Diagnostic performances of the fluorescent spot test for G6PD deficiency in newborns along the Thailand-Myanmar border: A cohort study

Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited enzymatic disorder associated with severe neonatal hyperbilirubinemia and acute haemolysis after exposure to certain drugs or infections. The disorder can be diagnosed phenotypically with a fluorescent spot test (FST), w...

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Detalles Bibliográficos
Autores principales: Thielemans, Laurence, Gornsawun, Gornpan, Hanboonkunupakarn, Borimas, Paw, Moo Kho, Porn, Pen, Moo, Paw Khu, Van Overmeire, Bart, Proux, Stephane, Nosten, François, McGready, Rose, Carrara, Verena I., Bancone, Germana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829521/
https://www.ncbi.nlm.nih.gov/pubmed/29552643
http://dx.doi.org/10.12688/wellcomeopenres.13373.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829521/
https://www.ncbi.nlm.nih.gov/pubmed/29552643
http://dx.doi.org/10.12688/wellcomeopenres.13373.1

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