Blood Coagulation Panel NGS Genetic DNA Test
Introduction
The Blood Coagulation Panel NGS Genetic DNA Test is a state-of-the-art diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze genetic predispositions related to blood coagulation. This test is vital for identifying potential genetic disorders that can lead to abnormal blood clotting, which may result in serious health complications.
What the Test Measures
This test evaluates genetic variations associated with various coagulation factors, including but not limited to ACTN1, ACVRL1, ADAMTS13, and F2. By analyzing these genetic markers, the test can identify inherited conditions that may predispose individuals to thrombotic events or bleeding disorders.
Who Should Consider This Test
Individuals with a family history of blood clotting disorders, recurrent miscarriages, or unexplained bleeding should consider undergoing the Blood Coagulation Panel NGS Genetic DNA Test. Symptoms such as easy bruising, prolonged bleeding after injuries, or unusual blood clotting may also warrant this genetic assessment.
Benefits of Taking the Test
- Identifies genetic risk factors for blood coagulation disorders.
- Informs personalized treatment and management plans.
- Provides peace of mind for patients and their families.
- Enables proactive healthcare decisions to prevent complications.
Understanding Your Results
Results from the Blood Coagulation Panel NGS Genetic DNA Test will be interpreted by qualified hematologists and genetic counselors. They will provide guidance on the implications of your results, potential next steps, and any necessary lifestyle changes or treatments.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 600,000 NGN |
Book the Test
To book your Blood Coagulation Panel NGS Genetic DNA Test, please call or WhatsApp us at +2348110567037. Take charge of your health today by understanding your genetic predispositions!
Additional Information
Turnaround time for results is approximately 3 to 4 weeks, and the sample type required for this test can be blood or extracted DNA, or even one drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to gather a clinical history and draw a pedigree chart of affected family members.
Our dedicated team of hematologists and genetic specialists are here to support you throughout the testing process and beyond.
