Skip to main content
DNA Labs India

FOXC1 Gene Axenfeld-Rieger syndrome type 3 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

FOXC1 Gene Axenfeld-Rieger syndrome type 3 NGS Genetic Test

Short Name: FOXC1 ARS Type 3 NGS Test

Also known as: Axenfeld-Rieger Syndrome Type 3 Genetic Test, FOXC1 Gene Mutation Test

FOXC1 Gene Axenfeld-Rieger syndrome type 3 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

To detect mutations in the FOXC1 gene for accurate diagnosis of Axenfeld-Rieger Syndrome Type 3, facilitating early management and genetic counseling.

Test Code
5661
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 review and genetic counseling session required to draw a pedigree chart of affected family members.

Method: Venipuncture or blood drop on FTA card

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or one drop on FTA card at ambient room temperature.

Step 3

Report Delivery

Sample labeled and sent to the laboratory for NGS analysis.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling session and clinical history review to assess indications and draw a family pedigree chart.
2
During the Test:Blood sample collection and processing for NGS analysis in the laboratory.
3
After the Test:Result interpretation by geneticists, followed by counseling and report delivery.

About This Test

Who Should Get This Test

To detect mutations in the FOXC1 gene for accurate diagnosis of Axenfeld-Rieger Syndrome Type 3, facilitating early management and genetic counseling.

How to Prepare

  • Ensure proper sample collection technique
  • Label samples with patient details accurately
  • Store at ambient temperature as specified

Doctor's Notes

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

"This test is crucial for early diagnosis and management of Axenfeld-Rieger Syndrome Type 3, aiding in genetic counseling and family planning to address eye, dental, and facial abnormalities."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or blood drop on FTA card

Sample Stability

Blood samples stable at ambient temperature for 24 hours
FTA cards stable for extended periods at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improper labeling or storage

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the FOXC1 gene, aiding in diagnosis of Axenfeld-Rieger Syndrome Type 3.
📊

Mutation detected

Confirms diagnosis of Axenfeld-Rieger Syndrome Type 3; genetic counseling recommended for management and family planning.

📊

No mutation detected

Unlikely to have the syndrome based on genetic testing, but clinical correlation is advised if symptoms persist.

⚠️ When to Consult a Doctor:

If symptoms such as eye abnormalities, dental issues, or facial dysmorphism are present, or if there is a family history of Axenfeld-Rieger Syndrome, consult a geneticist or ophthalmologist.

Limitations

  • ⚠May not detect all types of genetic variations
  • ⚠Requires clinical correlation and genetic counseling for interpretation

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection
  • ●Potential psychological impact of genetic results

Interfering Factors

  • ●Poor sample quality
  • ●Contamination during collection or processing

Compare With Similar Tests

TestFOXC1 Gene Axenfeld-Rieger syndrome type 3 NGS Genetic Test
ComparisonFOXC1 Gene Axenfeld-Rieger syndrome type 3 NGS Genetic Test

Frequently Asked Questions

What is FOXC1 Gene Axenfeld-Rieger Syndrome Type 3?
It is a rare genetic disorder caused by mutations in the FOXC1 gene, affecting eye, teeth, and facial development.
What are the common symptoms of this syndrome?
Symptoms include glaucoma, cataracts, iris abnormalities, missing or extra teeth, and facial features like a flattened mid-face.
How is Axenfeld-Rieger Syndrome Type 3 diagnosed?
Diagnosis involves clinical evaluation and genetic testing to confirm FOXC1 gene mutations.
What does the NGS Genetic Test involve?
It uses Next-Generation Sequencing technology to analyze the FOXC1 gene for mutations from a blood or DNA sample.
What is the cost of the FOXC1 Gene test?
The test costs INR 20000, including genetic counseling and result interpretation.
Is home sample collection available for this test?
Yes, free home sample collection is available for online bookings across many cities in India.
How long does it take to get the test results?
Results are typically available in 3 to 4 weeks.
What do the test results indicate?
Results show the presence or absence of FOXC1 gene mutations, helping confirm or rule out the syndrome.
Is genetic counseling included with the test?
Yes, genetic counseling is included to help understand results and implications for family planning.
Who should consider getting this genetic test?
Individuals with symptoms of Axenfeld-Rieger Syndrome, a family history, or those seeking early detection for at-risk family members.
Are there any risks associated with the test?
Risks are minimal, mainly related to blood draw, such as bruising, and potential psychological impact of results.
How can I book the FOXC1 Gene test?
You can book online through DNA Labs India's website or contact them via phone or WhatsApp for assistance.
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.

Related Tests

Amino Acids Qualitative Two Dimensional Urine Test

₹1,439

Succinylacetone Urine Test

₹5,000

RXFP2 Gene Cryptorchidism NGS Genetic Test

₹20,000

EFNB1 Gene Craniofrontonasal syndrome NGS Genetic Test

₹20,000

MNX1 Gene Currarino syndrome NGS Genetic Test

₹20,000

FGFR1 Gene Craniosynostosis, FGFR1 related NGS Genetic Test

₹20,000
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.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.