Purpose of the Screening
- To diagnose the cause of persistent hemolytic anemia.
- To check enzyme levels before starting specific medications.
- To prevent sudden hemolytic crises triggered by fava beans or legumes.
Book G6PD Deficiency Test in Saudi Arabia | Lahalak Medical Platform
This screening identifies G6PD enzyme deficiency, commonly known as Favism. Early detection helps you avoid dietary and medicinal triggers that cause red blood cell breakdown, ensuring a safer and healthier lifestyle.
Scientific name: Glucose-6-Phosphate Dehydrogenase (G6PD) Activity Test
A quantitative lab test measuring G6PD enzyme activity in red blood cells. It diagnoses hereditary hemolytic anemia and helps patients avoid acute hemolytic crises triggered by specific foods, infections, or medications.
Service type
Laboratory test
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Venous blood sample
- Quantitative enzyme assay
- Result report
Medical Service Information
Target Groups
- Newborns for early screening and management.
- Individuals with unexplained jaundice or pale skin.
- Those with a family history of G6PD deficiency.
Symptoms Requiring the Test
- Sudden paleness or yellowish skin.
- Dark-colored urine (tea-colored).
- Rapid heart rate and shortness of breath.
Conditions & Notices
- Preferably performed outside acute hemolytic episodes
- Inform the doctor about current medications
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