FLI1 Gene Platelet dense granule secretion defect, excessive bleeding NGS Genetic Test
Short Name: FLI1 Gene NGS Genetic Test
Also known as: FLI1 Gene Disorder, Platelet Dense Granule Secretion Defect
FLI1 Gene Platelet dense granule secretion defect, excessive bleeding NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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
To detect mutations in the FLI1 gene that cause platelet dense granule secretion defect, leading to excessive bleeding disorders.
- Test Code
- 5617
- 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
- NGS Technology
Sample Collection
Clinical history review and genetic counseling session recommended to draw a pedigree chart of family members.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample collected via venipuncture or using an FTA card with one drop of blood.
Report Delivery
Sample is labeled, stored at ambient room temperature, and sent to the laboratory for analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the FLI1 gene that cause platelet dense granule secretion defect, leading to excessive bleeding disorders.
How to Prepare
- Ensure proper sample handling to avoid contamination
- Label samples with patient details accurately
- Use provided FTA card if applicable
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for diagnosing inherited bleeding disorders and guiding treatment, especially in cases of unexplained excessive bleeding."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Incorrect labeling or missing information
Understanding Your Results
Positive
Mutation detected in FLI1 gene, consistent with platelet dense granule secretion defect. Clinical correlation and genetic counseling advised.
Negative
No mutation detected in FLI1 gene. However, clinical symptoms may still be present due to other causes; further evaluation recommended.
If symptoms of excessive bleeding persist, worsen, or if there is a family history of bleeding disorders, consult a hematologist or genetic specialist.
Limitations
- ⚠Test only detects mutations in the FLI1 gene
- ⚠Does not rule out other causes of bleeding disorders
- ⚠Results require clinical correlation
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Genetic implications for family members may require counseling
Interfering Factors
- ●Poor sample quality
- ●Contamination during collection
- ●Improper sample storage
Frequently Asked Questions
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