نتایج جستجو برای: glucose 6 phospate dehydrogenase deficiency
تعداد نتایج: 1271709 فیلتر نتایج به سال:
A deficiency in human erythrocyte glucose 6-phosphate dehydrogenase may be genetically determined (l-4) or occur in normal erythrocytes as they age in tivo (5, 6). The inherited glucose-6-P dehydrogenase deficiency, which is associated with hemolytic anemia upon exposure to a variety of agents, affords an opportunity in man to study further the mechanisms by which genes can lead to a decrease i...
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is common in tropical Sub-Saharan countries. The allele most frequently associated with G6PD deficiency in this a region is G6PD 376G/202A. Here, we show that, the prevalence of G6PD deficiency is 12% in the Sereer ethnic group from Senegal ant that the 376G/968C genotype is predominant; the frequency of the 376G/202A genotype is very low in t...
Glucose-6-phosphate dehydrogenase (G6PD) is the key enzyme that initiates pentose phosphate cycle in glucose metabolism. Physiologically, this pathway main source of nicotinamide adenine dinucleotide (NADPH) for red blood cells. This study aims to identify glucose-6-phosphate mutations Nung ethnic patients with G6PD deficiency. 18 pediatric group were diagnosed deficiency at Vietnam National Ch...
Abstract Background and objectives: Glucose-6-phosphate dehydrogenase (G6PD) is an enzyme in the pentose phosphate pathway. G6PD deficiency (an X-linked recessive hereditary disease) is an inherited condition affecting approximately 3% of the people globally. This deficiency can cause hemolytic anemia and jaundice in neonates. The goal of this study is to detect the prevalence of G6PD deficienc...
INTRODUCTION Glucose-6-phosphate dehydrogenase deficiency is an X-linked recessive disease that causes acute or chronic hemolytic anemia and potentially leads to severe jaundice in response to oxidative agents. This deficiency is the most common human innate error of metabolism, affecting more than 400 million people worldwide. CASE PRESENTATION Here, we present the first documented case of k...
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