Results 31 to 40 of about 22,836 (233)
Frontiers in Pediatrics, 2023 ObjectiveGlucose 6-phosphate dehydrogenase (G6PD) deficiency increases the risk of neonatal hyperbilirubinemia. The aim of this study is to evaluate the risk factors associated with hyperbilirubinemia in infants from the western part of Guangdong ...
Yi-Kang Yang +16 more
doaj +1 more source
Impact of the method of G6PD deficiency assessment on genetic association studies of malaria susceptibility. [PDF]
PLoS ONE, 2009 BACKGROUND:Clinical association studies have yielded varied results regarding the impact of glucose-6-phosphate dehydrogenase (G6PD) deficiency upon susceptibility to malaria.
Marla K Johnson +4 more
doaj +1 more source
Deficiência de glicose-6-fosfato desidrogenase eritrocitária em recém-nascidos do sexo masculino e sua relação com a icterícia neonatal [PDF]
, 2010 Glucose-6-phosphate dehydrogenase (G6PD) deficiency, the commonest red cell enzymopathy in humans, has an X-linked inheritance. The major clinical manifestations are drug induced hemolytic anemia, neonatal jaundice and chronic nonspherocytic hemolytic ...
AMORIM, Maria do Socorro T. +6 more
core +1 more source
G6PD diaxBox: Digital image-based quantification of G6PD deficiency
Talanta, 2021 Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy in humans. More than 400 million people worldwide are affected by this genetic condition. Testing for G6PD deficiency before drug administration is essential for patient safety. Rapidly ascertaining the G6PD status of a person is desirable for proper treatment.
Duangdao Palasuwan +5 more
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Glucose-6-phosphate dehydrogenase (G6PD) Deficiency [PDF]
Iranian Journal of Public Health, 2008 Glucose-6-phosphate dehydrogenase (G6PD) Deficiency is the most prevalent enzymopathy in mankind. It has sex-linked inheritance. This enzyme exists in all cells. G6PD deficiency increases the sensitivity of red blood cells to oxidative damage.
DD Farhud , L Yazdanpanah
doaj +1 more source
Qatar Medical Journal, 2004 G6PD deficiency is the most common enzyme deficiency disease worldwide, affecting 10% of the world's population. It is an X linked recessive disease therefore it affects males more than females (females are usually carriers of the disease).
A. Al Muzrakchi, A. A. Gehani
openaire +1 more source
Heliyon, 2023 Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder caused by a structural abnormality in the enzyme. G6PD deficiency is most prevalent among African, Asian, and Mediterranean people.
Woldeteklehaymanot Kassahun +3 more
doaj +1 more source
Plasmodium falciparum clearance with artemisinin-based combination therapy (ACT) in patients with glucose-6-phosphate dehydrogenase deficiency in Mali [PDF]
, 2010 URL : http://www.malariajournal.com/content/9/1/332Background: Artemisinin-based combination therapy (ACT) is currently the most effective medicine for the treatment of uncomplicated malaria.
Abdoulaye K Kone +9 more
core +2 more sources
Incidence and mutation analysis of glucose-6-phosphate dehydrogenase deficiency in eastern indonesian populations [PDF]
, 2010 We conducted a field survey of glucose-6-phosphate dehydrogenese (G6PD) deficiency in the eastern Indonesian islands, and analyzed G6PD variants molecularly. The incidence of G6PD deficiency in 5 ethnic groups (Manggarai, Bajawa, Nage-Keo, Larantuka, and
Dachlan, Yoes P. +8 more
core +1 more source
Liver Failure in Neonates With G6PD Deficiency
ACG Case Reports Journal, 2022 ABSTRACT Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a commonly inherited enzyme defect that can present with hemolysis, hyperbilirubinemia, and jaundice and may cause kidney and liver dysfunction. G6PD deficiency may serve as a cofactor for chronic liver disease; however, an association with liver failure is not well described. We
Milaan Shah, Vani Gopalareddy
openaire +2 more sources