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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Wellcome Open Res
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: F1000 Research Limited 2018
विषय:
Research Article
ऑनलाइन पहुंच: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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