Secondary Reporting of G6PD Deficiency on Newborn Screening

In April 2019, the Alberta Newborn Screening Program expanded to include screening for classic galactosemia using a two-tier screening approach. This approach secondarily identifies infants with glucose-6-phosphate dehydrogenase (G6PD) deficiency. The goals of this study were (i) to evaluate the per...

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Detalles Bibliográficos
Autores principales: Hoang, Stephanie C., Blumenschein, Pamela, Lilley, Margaret, Olshaski, Larissa, Bruce, Aisha, Wright, Nicola A. M., Ridsdale, Ross, Christian, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123647/
https://www.ncbi.nlm.nih.gov/pubmed/37092512
http://dx.doi.org/10.3390/ijns9020018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123647/
https://www.ncbi.nlm.nih.gov/pubmed/37092512
http://dx.doi.org/10.3390/ijns9020018

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