Glucose-6-phosphate dehydrogenase deficiency laboratory findings: Difference between revisions
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*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<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> | ||
* | *Elevated Lactate dehydrogenase in hemolysis | ||
*Decreased haptoglobin in hemolysis | |||
*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 | OR |
Revision as of 20:12, 14 August 2018
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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 [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
There are no diagnostic laboratory findings associated with [disease name].
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
- Neonatal hyperbilirubinemia[1]
- Elevated Lactate dehydrogenase in hemolysis
- Decreased haptoglobin in hemolysis
- 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
- ↑ 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.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.D. [3]