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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Detaylı Bibliyografya
Yayımlandı:Int J Neonatal Screen
Asıl Yazarlar: Anderle, Athena, Bancone, Germana, Domingo, Gonzalo J., Gerth-Guyette, Emily, Pal, Sampa, Satyagraha, Ari W.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2018
Konular:
Review
Online Erişim: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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