HBD Gene Thalassemia Delta NGS Genetic DNA Test
Introduction to the Test
The HBD Gene Thalassemia Delta NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the HBD gene associated with thalassemia. Thalassemia is a blood disorder characterized by reduced hemoglobin production, leading to anemia and various health complications. This test employs Next Generation Sequencing (NGS) technology, providing a comprehensive analysis of the genetic factors contributing to thalassemia.
What the Test Measures
This genetic test detects specific mutations within the HBD gene that can lead to thalassemia. By analyzing the DNA, healthcare providers can assess an individual’s risk of developing this condition and provide tailored management strategies.
Who Should Consider This Test?
Individuals with a family history of thalassemia or related symptoms, such as severe anemia, fatigue, or jaundice, should consider this test. Additionally, those who are carriers of thalassemia or belong to high-risk populations may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Early identification of genetic predispositions to thalassemia.
- Informed decision-making regarding family planning and management.
- Personalized treatment options based on genetic findings.
- Access to genetic counseling for better understanding and support.
Understanding Your Results
Your test results will indicate whether mutations are present in the HBD gene. A genetic counselor will help you interpret the results, discuss their implications, and guide you on potential next steps in terms of management and treatment.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| HBD Gene Thalassemia Delta NGS Genetic DNA Test | 400,000 | 560,000 |
Booking the Test
To ensure a timely and efficient testing process, please contact us to schedule your appointment. You can reach us at +2348077798758 for bookings or inquiries regarding the HBD Gene Thalassemia Delta NGS Genetic DNA Test.
Turnaround time for results is approximately 3 to 4 weeks. Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history and genetic counseling session is recommended to draw a pedigree chart of family members affected by HBD Gene Thalassemia.
