Glucose-6-phosphate dehydrogenase deficiency laboratory findings: Difference between revisions

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==Overview==
==Overview==
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].


OR
Laboratory findings consistent with the diagnosis of G6PD deficiency include hemoglobinuria, neonatal hyperbilirubinemia, elevated Lactate dehydrogenase in hemolysis
 
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
 
OR
 
[Test] is usually normal for patients with [disease name].
 
OR
 
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
 
OR
 
There are no diagnostic laboratory findings associated with [disease name].


==Laboratory Findings==
==Laboratory Findings==


There are no diagnostic laboratory findings associated with [disease name].
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>
 
OR
 
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
 
OR
 
[Test] is usually normal among patients with [disease name].
 
OR
 
Laboratory findings consistent with the diagnosis of G6PD deficiency include:
*Hemoglobinuria
*Hemoglobinuria
*Neonatal hyperbilirubinemia<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>
*Neonatal hyperbilirubinemia
*Elevated Lactate dehydrogenase in hemolysis
*Elevated Lactate dehydrogenase in hemolysis
*Decreased haptoglobin in hemolysis
*Decreased haptoglobin in hemolysis
*Negative direct antiglobulin test or coombs test in non immumne hemolysis meidated by G6PD  
*Negative direct antiglobulin test or coombs test in non immumne hemolysis meidated by G6PD  
** Lactate dehydrogenase
** Lactate dehydrogenase (elevated in hemolysis and a marker of hemolytic severity)
** Haptoglobin (decreased in hemolysis);
** A "direct antiglobulin test" (Coombs' test) – this should be negative, as hemolysis in G6PD is not immune-mediated;
OR
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].


==References==
==References==

Revision as of 17:14, 5 September 2018


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Mahda Alihashemi M.D. [1]

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

  1. ↑ 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.

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.D. [3]

Overview

Laboratory diagnosis

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