Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a prevalent condition worldwide and is caused by loss-of-function mutations in the G6PD gene. Individuals with deficiency are more susceptible to oxidative stress which leads to the classical, acute hemolytic anemia (favism). However, G6PD defic...

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Detalles Bibliográficos
Autores principales: Lee, Heng Yang, Ithnin, Azlin, Azma, Raja Zahratul, Othman, Ainoon, Salvador, Armindo, Cheah, Fook Choe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170901/
https://www.ncbi.nlm.nih.gov/pubmed/35685917
http://dx.doi.org/10.3389/fped.2022.875877

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170901/
https://www.ncbi.nlm.nih.gov/pubmed/35685917
http://dx.doi.org/10.3389/fped.2022.875877

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