Molecular epidemiological investigation of G6PD deficiency in Yangjiang region, western Guangdong province [PDF]
Frontiers in Genetics, 2023 Objectives: The prevalence of G6PD deficiency has not been reported in Yangjiang, a western city in Guangdong province. This study aims to investigate the molecular characteristics of G6PD deficiency in this region.Methods: Blood samples were collected ...
Hong-Feng Liang +14 more
doaj +2 more sources
Newborn screening for G6PD deficiency in HeFei, FuYang and AnQing, China: Prevalence, cut-off value, variant spectrum [PDF]
Journal of Medical Biochemistry, 2023 Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive Mendelian genetic disorder characterized by neonatal jaundice and hemolytic anemia, affecting more than 400 million people worldwide.
Li Hui +8 more
doaj +3 more sources
Genotypic and phenotypic characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangzhou, China [PDF]
Human Genomics, 2023 Background G6PD deficiency is a common inherited disorder worldwide and has a higher incidence rate in southern China. Many variants of G6PD result from point mutations in the G6PD gene, leading to decreased enzyme activity.
Ziyan Li +9 more
doaj +2 more sources
Secondary Reporting of G6PD Deficiency on Newborn Screening [PDF]
International Journal of Neonatal Screening, 2023 In April 2019, the Alberta Newborn Screening Program expanded to include screening for classic galactosemia using a two-tier screening approach. This approach secondarily identifies infants with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Stephanie C. Hoang +7 more
doaj +2 more sources
Etiology analysis and G6PD deficiency for term infants with jaundice in Yangjiang of western Guangdong [PDF]
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 +2 more sources
Serum microRNAs as new biomarkers for detecting subclinical hemolysis in the nonacute phase of G6PD deficiency [PDF]
Scientific ReportsGlucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common enzymopathies worldwide. Patients with G6PD deficiency are usually asymptomatic throughout their life but can develop acute hemolysis after exposure to free radicals or certain
Kanyarat Boonpeng +5 more
doaj +2 more sources
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 +2 more sources
Scrub Typhus Infection Precipitating Hemolysis in a Patient With G6PD Deficiency: A Case Report [PDF]
Clinical Case ReportsGlucose‐6‐phosphate dehydrogenase (G6PD) deficiency is a well‐known red blood cell enzymopathy and a cause of intravascular hemolysis. This case report presents a child with underlying G6PD deficiency who experienced an acute episode of extensive ...
Ravi Shukla +5 more
doaj +2 more sources
Oseltamivir and G6PD deficiency
Turkish Journal of Hematology, 2010 Sinasi Ozsoylu
openaire +5 more sources
The association between glucose 6-phosphate dehydrogenase (G6PD) deficiency and attention deficit/hyperactivity disorder (ADHD) [PDF]
Eur PsychiatryKrone B.
europepmc +4 more sources