Purpose of the Screen
- Detect inherited G6PD enzyme deficiency.
- Prevent sudden hemolytic anemia episodes.
- Identify unsafe medications and foods for the patient.
Book G6PD Deficiency Test in Saudi Arabia | Lahalak Medical Platform
Protect yourself and your family from sudden hemolytic crises by accurately measuring G6PD enzyme activity. This test helps you identify triggers, avoid high-risk medications and foods, and ensure long-term safety.
Scientific name: Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Screen
A laboratory test measuring G6PD enzyme levels in red blood cells to detect genetic deficiency. It prevents hemolytic anemia triggered by specific factors like fava beans or certain medications.
Service type
Laboratory test
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Blood sample collection
- Quantitative enzyme assay
- Results report
Medical Service Information
Target Groups
- Newborns as part of early screening.
- Individuals with a family history of the deficiency.
- Patients with unexplained anemia or jaundice.
When to Perform the Test
- To confirm genetic safety profile.
- Before starting medications like antimalarials.
- Following symptoms like sudden paleness or dark urine.
Conditions & Notices
- Testing should be avoided during an acute hemolytic episode
- Inform the lab about any medications being taken
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