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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Bibliographic Details
Published in:Wellcome Open Res
Main Authors: 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
Format: Artigo
Language:Inglês
Published: F1000 Research Limited 2018
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5829521/
https://ncbi.nlm.nih.gov/pubmed/29552643
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/wellcomeopenres.13373.1
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