نتایج جستجو برای: g6pd deficiency

تعداد نتایج: 137946  

اسدالهی, خیراله, دلیری, سلمان, رحیمی, نازیلا, سایه‌میری, کورش,

Background: The deficiency of enzyme glucose-6-phosphate dehydrogenase (G6PD) is among the most common genetic diseases in human. The deficiency of G6PD enzyme is one of the most common encountered enzymes, affecting about 400 million people and causing a wide range of undesirable clinical complications worldwide. The performed studies have reported a variety of statements about the relationshi...

Journal: :فیض 0
یوسف مرتضوی yousef mortazavi department of pathology, zanjan university of medical scinces, zanjan, iranزنجان، دانشگاه علوم پزشکی زنجان، گروه آسیب شناسی عبدالرضا اسماعیل زاده abdoreza esmaeilzadeh صدرالدین کلانتری sadroddein kalantari

background: glucose-6-phosphate dehydrogenase (g6pd) is an x-linked enzymopathy affecting about 400 million people worldwide. neonatal jaundice, drug induced haemolysis and infection-induced haemolysis may happen in some deficient individuals and lead to considerable mortality. the distribution of g6pd deficiency and the molecular genetics of this enzyme vary widely among different ethnic group...

Journal: :journal of sciences, islamic republic of iran 2009
m.r. noori-daloii

glucose-6-phosphate dehydrogenase (g6pd) in humans is in x-linked disorder, housekeeping enzyme and vital for the survival of every cell. it catalyses the oxidation of glucose-6-phosphate to 6-phospho gluconat in the first committed step of the pentose phosphate pathway, which provides cells with pentoses and reducing power in the form of nadph. nadph is required to protect the cells against ox...

Journal: :The Southeast Asian journal of tropical medicine and public health 2003
O Ainoon A Alawiyah Y H Yu S K Cheong N H Hamidah N Y Boo M Zaleha

Neonatal screening for G6PD deficiency has long been established in many countries. The aim of the study was to determine whether the routine semiquantitative fluorescent spot test could detect all cases of G6PD deficiency, including those cases with partial deficiency (residual red cell G6PD activity between 20-60% of normal). We compared the results of G6PD screening by the semiquantitative f...

Journal: :iranian journal of blood and cancer 0
adel baghersalimi bahram darbandi hamid alizadeh

platelet adherence surrounding leucocytes in a rosette formation or platelet satellitism is a rare phenomenon. this finding has been observed almost exclusively in ethylenediaminetetraacetic acid treated blood at room temperature. the mechanism underlying this phenomenon is not fully understood. in many reports of platelet satellitism platelets clump to polymorphonuclear neutrophils in healthy ...

2006
Cinzia Balestrieri Giancarlo Serra Cristiana Cauli Luchino Chessa Angelo Balestrieri

is known about the safety of RBV treatment in patients with concomitant glucose-6-phosphate dehydrogenase (G6PD) deficiency, who are inherently prone to hemolysis.5 We prospectively studied changes in hemoglobin (Hb) levels in 112 patients with chronic hepatitis C, associated or not with G6PD deficiency, during and after combination therapy. G6PD activity was tested by a spectrophotometric meth...

Journal: :American journal of physiology. Heart and circulatory physiology 2013
Peter A Hecker Jane A Leopold Sachin A Gupte Fabio A Recchia William C Stanley

Glucose-6-phosphate dehydrogenase (G6PD) catalyzes the rate-determining step in the pentose phosphate pathway and produces NADPH to fuel glutathione recycling. G6PD deficiency is the most common enzyme deficiency in humans and affects over 400 million people worldwide; however, its impact on cardiovascular disease is poorly understood. The glutathione pathway is paramount to antioxidant defense...

Journal: :مجله دانشگاه علوم پزشکی شهرکرد 0
سید محمد کاظم نوربخش seyed mohammad kazem norbahksh pediatric dept,shahrekord university of medical sciences,shahrekord,iranگروه اطفال، دانشگاه علوم پزشکی شهرکرد، شهرکرد، ایران کرمعلی کثیری kkaram-ali kasiri shahrekord,iranگروه اطفال، دانشگاه علوم پزشکی شهرکرد، شهرکرد، ایران اسدالله جلیل asadollah jalil general physician,shahrekord university of medical sciences,shahrekord,iranپزشک عمومی، دانشگاه علوم پزشکی شهرکرد، شهرکرد، ایران مرتضی هاشم زاده morteza hashem zade cellular and molecular research center,shahrekord university of medical sciences,shahrekord,iranمرکز تحقیقات سلولی و مولکولی، دانشگاه علوم پزشکی شهرکرد، شهرکرد، ایران

background and aims: glucose-6-phosphate dehydrogenase (g6pd) is the first enzyme in the route of pentose phosphate metabolism. this route fulfills an effective role in removing oxidant metabolites. deficiency of this enzyme causes decline in energy regeneration of red blood cells and hemolysis. in this study, application of fluorescence staining method in diagnosing the frequency of g6pd defic...

صداقت کابلی, محمدرضا, حقیقی, لادن, فیروزرای, محسن,

  Jaundice as a clinical symptom of hyperbillirubinemia will appear generally when the billirubin level is more than 7mg/dl. This temporary elevation of billirubin is caused by hemolysis of erythrocytes. Among several causes of pathologic hyperbillirubinemia in newborns X-linked G6PD deficiency may be the most important. Iran in one of the high risk countries. Due to the risk of death and sever...

Journal: :Journal of clinical pathology 1968
H C Lai M P Lai K S Leung

In a Chinese population 1,000 full-term male neonates and a further 117 jaundiced neonates of both sexes were studied in an investigation of the frequency of deficiency of erythrocyte glucose-6-phosphate dehydrogenase (G6PD). This enzyme was found to be deficient in 3.6% of male neonates. Correlation of the results with the birthplace of the 602 mothers who were known to come from Kwangtung pro...

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