| Literature DB >> 21479984 |
Marie-Hélène Odièvre1,2,3, Névéna Danékova4, Bettina Mesples4, Myriam Chemouny5, Nathalie Couque6, Nathalie Parez4,5, Rolande Ducrocq6,7, Jacques Elion8,6,7.
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.Entities:
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Year: 2011 PMID: 21479984 DOI: 10.1007/s12185-011-0827-6
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490