Thalassemia Beta Complete Gene Analysis With MCC Test
Introduction to the Test
The Thalassemia Beta Complete Gene Analysis With MCC Test is a vital diagnostic tool used to identify genetic mutations associated with beta-thalassemia. This disorder affects hemoglobin production, leading to anemia and other serious health complications. Understanding your genetic predisposition can be crucial for effective management and treatment.
What the Test Measures
This test specifically analyzes the HBB gene, which is responsible for producing the beta chains of hemoglobin. By utilizing advanced Next Generation Sequencing and Fragment analysis methods, the test detects variations or mutations that may indicate beta-thalassemia.
Who Should Consider This Test?
Individuals who should consider this test include:
- Expectant parents with a family history of thalassemia.
- Individuals experiencing symptoms of anemia, such as fatigue or weakness.
- People of Mediterranean, African, or Asian descent, as they are at higher risk for thalassemia.
Benefits of Taking the Test
Understanding your genetic makeup through this test can provide several benefits:
- Early detection of potential health issues.
- Informed family planning decisions for couples at risk of passing on genetic disorders.
- Guidance for treatment options and management strategies.
Understanding Your Results
Once the test is complete, you will receive a detailed report outlining any genetic variations detected. It is essential to discuss these results with a healthcare professional who can provide context and guidance on the next steps.
Test Name and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Thalassemia Beta Complete Gene Analysis With MCC Test | 420,000 NGN | 560,000 NGN |
Booking the Test
To book the Thalassemia Beta Complete Gene Analysis With MCC Test, please contact us at +2348077798758 or visit our website. Ensure you have the necessary forms filled out, including the Prenatal Genetic Testing Consent Form (Form 18) and the Genomics Clinical Information Requisition Form (Form 20), as these are mandatory for processing your sample.
Test Parameters
Turnaround Time: Sample Daily by 9 am; Report in 21 Working Days
Sample Type: Submit 3 mL (2 mL min.) whole blood (Maternal) in 1 Lavender top (EDTA) tube AND 10 mL (5 mL min.) Amniotic fluid / CVS in a sterile screw-capped container. Ship refrigerated. DO NOT FREEZE.
Test Components: HBB gene
Pre-Test Instructions: Duly filled Prenatal Genetic Testing Consent Form (Form 18) & Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Specialty: Hematology
Department: Molecular Diagnostics
Method: Next Generation Sequencing, Fragment Analysis
Disease Type: Genetic Disorders
