ENZIM G6PD PDF

Glucosephosphate dehydrogenase deficiency is a genetic disorder that occurs almost exclusively in males. This condition mainly affects red blood cells, which carry oxygen from the lungs to tissues throughout the body. In affected individuals, a defect in an enzyme called glucosephosphate dehydrogenase causes red blood cells to break down prematurely. This destruction of red blood cells is called hemolysis.

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Untuk maklumat lanjut, sila hubungi Layari : www. Hemolytic Anaemia damage of the red blood G6PD deficiency is inherited and usually cells , which can cause: occurs in males.

Shortness of breath 5. Chronic jaundice Sulphonamides G6PD screening is done in all hospitals 6. Enlarged spleen Co-trimoxazole and maternal clinics for newborns by Dapsone taking blood specimens from their Chloramphenicol. Aspirin Those with G6PD deficiency will have Always check with your doctor or Phenacetin damaged or destruction of the red blood pharmacist before taking any Sulphasalazine cells when they are exposed to infection, medications.

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Penyakit Kekurangan Enzim G6PD

Untuk maklumat lanjut, sila hubungi Layari : www. Hemolytic Anaemia damage of the red blood G6PD deficiency is inherited and usually cells , which can cause: occurs in males. Shortness of breath 5. Chronic jaundice Sulphonamides G6PD screening is done in all hospitals 6. Enlarged spleen Co-trimoxazole and maternal clinics for newborns by Dapsone taking blood specimens from their Chloramphenicol.

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Glucose-6-phosphate dehydrogenase

This enzyme participates in the pentose phosphate pathway see image , a metabolic pathway that supplies reducing energy to cells such as erythrocytes by maintaining the level of the co-enzyme nicotinamide adenine dinucleotide phosphate NADPH. The NADPH in turn maintains the level of glutathione in these cells that helps protect the red blood cells against oxidative damage from compounds like hydrogen peroxide. Clinically, an X-linked genetic deficiency of G6PD predisposes a person to non-immune hemolytic anemia. G6PD is widely distributed in many species from bacteria to humans. Other species experience a variation in G6PD as well.

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