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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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| Publicado no: | Int J Neonatal Screen |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2018
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| Assuntos: | |
| Acesso em linha: | 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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