Beta Thalassemia HBB Full Gene Analysis Single
Introduction to Beta Thalassemia HBB Full Gene Analysis
The Beta Thalassemia HBB Full Gene Analysis Single test is a vital diagnostic tool designed to evaluate genetic mutations associated with beta thalassemia, a hereditary blood disorder characterized by reduced hemoglobin production. This test is essential for individuals with a family history of thalassemia or those exhibiting symptoms of anemia. Understanding your genetic predisposition can significantly impact your health management.
What the Test Measures
This test specifically analyzes the HBB gene, which is responsible for producing the beta-globin subunit of hemoglobin. It detects mutations that may lead to beta thalassemia, allowing for accurate diagnosis and management of the condition.
Who Should Consider This Test?
- Individuals with a family history of beta thalassemia.
- Patients experiencing unexplained anemia or fatigue.
- Those planning to conceive or undergo genetic counseling.
- Individuals with risk factors such as Mediterranean, African, or Asian ancestry.
Benefits of Taking the Test
- Accurate diagnosis of beta thalassemia.
- Informed family planning and genetic counseling.
- Early detection allows for proactive management of health.
- Helps in understanding potential treatment options.
Understanding Your Results
Results from the Beta Thalassemia HBB Full Gene Analysis will indicate whether any mutations are present in the HBB gene. A genetic counselor or healthcare provider will help interpret these results and discuss potential implications for your health and family.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Beta Thalassemia HBB Full Gene Analysis Single | 150,000 NGN | 200,000 NGN |
Booking the Test
To book the Beta Thalassemia HBB Full Gene Analysis Single test, please contact us at +2348077798758 via call or WhatsApp. Remember, a doctor’s prescription is required for this test, except for cases involving surgery, pregnancy, or individuals planning to travel abroad.
Additional Information
Turnaround time for results is approximately 8-10 days, and the sample type required is peripheral blood collected in an EDTA Vacutainer (2ml). This test utilizes Sanger sequencing, a highly accurate method for gene analysis.
