Results 31 to 40 of about 1,019,197 (220)

Correlation Between Glucose – 6 – Phosphate Dehydrogenase Deficiency Level and Some Haematological Parameters on Newborn Blood in Al-Anbar Governorate-Ramadi [PDF]

مجلة جامعة الانبار للعلوم الصرفة, 2012
This study aimed to determine the prevalence of Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Al-Anbar Governorate-Ramadi and to study the different relationships between these cases and different haematological parameters values. In addition to
Sabri M. Hussain, Mohammed Q.Al-Ani, Khalid F.Al-Rawi, Mahmood. M.Atia   +3 more
doaj   +1 more source

Combined effects of double mutations on catalytic activity and structural stability contribute to clinical manifestations of glucose-6-phosphate dehydrogenase deficiency

Scientific Reports, 2021
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy in humans, affecting ~ 500 million worldwide. A detailed study of the structural stability and catalytic activity of G6PD variants is required to understand how different ...
Phonchanan Pakparnich, Sirapapha Sudsumrit, Mallika Imwong, Teeraporn Suteewong, Kamonwan Chamchoy, Danaya Pakotiprapha, Ubolsree Leartsakulpanich, Usa Boonyuen   +7 more
doaj   +1 more source

Glucose-6-phosphate dehydrogenase deficiency in Nigerian children. [PDF]

PLoS ONE, 2013
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy and in Sub-Saharan Africa, is a significant cause of infection- and drug-induced hemolysis and neonatal jaundice.
Olatundun Williams, Daniel Gbadero, Grace Edowhorhu, Ann Brearley, Tina Slusher, Troy C Lund   +5 more
doaj   +1 more source

Molecular characterization of G6PD mutations identifies new mutations and a high frequency of intronic variants in Thai females.

PLoS ONE, 2023
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked enzymopathy caused by mutations in the G6PD gene. A medical concern associated with G6PD deficiency is acute hemolytic anemia induced by certain foods, drugs, and infections.
Kamonwan Chamchoy, Sirapapha Sudsumrit, Jutamas Wongwigkan, Songsak Petmitr, Duantida Songdej, Emily R Adams, Thomas Edwards, Ubolsree Leartsakulpanich, Usa Boonyuen   +8 more
doaj   +1 more source

G6PD DEFICIENCY

The Professional Medical Journal, 2015
Context: Hyperbilirubinemia due to glucose 6 phosphate dehydrogenase(G6PD) deficiency can cause permanent neurological damage and death in neonates.Screening for the enzyme enables timely diagnosis and treatment in cases of G6PD relatedkernicterus. Knowledge of patient G6PD status is also important in treatment of malaria, adisease endemic in Pakistan.
Zahra Rashid Khan, Shumaila Najeeb, Alina Amjad   +2 more
openaire   +2 more sources

The potential link between inherited G6PD deficiency, oxidative stress, and vitamin D deficiency and the racial inequities in mortality associated with COVID-19

Free Radical Biology & Medicine, 2020
There is a marked variation in mortality risk associated with COVID-19 infection in the general population. Low socioeconomic status and other social determinants have been discussed as possible causes for the higher burden in African American ...
S. Jain, R. Parsanathan, S. Levine, J. Bocchini, M. Holick, J. Vanchiere   +5 more
semanticscholar   +1 more source

Geographical Accessibility to Glucose-6-Phosphate Dioxygenase Deficiency Point-of-Care Testing for Antenatal Care in Ghana

Diagnostics, 2020
Background: Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency screening test is essential for malaria treatment, control, and elimination programs. G6PD deficient individuals are at high risk of severe hemolysis when given anti-malarial drugs such as ...
Desmond Kuupiel, Kwame M. Adu, Vitalis Bawontuo, Duncan A. Adogboba, Paul K. Drain, Mosa Moshabela, Tivani P. Mashamba-Thompson   +6 more
doaj   +1 more source

Prevalence of G6PD deficiency in Thai blood donors, the characteristics of G6PD deficient blood, and the efficacy of fluorescent spot test to screen for G6PD deficiency in a hospital blood bank setting

Hematology, 2022
Background Transfusion of blood from glucose-6-phosphate dehydrogenase (G6PD) enzyme deficient donors could cause a potentially unfavorable outcome, especially in newborns and those with hemoglobinopathies.
Phinyada Rojphoung, Thongbai Rungroung, Usanee Siriboonrit, Sasijit Vejbaesya, Parichart Permpikul, Janejira Kittivorapart   +5 more
doaj   +1 more source

To determine the prevalence of glucose-6-phosphate dehydrogenase deficiency using a novel water-soluble tetrazolium-8 formazan method' for neonatal screening in region of Himachal Pradesh, India

Advances in Human Biology, 2019
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most significant enzyme defect in India with an incidence ranging from 2% to 27.9% in different communities.
Seema Sharma, Milap Sharma
doaj   +1 more source

A literature review and case report of severe hepatitis caused by the G6PD gene c.1478G>A muta-tion [PDF]

Yixue xinzhi zazhi, 2021
G6PD (glucose-6-phosphate dehydrogenase) deficiency is the most common enzyme deficiency disease in humans affecting over 500 million people worldwide, with most patients being children aged 2 to 10 years.
Jian LIU, Yan-Jun WANG, Shun-Jun XIONG, Bing-Yan HE, You-Ping DENG, Dong-Chi ZHAO   +5 more
doaj   +1 more source