FKTN Gene Cardiomyopathy, dilated type 1X NGS Genetic Test
Short Name: FKTN Cardiomyopathy NGS Test
Also known as: FKTN-related dilated cardiomyopathy genetic test, FKTN gene mutation analysis, Cardiomyopathy type 1X NGS test
FKTN Gene Cardiomyopathy, dilated type 1X 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 from sample receipt. 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 diagnose dilated cardiomyopathy caused by mutations in the FKTN gene, aiding in early detection, family screening, and personalized treatment planning.
- Test Code
- 5227
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks from sample receipt
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Venipuncture or finger-prick
Laboratory Analysis
A blood sample will be drawn from a vein in the arm or a saliva sample collected using a kit.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Resume normal activities.
Timeline: 3 to 4 weeks from sample receipt
Patient Instructions
About This Test
Who Should Get This Test
To diagnose dilated cardiomyopathy caused by mutations in the FKTN gene, aiding in early detection, family screening, and personalized treatment planning.
How to Prepare
- Ensure proper identification
- Use sterile collection equipment
- Label samples correctly
- Transport samples at recommended temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This NGS genetic test is essential for identifying FKTN gene mutations linked to dilated cardiomyopathy, enabling early intervention and family screening."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improper labeling or storage
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of FKTN-related dilated cardiomyopathy. Recommend cardiac evaluation and family screening.
Negative for pathogenic variant
No mutations detected in FKTN gene. Consider other genetic or non-genetic causes if symptoms persist.
Variant of uncertain significance (VUS)
Genetic variant identified but clinical significance unclear. Follow-up and genetic counseling advised.
Consult a cardiologist or geneticist immediately if test results are positive or if symptoms worsen. Regular follow-up is recommended for monitoring.
Limitations
- ⚠Test may not detect all genetic variants
- ⚠Results require clinical correlation
- ⚠Limited to FKTN gene analysis only
Risks & Considerations
- ●Minimal risk from blood draw: bruising, infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Recent blood transfusions may affect results
Compare With Similar Tests
| Test | FKTN Gene Cardiomyopathy, dilated type 1X NGS Genetic Test | TTN Gene Cardiomyopathy Test | LMNA Gene Cardiomyopathy Test | Cardiac MRI | Echocardiogram |
|---|---|---|---|---|---|
| Comparison | FKTN Gene Cardiomyopathy, dilated type 1X NGS Genetic Test | Focuses on TTN gene mutations; often used alongside FKTN test for comprehensive diagnosis. | Detects LMNA gene mutations; relevant for different cardiomyopathy subtypes. | Imaging test for structural assessment; complements genetic testing. | Evaluates heart function; used in conjunction with genetic tests for diagnosis. |
Frequently Asked Questions
What is the FKTN Gene Cardiomyopathy NGS Genetic Test?
Who should get this test?
How is the test performed?
What is the cost of the test?
Is home sample collection available?
How long does it take to get results?
What do the results mean?
Are there any risks to the test?
Can this test diagnose other types of cardiomyopathy?
Is genetic counseling included?
What should I do before the test?
How accurate is the test?
Related Tests
MMC (Maternal Myopathy with Cardiomyopathy) Mutation Detection Test
₹11,500LPA Gene Coronary artery disease, susceptibility to NGS Genetic Test
₹20,000ITIH4 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test
₹20,000PPP1R17 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test
₹20,000APOA1 Gene Hypoalphalipoproteinemia NGS Genetic Test
₹20,000GJC2 Gene Lymphedema, hereditary, type IC NGS Genetic Test
₹20,000Reference 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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.