Glucose-6-phosphate dehydrogenase deficiency
Other Names for this Disease
- G6PD deficiency
- Hemolytic anemia due to G6PD deficiency
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hemolysis) when the body is exposed to certain foods, drugs, infections or stress. This condition occurs when a person is missing or doesn't have enough glucose-6-phosphate dehydrogenase, an enzyme which helps red blood cells work properly. G6PD deficiency is more likely to occur in males, particularly African Americans, and those from certain parts of Africa, Asia, and the Mediterranean. This condition is inherited in an X-linked recessive manner and is caused by mutations in the G6PD gene. Treatment may involve medicines to treat an infection, stopping drugs that are causing red blood cell destruction, and/or transfusions, in some cases.Glucose 6 phosphate dehydrogenase (G6PD) deficiency is a hereditary condition in which red blood cells break down (
Last updated: 7/23/2015
- Todd Gersten. Glucose-6-phosphate deficiency. MedlinePlus. February 24, 2014; http://www.nlm.nih.gov/medlineplus/ency/article/000528.htm.
- Glucose-6-phosphate dehydrogenase deficiency. Genetics Home Reference (GHR). May 2006; http://www.ghr.nlm.nih.gov/condition/glucose-6-phosphate-dehydrogenase-deficiency. Accessed 10/11/2011.
- Genetics Home Reference (GHR) contains information on Glucose-6-phosphate dehydrogenase deficiency. This website is maintained by the National Library of Medicine.
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