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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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Dettagli Bibliografici
Pubblicato in:Int J Neonatal Screen
Autori principali: Anderle, Athena, Bancone, Germana, Domingo, Gonzalo J., Gerth-Guyette, Emily, Pal, Sampa, Satyagraha, Ari W.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2018
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Accesso online: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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