G6PD GENE MUTATION DETECTION / EDTA BLOOD

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NABL Cap Accredited    
The G6PD Gene Mutation Detection test by Metropolis Healthcare identifies pathogenic variants in the G6PD gene that cause Glucose-6-Phosphate Dehydrogenase Deficiency, a common hereditary enzyme disorder. This condition can lead to hemolytic anemia triggered by infections, certain foods, or medications. Using advanced molecular techniques, the test accurately detects G6PD gene mutations from an EDTA blood sample. Metropolis Healthcare provides precise results to support diagnosis, risk assessment, and personalized clinical management

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Price: Rs. 4,620.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0073

Frequently Asked Questions (FAQ's):

What does this test detect?
It identifies mutations in the G6PD gene that lead to G6PD deficiency, a hereditary enzymatic disorder causing hemolysis.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses sensitive molecular methods to detect clinically significant variants within the G6PD gene.

Who should consider this test?
Individuals with unexplained jaundice, hemolytic anemia, neonatal jaundice, or a family history of G6PD deficiency.

What sample is required?
An EDTA whole blood sample is used for DNA extraction and mutation analysis.

Is any preparation needed before testing?
No fasting or special preparation is required for this genetic test.

How long do results take at Metropolis Healthcare?
Results are usually available within a few working days depending on laboratory workflow.

How will the results help?
They confirm diagnosis, guide avoidance of triggering substances, and support genetic counselling for affected families.

Can this test help identify carriers?
Yes, Metropolis Healthcare can identify carrier status, especially important for families with known G6PD mutations

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