Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a X-chromosomally transmitted disorder of the erythrocyte that affects 400 million people worldwide, occurring with increased frequency throughout Africa, Asia, the Mediterranean, and the Middle East. Prevalence of this deficiency has been found to be the gene mutations that affecting encoding of G6PD, which is correlated with the increased risk of neonatal jaundice,neonatal hyperbilirubinemia and drug or food-induced hem-olytic anemia.
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