G6PD-Quantitative

G6PD deficiency should be classified as hereditary diseases. People with the disease in the normal functioning of red blood cells, in the absence of the enzyme glucose 6-phosphate dehydrogenase is disrupted. People with this disease may occur after taking certain medications, foods or infected with some infections, are experiencing hemolytic anemia. Most patients are asymptomatic, but some patients when red blood cell destruction (hemolysis) will develop symptoms of anemia. Symptoms disappear after causing hemolysis, are destroyed. In a very small number of patients, G6PD deficiency leads to anemia becomes chronic. In these patients, the blood's ability to carry Akshyzhn to tissues and removing carbon dioxide does. Color plasma of patients due to the destruction of red blood cells and the release of hemoglobin inside them, pink or red. Babies with this condition may cause jaundice.