Glucose 6-phosphate Dehydrogenase (G6PD), Erythrocytes


Reference Range

G6PD-deficiency is the most common erythrocyte enzyme deficiency. The G6PD gene is located on the X chromosome but the majority of hemizygous males are asymptomatic most of the time. However, a range of different clinical manifestations can be induced by a toxic or infectious insult. Acute hemolytic anemia can be induced by certain drugs or by the ingestion of a toxin. Fava beans, in particular are toxic for G6PD-deficient subjects, inducing severe hemolytic anemia (this predisposition is called favism). Similarly, certain infections (including infectious mononucleosis and viral hepatitis) can induce hemolytic anemia in such subjects. Heterozygous females are usually completely asymptomatic.

Special Requirements

Minimum 1mL EDTA whole blood. Determine RBC count or Haemoglobin concentration prior to assay

Ready within 1

Copyright © biolab 2024, Developed by Tech Factory

Hit enter to search or ESC to close