HEMOCHROMATOSIS (C282Y, H63D) GENE MUTATION DETECTION, EDTA BLOOD

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The Hemochromatosis Gene Mutation test detects C282Y and H63D mutations in the HFE gene, which are linked to hereditary hemochromatosis—an iron overload disorder. Identifying these mutations helps evaluate genetic risk, guide early interventions, and prevent complications such as liver disease, diabetes, or heart problems. Metropolis Healthcare performs this test using advanced molecular techniques on EDTA blood samples to ensure accurate and reliable results. It is recommended for individuals with a family history of hemochromatosis, unexplained high iron levels, or related symptoms. The test supports personalized management and long-term monitoring 

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Price: Rs. 8,160.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: H0002

Frequently Asked Questions (FAQ's):

What does the Hemochromatosis Gene Mutation test detect at Metropolis Healthcare?
It identifies C282Y and H63D mutations in the HFE gene associated with hereditary hemochromatosis.

Why is this test important at Metropolis Healthcare?
It helps assess genetic risk for iron overload and enables early preventive interventions.

Who should take this test at Metropolis Healthcare?
Individuals with family history of hemochromatosis, unexplained high iron or ferritin levels, or related clinical symptoms.

How does Metropolis Healthcare perform this gene mutation test?
Using advanced PCR and sequencing-based molecular techniques for precise detection.

What sample type is required at Metropolis Healthcare?
A blood sample collected in an EDTA tube is required.

Is fasting required before testing at Metropolis Healthcare?
No fasting or special preparation is needed.

How long does it take to get results from Metropolis Healthcare?
Results are usually available within the standard molecular genetics turnaround time.

Can Metropolis Healthcare provide follow-up advice after mutation detection?
Yes, Metropolis Healthcare can guide genetic counseling, iron monitoring, and management strategies

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