Sickle Cell Disease Mutation Screening
Introduction
The Sickle Cell Disease Mutation Screening is a vital genetic test designed to detect specific mutations in the hemoglobin gene that can lead to sickle cell disease. This condition affects millions worldwide, particularly in regions where malaria is prevalent. Understanding your genetic predisposition to this disease is crucial for early intervention and management.
What the Test Measures
This test measures the presence of mutations in the HBB gene, which encodes the beta-globin subunit of hemoglobin. By identifying these mutations, healthcare providers can determine an individual’s risk of developing sickle cell disease or being a carrier of the trait.
Who Should Consider This Test
Individuals who should consider this test include:
- Those with a family history of sickle cell disease.
- Individuals experiencing symptoms such as severe pain, anemia, or frequent infections.
- Pregnant women or couples planning to have children, especially if they belong to high-risk ethnic groups.
- People planning to travel abroad to regions where sickle cell disease is prevalent.
Benefits of Taking the Test
Taking the Sickle Cell Disease Mutation Screening offers several benefits:
- Early detection of genetic predisposition to sickle cell disease.
- Informed family planning decisions for couples at risk.
- Guidance on management and treatment options for those identified as carriers or affected.
- Peace of mind for individuals and families regarding their genetic health.
Understanding Your Results
Results from the Sickle Cell Disease Mutation Screening will indicate whether mutations are present. A healthcare provider will assist in interpreting the results and discussing the implications for your health and that of your family.
Test Details and Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
Sickle Cell Disease Mutation Screening | 105,000 NGN | 140,000 NGN |
Booking Your Test
To book your Sickle Cell Disease Mutation Screening, please call or WhatsApp us at +2348077798758. This test requires a Doctor’s prescription, which is not applicable for surgery and pregnancy cases or individuals planning to travel abroad. The turnaround time for results is approximately 3-4 days, and the sample type required is peripheral blood collected in an EDTA Vacutainer (2 ml).
Don’t wait to understand your genetic health. Schedule your test today and take a proactive step towards your well-being!