FGG Gene Afibrinogenemia, congenital NGS Genetic Test
Short Name: FGG Gene Afibrinogenemia Test
Also known as: FGG Gene Mutation Test, Congenital Afibrinogenemia Genetic Test, Fibrinogen Gamma Chain Gene Test
FGG Gene Afibrinogenemia, congenital NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of the FGG Gene Afibrinogenemia NGS Genetic Test is to identify mutations in the FGG gene that cause congenital afibrinogenemia, enabling accurate diagnosis and personalized management of this bleeding disorder.
- Test Code
- 5561
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required. Inform the lab about any medications or supplements.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn from a vein in your arm.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Resume normal activities.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the FGG Gene Afibrinogenemia NGS Genetic Test is to identify mutations in the FGG gene that cause congenital afibrinogenemia, enabling accurate diagnosis and personalized management of this bleeding disorder.
How to Prepare
- Bring identification and prescription
- Wear loose clothing for easy access
- Follow any specific instructions from the lab
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for FGG gene mutations is essential for confirming congenital afibrinogenemia, allowing for early intervention and management of bleeding risks."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Incorrect labeling
Understanding Your Results
No pathogenic mutations detected
Normal, no afibrinogenemia due to FGG gene mutations
Pathogenic mutations detected
Confirms congenital afibrinogenemia, genetic counseling recommended
If you experience unexplained bleeding symptoms or have a family history of bleeding disorders, consult a hematologist or geneticist.
Limitations
- ⚠May not detect all types of mutations
- ⚠Results require genetic counseling
- ⚠Not a substitute for clinical diagnosis
Risks & Considerations
- ●Minimal risk from blood draw: bruising, infection at puncture site
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Incorrect sample collection
Compare With Similar Tests
| Test | FGG Gene Afibrinogenemia, congenital NGS Genetic Test | Fibrinogen Level Test | Coagulation Panel |
|---|---|---|---|
| Comparison | FGG Gene Afibrinogenemia, congenital NGS Genetic Test | Measures fibrinogen levels but does not identify genetic mutations | Assesses overall clotting function but not specific to FGG gene |
Frequently Asked Questions
What is the FGG Gene Afibrinogenemia Test?
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What sample is required for the test?
Is fasting required before the test?
How long does it take to get results?
Is home sample collection available?
What are the symptoms of afibrinogenemia?
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Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
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