Drakeley
Publication year - 2014
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.02889-14
Subject(s) - primaquine , glucose 6 phosphate dehydrogenase , hemolysis , glucose 6 phosphate dehydrogenase deficiency , malaria , plasmodium falciparum , hemolytic anemia , glucosephosphate dehydrogenase deficiency , heterozygote advantage , dehydrogenase , biology , hemoglobin , hemoglobinopathy , enzyme , immunology , medicine , genotype , biochemistry , gene , chloroquine
Glucose-6-phosphate dehydrogenase (G6PD) enzyme function and genotype were determined in Ugandan children with uncomplicated falciparum malaria enrolled in a primaquine trial after exclusion of severe G6PD deficiency by fluorescent spot test. G6PD A- heterozygotes and hemizygotes/homozygotes experienced dose-dependent lower hemoglobin concentrations after treatment. No severe anemia was observed.

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