Glucose-6-phosphate dehydrogenase deficiency laboratory findings: Difference between revisions
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{{Glucose-6-phosphate dehydrogenase deficiency}} | {{Glucose-6-phosphate dehydrogenase deficiency}} | ||
{{MA}} | {{CMG}} {{shyam}}; {{AE}}{{MA}} [mailto:malihash@bidmc.harvard.edu] | ||
==Overview== | ==Overview== | ||
Laboratory findings consistent with the diagnosis of | Laboratory findings consistent with the diagnosis of G6PD deficiency include hemoglobinuria, neonatal hyperbilirubinemia, elevated lactate dehydrogenase in hemolysis. | ||
==Laboratory Findings== | ==Laboratory Findings== | ||
Laboratory findings consistent with the diagnosis of G6PD deficiency include:<ref name="pmid28461823">{{cite journal |vauthors=Isa HM, Mohamed MS, Mohamed AM, Abdulla A, Abdulla F |title=Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency |journal=Korean J Pediatr |volume=60 |issue=4 |pages=106–111 |date=April 2017 |pmid=28461823 |pmc=5410616 |doi=10.3345/kjp.2017.60.4.106 |url=}}</ref> | Laboratory findings consistent with the diagnosis of G6PD deficiency include:<ref name="pmid28461823">{{cite journal |vauthors=Isa HM, Mohamed MS, Mohamed AM, Abdulla A, Abdulla F |title=Neonatal indirect hyperbilirubinemia and glucose-6-phosphate dehydrogenase deficiency |journal=Korean J Pediatr |volume=60 |issue=4 |pages=106–111 |date=April 2017 |pmid=28461823 |pmc=5410616 |doi=10.3345/kjp.2017.60.4.106 |url=}}</ref> | ||
*Hemoglobinuria | *[[Hemoglobinuria]] | ||
*Neonatal hyperbilirubinemia | *Neonatal [[hyperbilirubinemia]] | ||
*Elevated | *Elevated lactate dehydrogenase in [[hemolysis]] | ||
*Decreased haptoglobin in hemolysis | *Decreased [[haptoglobin]] in [[hemolysis]] | ||
*Negative direct antiglobulin test or coombs test in non immumne hemolysis | *Negative direct antiglobulin test or [[coombs test]] in non immumne hemolysis | ||
==References== | ==References== | ||
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{{WS}} | {{WS}} | ||
[[Category: (name of the system)]] | [[Category: (name of the system)]] | ||
Latest revision as of 23:26, 19 December 2018
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Glucose-6-phosphate dehydrogenase deficiency Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]; Associate Editor(s)-in-Chief: Mahda Alihashemi M.D. [3] [4]
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
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.