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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Bibliografische gegevens
Gepubliceerd in:Int J Neonatal Screen
Hoofdauteurs: Anderle, Athena, Bancone, Germana, Domingo, Gonzalo J., Gerth-Guyette, Emily, Pal, Sampa, Satyagraha, Ari W.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: MDPI 2018
Onderwerpen:
Review
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6832607/
https://ncbi.nlm.nih.gov/pubmed/31709308
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijns4040034
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