نتایج جستجو برای: g6pd deficiency

تعداد نتایج: 137946  

2012
Qamar Ali Muhammad Aqeel Hamid Iqbal

Objective: To determine the frequency of Glucose 6 Phosphate Dehydrogenase (G6PD) deficiency in neonates presenting with jaundice. Material and Methods: This descriptive study was conducted at Special Care Baby Unit (SCBU) Department of Child Health, Khyber Teaching Hospital, Peshawar from January 2008 to June 2008. A total number of 283 newborns, aged 1-14 days of either sex admitted with jaun...

Journal: :Turkish Journal of Hematology 2010

Journal: :Genetics 2002
Matthew A Saunders Michael F Hammer Michael W Nachman

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy in humans. Deficiency alleles for this X-linked disorder are geographically correlated with historical patterns of malaria, and the most common deficiency allele in Africa (G6PD A-) has been shown to confer some resistance to malaria in both hemizygous males and heterozygous females. We studied DNA sequence varia...

2017
Hasan M. Isa Masooma S. Mohamed Afaf M. Mohamed Adel Abdulla Fuad Abdulla

PURPOSE This study aimed to determine the prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency among infants with neonatal indirect hyperbilirubinemia (NIH); compare G6PD-deficient and G6PD-normal patients regarding hyperbilirubinemia and need for exchange transfusions (ET); and assess risk factors for ET and kernicterus. METHODS This is a case-control retrospective study. Medica...

Journal: :Croatian medical journal 2006
Josko Markić Vjekoslav Krzelj Anita Markotić Eugenija Marusić Luka Stricević Jaksa Zanchi Nada Bosnjak Ada Sapunar

AIM To determine the prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in the population of the town of Komiza on the island of Vis, which has previously been reported as a place with several cases of favism. METHODS We screened 302 randomly selected men, using the fluorescent spot test. Fluorescence readings were performed at the beginning and 5, 10, and 20 minutes after incu...

2017
Nanae Takahashi Takashi Ogawa Zen’ichiro Wajima Akibumi Omi

RATIONALE Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, resulting in deficits in nicotinamide adenine dinucleotide phosphate production, an important intracellular antioxidant enzyme. G6PD-deficient subjects present with a susceptibility of erythrocytes to oxidative stress and hemolysis, and should avoid drugs or stressors that have oxidative action...

Journal: :Cukurova Medical Journal 2022

Purpose: The aim of this study was to investigate in vitro effect glyphosate on Glucose 6-phosphate dehydrogenase (G6PD) enzyme activity.
 Materials and Methods: In terms G6PD deficiency, samples taken from healthy deficient male individuals were studied. After the hemolysates prepared blood sample, enyzme activities determined by modified Beutler method. Then, effects different concentrat...

Journal: :The Southeast Asian journal of tropical medicine and public health 2003
George S T Chen Cristy L Peterson

Glucose-6-phosphate dehydrogenase (G6PD) is the initial enzyme in the hexose monophosphate pathway of glucose metabolism. Deficiency of G6PD has been linked to increased sensitivity of red cells to hemolytic anemia due to certain oxidant drugs, infectious agents or fava beans. It is an inherited error in metabolism and has a high incidence in certain ethnic groups. Astoria-Pacific has developed...

Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common disease of the hexose monophosphate pathway existing in more than 400 million people worldwide. The aim of this study was to identify neonates with G6PD deficiency following national program for screening and education of affected newborns’ parents started since June 2007 in Mazandaran, a northern Province of Ira...

2018
Bushra Moiz Sidra Asad Ali

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked disorder affecting some 400 million people worldwide. Though clinically silent, it may result in hemolysis on oxidative stress induced by drugs or infections. Viral hepatitis A with coexisting G6PD deficiency can be devastating associated with severe hemolysis, anemia, renal failure, and hepatic encephalopathy.

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