SFTPC Gene Surfactant metabolism dysfunction type 2 NGS Genetic Test
Short Name: SFTPC Gene Test
Also known as: Surfactant Protein C Deficiency, SFTPC Mutation Test
SFTPC Gene Surfactant metabolism dysfunction type 2 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 SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
To identify mutations in the SFTPC gene that cause surfactant metabolism dysfunction type 2, aiding in diagnosis, prognosis, and genetic counseling.
- Test Code
- 2258
- 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
Ensure no recent blood transfusions or bone marrow transplants. Provide clinical history and family pedigree.
Method: Venipuncture for blood sample
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist. For FTA card, a small drop of blood is applied.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Sample will be sent to the lab for analysis.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the SFTPC gene that cause surfactant metabolism dysfunction type 2, aiding in diagnosis, prognosis, and genetic counseling.
How to Prepare
- Use sterile techniques
- Label samples correctly
- Transport at ambient temperature
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"Early genetic testing for SFTPC mutations can guide treatment and family planning for surfactant metabolism dysfunction."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient sample volume
- Improper labeling
- Contaminated samples
Understanding Your Results
Confirms surfactant metabolism dysfunction type 2. Consult genetic counselor for management.
No pathogenic mutations detected. Consider other causes if symptoms persist.
Mutation detected but significance unknown. Requires further clinical and family studies.
If you experience symptoms like chronic cough, breathing difficulties, or have a family history of lung disorders, consult a healthcare provider for genetic testing.
Limitations
- ⚠May not detect all possible mutations
- ⚠Variants of uncertain significance require clinical correlation
- ⚠Does not assess other genes involved in lung surfactant disorders
Risks & Considerations
- ●Minor bruising or pain at blood draw site
- ●Very low risk of infection
Interfering Factors
- ●Hemolyzed or degraded DNA samples
- ●Contamination during sample collection
- ●Incorrect sample type or volume
Frequently Asked Questions
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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.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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