Abstract
We report the occurrence of symptomatic methemoglobinemia in a previously healthy boy, who presented with severe acute hemolysis after fava bean ingestion. The methemoglobinemia revealed a previously unrecognized glucose-6-phosphate dehydrogenase (G6PD) deficiency. We discuss the pathophysiology of severe methemoglobinemia when associated with acute hemolysis, favism, and the common African G6PD A-variant [G6PD, VAL68MET, ASN126ASP]. In conclusion, screening for G6PD deficiency must be considered in symptomatic methemoglobinemia, especially in young boys, when associated with intravascular hemolysis.
MeSH terms
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Algeria
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Child
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Eating
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Favism / complications
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Favism / diagnosis*
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Favism / physiopathology
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Glucosephosphate Dehydrogenase / blood*
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Glucosephosphate Dehydrogenase / genetics
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Glucosephosphate Dehydrogenase Deficiency / complications
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Glucosephosphate Dehydrogenase Deficiency / diagnosis*
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Glucosephosphate Dehydrogenase Deficiency / physiopathology
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Hemolysis / drug effects
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Hemolytic Agents / administration & dosage
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Hemolytic Agents / adverse effects
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Humans
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Male
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Methemoglobinemia / complications
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Methemoglobinemia / diagnosis*
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Methemoglobinemia / physiopathology
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Mutation
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Vicia faba / adverse effects
Substances
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Hemolytic Agents
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Glucosephosphate Dehydrogenase