Glucose-6-phosphate dehydrogenase deficiency laboratory findings: Difference between revisions
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{{Glucose-6-phosphate dehydrogenase deficiency}} | {{Glucose-6-phosphate dehydrogenase deficiency}} | ||
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==Overview== | ==Overview== | ||
Revision as of 17:17, 5 September 2018
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Glucose-6-phosphate dehydrogenase deficiency Microchapters |
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Differentiating Glucose-6-phosphate dehydrogenase deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mahda Alihashemi M.D. [2]
Overview
Laboratory findings consistent with the diagnosis of G6PD deficiency include hemoglobinuria, neonatal hyperbilirubinemia, elevated Lactate dehydrogenase in hemolysis
Laboratory Findings
Laboratory findings consistent with the diagnosis of G6PD deficiency include:[1]
- Hemoglobinuria
- Neonatal hyperbilirubinemia
- Elevated Lactate dehydrogenase in hemolysis
- Decreased haptoglobin in hemolysis
- Negative direct antiglobulin test or coombs test in non immumne hemolysis meidated by G6PD
References
- ↑ Isa HM, Mohamed MS, Mohamed AM, Abdulla A, Abdulla F (April 2017). "Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency". Korean J Pediatr. 60 (4): 106–111. doi:10.3345/kjp.2017.60.4.106. PMC 5410616. PMID 28461823.