Hemochromatosis Detection HFE Genotyping Test
Introduction
The Hemochromatosis Detection HFE Genotyping Test is a vital diagnostic tool designed to identify genetic mutations associated with hereditary hemochromatosis. This condition leads to excessive iron accumulation in the body, which can cause serious health issues, including liver disease, diabetes, and heart problems. Early detection through genetic testing can facilitate timely intervention, significantly improving patient outcomes.
What the Test Measures
This test detects specific genetic mutations in the HFE gene, including:
- H63D
- S65D
- C282Y
These mutations are linked to the risk of developing hemochromatosis and related complications.
Who Should Consider This Test
Individuals who may benefit from this test include:
- Those with a family history of hemochromatosis or iron overload disorders.
- Individuals experiencing symptoms such as fatigue, joint pain, abdominal pain, or skin discoloration.
- Patients with elevated serum ferritin or transferrin saturation levels.
Benefits of Taking the Test
Understanding your genetic risk through the Hemochromatosis Detection HFE Genotyping Test offers several benefits:
- Early identification of genetic predisposition to hemochromatosis.
- Guidance for lifestyle and dietary changes to manage iron levels.
- Informed decision-making regarding family planning and health monitoring.
- Potential to prevent serious health complications associated with iron overload.
Understanding Your Results
After taking the test, results will indicate whether you carry any of the identified mutations. A positive result may suggest a higher risk for developing hemochromatosis, while a negative result can provide peace of mind. Your healthcare provider will guide you through the interpretation of your results and recommend appropriate follow-up actions.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 140,000 NGN | 200,000 NGN |
Booking the Test
To book the Hemochromatosis Detection HFE Genotyping Test, please contact us at +2348110567037 via call or WhatsApp. Ensure that you have completed the Genomics Clinical Information Requisition Form (Form 20) prior to your appointment.
Test Details
Turnaround Time: Sample collection is available on Mondays and Thursdays by 9 am, with reports ready by Wednesdays and Saturdays.
Sample Type: 3 mL (2 mL min.) whole blood in 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Specialty: Hematology, Oncology
Department: Molecular Diagnostics
Method: Real Time PCR
Disease Type: Genetic Disorders
