FGB Gene Afibrinogenemia Congenital NGS Genetic DNA Test
Introduction
The FGB Gene Afibrinogenemia Congenital NGS Genetic DNA Test is a pioneering diagnostic tool that plays a vital role in identifying genetic mutations linked to Afibrinogenemia. This condition, characterized by a deficiency of fibrinogen, can lead to severe bleeding disorders. Understanding the genetic basis of this condition is crucial for effective management and treatment, making this test an essential component of personalized healthcare.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the FGB gene, which is responsible for coding the fibrinogen protein. By identifying mutations in this gene, healthcare providers can better understand a patient’s risk for developing Afibrinogenemia and related complications.
Who Should Consider This Test
Individuals with a family history of bleeding disorders, unexplained bleeding episodes, or those who have been diagnosed with Afibrinogenemia should consider this test. Symptoms may include:
- Frequent nosebleeds
- Unusual bruising
- Heavy menstrual bleeding
- Prolonged bleeding after injury or surgery
Benefits of Taking the Test
Taking the FGB Gene Afibrinogenemia Congenital NGS Genetic DNA Test offers several benefits:
- Early detection of genetic mutations.
- Informed decision-making regarding treatment options.
- Access to genetic counseling for affected family members.
- Better management of bleeding risks.
Understanding Your Results
Results from the FGB Gene Afibrinogenemia test will provide insights into whether mutations are present in the FGB gene. A genetic counselor will help interpret these results and discuss potential implications for you and your family.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| FGB Gene Afibrinogenemia Congenital NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the FGB Gene Afibrinogenemia Congenital NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any questions you may have.
Additional Information
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by Afibrinogenemia.
- Specialty: Hematology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Hematology
