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DNA Labs India

WFS1 Gene Wolfram-like syndrome, autosomal dominant NGS Genetic Test

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WFS1 Gene Wolfram-like syndrome, autosomal dominant NGS Genetic Test

Short Name: WFS1 Gene Wolfram-like Syndrome Test

Also known as: Wolfram-like syndrome, WFS1-related disorder, Autosomal dominant Wolfram-like syndrome

WFS1 Gene Wolfram-like syndrome, autosomal dominant 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.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect mutations in the WFS1 gene to confirm a diagnosis of Wolfram-like syndrome, guide treatment decisions, and provide information for genetic counseling and family planning.

Test Code
4797
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 specific preparation required. Inform the lab about any medications or recent blood transfusions.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in your arm by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:No special preparation needed. Ensure to provide accurate clinical history.
2
During the Test:The test involves a simple blood draw. The process is quick and minimally invasive.
3
After the Test:You can resume normal activities immediately. Results will be available in 3-4 weeks.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the WFS1 gene to confirm a diagnosis of Wolfram-like syndrome, guide treatment decisions, and provide information for genetic counseling and family planning.

How to Prepare

  • Bring a valid ID and prescription
  • Wear loose clothing for easy access to arm
  • Stay hydrated before the test

Doctor's Notes

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

"Early genetic testing for WFS1 mutations can aid in timely management of Wolfram-like syndrome, especially in families with a history of the disorder."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood
ContainerEDTA tube
Collection MethodVenipuncture

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods at -20°C
Sample Rejection Criteria:
  • Hemolyzed or lipemic sample
  • Insufficient sample volume
  • Incorrect sample type

Understanding Your Results

Results of the WFS1 gene test indicate whether pathogenic mutations are present. A positive result confirms Wolfram-like syndrome, while a negative result may not rule out other causes.
📊

Positive for pathogenic mutation

Confirms diagnosis of Wolfram-like syndrome. Genetic counseling recommended.

📊

Negative for pathogenic mutation

No mutations detected in WFS1 gene. Clinical correlation advised.

📊

Variant of uncertain significance

Further testing or family studies may be needed.

⚠️ When to Consult a Doctor:

Consult a geneticist or your physician if you have symptoms of Wolfram-like syndrome or a family history of the disorder. After testing, discuss results with a healthcare provider for appropriate management.

Limitations

  • May not detect all types of mutations
  • Requires interpretation by a geneticist
  • Results should be correlated with clinical findings

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection at the puncture site

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Hemolyzed blood sample

Frequently Asked Questions

What is Wolfram-like syndrome?
Wolfram-like syndrome is a rare genetic disorder affecting the nervous and endocrine systems, caused by mutations in the WFS1 gene.
What causes Wolfram-like syndrome?
It is caused by mutations in the WFS1 gene, which provides instructions for making the wolframin protein.
What are the symptoms of Wolfram-like syndrome?
Symptoms include vision problems, hearing loss, diabetes mellitus, urinary tract issues, neurological problems, and psychiatric symptoms.
How is Wolfram-like syndrome diagnosed?
Diagnosis involves clinical evaluation, family history, and genetic testing such as the WFS1 gene NGS test.
What is the WFS1 gene test?
It is a next-generation sequencing (NGS) test that analyzes the WFS1 gene for mutations associated with Wolfram-like syndrome.
How much does the WFS1 gene test cost in India?
The cost is approximately INR 20,000 at DNA Labs India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What does a positive result mean?
A positive result confirms the presence of pathogenic mutations in the WFS1 gene, indicating Wolfram-like syndrome.
What does a negative result mean?
A negative result means no pathogenic mutations were detected, but clinical correlation is advised.
Is genetic counseling provided?
Yes, genetic counseling is included as part of the test service at DNA Labs India.
How can I book the test?
You can book the test online through the DNA Labs India website or contact them via phone or WhatsApp.
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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