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FERMT1 Gene Kindler syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

FERMT1 Gene Kindler syndrome NGS Genetic Test

Short Name: Kindler Syndrome NGS Test

Also known as: FERMT1 Mutation Analysis, Kindler Syndrome Genetic Test, Kindlin-1 Gene Test

FERMT1 Gene Kindler syndrome 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.

NGS Genetic Test🏠 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

The purpose of the FERMT1 Gene Kindler Syndrome NGS Genetic Test is to identify mutations in the FERMT1 gene that cause Kindler Syndrome. This test aids in definitive diagnosis, guides treatment plans, enables family genetic counseling, and helps assess the risk of complications such as skin cancer.

Test Code
5042
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
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Kindler Syndrome.

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review are required before sample collection.
2
During the Test:Sample collection via blood draw or FTA card.
3
After the Test:Results are delivered in 3 to 4 weeks via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

The purpose of the FERMT1 Gene Kindler Syndrome NGS Genetic Test is to identify mutations in the FERMT1 gene that cause Kindler Syndrome. This test aids in definitive diagnosis, guides treatment plans, enables family genetic counseling, and helps assess the risk of complications such as skin cancer.

How to Prepare

  • Provide clinical history and undergo genetic counseling.
  • Sample can be blood, extracted DNA, or one drop of blood on an FTA card.
  • No fasting required.

Doctor's Notes

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

"Early genetic testing for Kindler Syndrome is crucial for timely management and family counseling. The FERMT1 gene test provides definitive diagnosis."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the FERMT1 gene. A positive result confirms Kindler Syndrome, while a negative result may require further clinical evaluation.
📊

Positive for pathogenic variant

Confirms diagnosis of Kindler Syndrome. Genetic counseling recommended.

📊

Negative for pathogenic variant

No mutations detected in the FERMT1 gene. Clinical correlation advised.

📊

Variant of uncertain significance

Further testing or family studies may be needed.

⚠️ When to Consult a Doctor:

Consult a healthcare provider if symptoms such as skin blistering, pigmentation changes, or other signs of Kindler Syndrome appear, especially in infancy or early childhood.

Limitations

  • ⚠Test may not detect all possible mutations in the FERMT1 gene.
  • ⚠Results should be interpreted in conjunction with clinical findings.

Risks & Considerations

  • ●Minimal risk associated with blood draw, such as bruising or infection.
  • ●Genetic testing may have psychological implications; counseling is advised.

Frequently Asked Questions

What is Kindler Syndrome?
Kindler Syndrome is a rare genetic disorder affecting the skin, mucous membranes, and internal organs, caused by mutations in the FERMT1 gene.
What causes Kindler Syndrome?
It is caused by mutations in the FERMT1 gene, which leads to defective kindlin-1 protein, disrupting cell function in skin and tissues.
How is Kindler Syndrome diagnosed?
Diagnosis involves physical exam, medical history, skin biopsy, and genetic testing like the FERMT1 Gene NGS Test.
What does the NGS Genetic Test involve?
The test uses next-generation sequencing to analyze DNA from blood or saliva for mutations in the FERMT1 gene.
How much does the FERMT1 Gene Test cost?
The cost is INR 20000.0 at DNA Labs India, with free home sample collection across India.
Is home sample collection available?
Yes, free home collection is available in numerous cities across India for online bookings.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
What are the symptoms of Kindler Syndrome?
Symptoms include skin blistering, pigmentation changes, increased skin cancer risk, eye and oral problems, and gastrointestinal issues.
Can Kindler Syndrome be treated?
There is no cure, but management focuses on symptom relief, wound care, and monitoring for complications like skin cancer.
Is the test covered by insurance?
Coverage varies; it is not typically covered under government schemes like PMJAY, but check with private insurers.
How accurate is the NGS Genetic Test?
The test is highly accurate for detecting mutations in the FERMT1 gene, but results should be interpreted clinically.
Who should consider this test?
Individuals with symptoms of Kindler Syndrome or a family history of the disorder should consider genetic testing.
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.

LIMS Integration

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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