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FKTN Gene Walker-Warburg syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

FKTN Gene Walker-Warburg syndrome NGS Genetic Test

Short Name: FKTN Gene WWS NGS Test

Also known as: FKTN Gene Mutation Test, Walker-Warburg Syndrome Genetic Test, WWS NGS Test

FKTN Gene Walker-Warburg syndrome 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.

Next Generation Sequencing (NGS)Pediatric🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To identify mutations in the FKTN gene for accurate diagnosis of Walker-Warburg Syndrome, enabling early intervention and family planning.

Test Code
4608
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)
Step 1

Sample Collection

No special preparation required. Genetic counseling is recommended prior to testing.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn by a trained phlebotomist using sterile equipment.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Keep the area clean.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor to discuss the test, implications, and family history.
2
During the Test:Sample collection via blood draw and analysis using NGS technology.
3
After the Test:Receive the report online and discuss results with a physician or genetic counselor.

About This Test

Who Should Get This Test

To identify mutations in the FKTN gene for accurate diagnosis of Walker-Warburg Syndrome, enabling early intervention and family planning.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection tubes
  • Label samples correctly
  • Transport at ambient temperature

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Early genetic testing for Walker-Warburg Syndrome is crucial for timely intervention, family counseling, and informed decision-making."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture

Sample Stability

Blood sample stable at room temperature for 24 hours
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Contaminated sample
  • Incorrect labeling

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the FKTN gene associated with Walker-Warburg Syndrome.
📊

Pathogenic variant detected

Consistent with diagnosis of Walker-Warburg Syndrome. Genetic counseling and clinical management recommended.

📊

No pathogenic variant detected

Unlikely to have FKTN-related Walker-Warburg Syndrome. Consider other genetic or clinical evaluations.

⚠️ When to Consult a Doctor:

If symptoms of Walker-Warburg Syndrome are present, such as muscle weakness or developmental delays, or if there is a family history of the disorder.

Limitations

  • ⚠May not detect all types of mutations
  • ⚠Requires genetic counseling for interpretation
  • ⚠Results should be correlated with clinical findings

Risks & Considerations

  • ●Slight pain or bruising at the puncture site
  • ●Minimal risk of infection
  • ●Emotional impact of results

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA
  • ●Incorrect sample handling

Frequently Asked Questions

What is Walker-Warburg Syndrome?
Walker-Warburg Syndrome is a rare genetic disorder that affects brain and muscle development, often leading to severe symptoms in infancy.
What causes Walker-Warburg Syndrome?
It is caused by mutations in the FKTN gene, which is essential for producing a protein needed for normal tissue development.
What are the symptoms of Walker-Warburg Syndrome?
Symptoms include severe muscle weakness, hypotonia, developmental delay, intellectual disability, seizures, eye abnormalities, and brain malformations.
How is Walker-Warburg Syndrome diagnosed?
Diagnosis involves clinical evaluation and genetic testing, such as the FKTN Gene NGS Test, to identify mutations in the FKTN gene.
What is the FKTN gene?
The FKTN gene provides instructions for making a protein that is crucial for the normal development of muscle and brain tissues.
What is NGS genetic testing?
Next Generation Sequencing (NGS) is a advanced genetic testing method that can accurately detect mutations in genes, including the FKTN gene.
How is the FKTN Gene NGS Test performed?
The test involves extracting DNA from a blood or saliva sample and sequencing it using NGS technology to identify mutations.
What is the cost of the FKTN Gene Walker-Warburg Syndrome NGS Test?
The test costs INR 20,000 at DNA Labs India, with home sample collection available.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across many cities in India.
How long does it take to get the results?
Results are typically available within 3 to 4 weeks after sample collection.
What should I do if the test is positive?
If a pathogenic variant is detected, consult a healthcare provider for genetic counseling and management options.
Is genetic counseling necessary?
Yes, genetic counseling is recommended before and after testing to understand the implications and support decision-making.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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For Hospitals & Clinics

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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✓ 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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