Glucose-6-phosphate dehydrogenase deficiency screening
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Glucose-6-phosphate dehydrogenase deficiency Microchapters |
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Differentiating Glucose-6-phosphate dehydrogenase deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Glucose-6-phosphate dehydrogenase deficiency screening On the Web |
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American Roentgen Ray Society Images of Glucose-6-phosphate dehydrogenase deficiency screening |
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FDA on Glucose-6-phosphate dehydrogenase deficiency screening |
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CDC on Glucose-6-phosphate dehydrogenase deficiency screening |
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Glucose-6-phosphate dehydrogenase deficiency screening in the news |
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Directions to Hospitals Treating Glucose-6-phosphate dehydrogenase deficiency |
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Risk calculators and risk factors for Glucose-6-phosphate dehydrogenase deficiency screening |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.D. [2]
Overview
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive hereditary disease featuring abnormally low levels of the G6PD enzyme, which plays an important role in red blood cell function. Individuals with the disease may exhibit non-immune hemolytic anemia in response to a number of causes. It is closely linked to favism, a disorder characterized by a hemolytic reaction to consumption of broad beans, with a name derived from the Italian name of the broad bean (fava). Sometimes the name, favism, is alternatively used to refer to the enzyme deficiency as a whole.