FGG Gene Afibrinogenemia Congenital NGS Genetic DNA Test
Introduction to the Test
The FGG Gene Afibrinogenemia Congenital NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the FGG gene, which can lead to congenital afibrinogenemia. This rare bleeding disorder is characterized by a deficiency of fibrinogen in the blood, resulting in increased bleeding risk. Early diagnosis is crucial for effective management and treatment.
What the Test Measures
This test employs Next-Generation Sequencing (NGS) technology to detect genetic variations in the FGG gene. By analyzing the genetic material, healthcare providers can determine the presence of mutations that may cause congenital afibrinogenemia.
Who Should Consider This Test
Individuals who may benefit from the FGG Gene Afibrinogenemia Test include:
- Those with a family history of bleeding disorders.
- Patients experiencing unexplained bleeding or bruising.
- Individuals undergoing pre-surgical evaluations who may be at risk of bleeding complications.
Benefits of Taking the Test
Taking the FGG Gene Afibrinogenemia test offers several benefits:
- Accurate diagnosis of congenital afibrinogenemia.
- Guidance for management and treatment options.
- Informed decisions regarding family planning and genetic counseling.
Understanding Your Results
Results from the FGG Gene Afibrinogenemia test can provide valuable insights into your genetic health. A positive result indicates the presence of mutations associated with congenital afibrinogenemia, while a negative result suggests that no mutations were found. It is essential to discuss your results with a healthcare professional who can provide guidance and recommendations based on your individual situation.
Test Pricing
| Test Name | Discount Price (KSh) | Regular Price (KSh) |
|---|---|---|
| FGG Gene Afibrinogenemia Congenital NGS Genetic DNA Test | 40,000 | 56,000 |
Branches and Booking
We have branches across Kenya, including major cities such as Nairobi, Mombasa, and Kisumu. Our dedicated team is ready to assist you with the FGG Gene Afibrinogenemia Congenital NGS Genetic DNA Test.
To book the test, please call or WhatsApp us at +254711564616 today!
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient who is going for FGG Gene Afibrinogenemia, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGG Gene Afibrinogenemia.
- Specialty: Hematologist
- Department: Genetics
- Method: NGS Technology
- Disease Type: Hematology
