Point-of-Care Testing for G6PD Deficiency: Opportunities for Screening

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, an X-linked genetic disorder, is associated with increased risk of jaundice and kernicterus at birth. G6PD deficiency can manifest later in life as severe hemolysis, when the individual is exposed to oxidative agents that range from foods such as...

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Detalles Bibliográficos
Autores principales: Anderle, Athena, Bancone, Germana, Domingo, Gonzalo J., Gerth-Guyette, Emily, Pal, Sampa, Satyagraha, Ari W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832607/
https://www.ncbi.nlm.nih.gov/pubmed/31709308
http://dx.doi.org/10.3390/ijns4040034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832607/
https://www.ncbi.nlm.nih.gov/pubmed/31709308
http://dx.doi.org/10.3390/ijns4040034

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