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DNA Labs India

VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic Test

Short Name: VSX1 Gene NGS Test

VSX1 Gene Craniofacial anomalies and anterior segment dysgenesis syndrome NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses 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.

PediatricsPediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify mutations in the VSX1 gene that cause craniofacial anomalies and anterior segment dysgenesis syndrome, aiding in diagnosis, treatment planning, and genetic counseling.

Test Code
2713
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
Step 1

Sample Collection

Clinical history review and genetic counseling session recommended to draw a pedigree chart of family members.

Step 2

Laboratory Analysis

Your sample is analyzed using NGS 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 assessment.
2
During the Test:Blood sample collection for DNA extraction and NGS analysis.
3
After the Test:Report generation and genetic counseling for result interpretation.

About This Test

Who Should Get This Test

To identify mutations in the VSX1 gene that cause craniofacial anomalies and anterior segment dysgenesis syndrome, aiding in diagnosis, treatment planning, and genetic counseling.

How to Prepare

  • Collect blood sample in appropriate container
  • Ensure proper labeling and transport

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the VSX1 gene.
📊

Positive

Pathogenic variant detected, indicating genetic cause for symptoms.

📊

Negative

No pathogenic variants detected, but clinical correlation is advised.

⚠️ When to Consult a Doctor:

If you experience symptoms such as corneal opacities, glaucoma, cataracts, or craniofacial abnormalities, consult a healthcare professional for evaluation.

Frequently Asked Questions

What is the VSX1 gene?
The VSX1 gene provides instructions for making a protein involved in the development of the eye and face. Mutations in this gene can lead to craniofacial anomalies and anterior segment dysgenesis syndrome.
What conditions are associated with VSX1 gene mutations?
VSX1 gene mutations are associated with craniofacial anomalies (abnormalities in face and skull development) and anterior segment dysgenesis syndrome (a disorder affecting the front part of the eye).
What are the symptoms of VSX1 gene-related disorders?
Symptoms may include corneal opacities, glaucoma, cataracts, abnormalities in eye shape and size, facial and skull deformities, reduced vision, and eye pain or discomfort.
How is the VSX1 gene test performed?
The test uses Next-Generation Sequencing (NGS) technology to analyze DNA from a blood sample or extracted DNA for mutations in the VSX1 gene.
What is the cost of the VSX1 gene test in India?
The cost of the VSX1 Gene NGS Genetic Test at DNA Labs India is INR 20000, with free home sample collection available across India.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for the VSX1 gene test in numerous cities across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates the detection of a pathogenic variant in the VSX1 gene, which may be the genetic cause of symptoms. Genetic counseling is recommended.
What does a negative result mean?
A negative result means no pathogenic variants were detected in the VSX1 gene. However, clinical correlation with symptoms is advised, as other genetic factors may be involved.
Is genetic counseling recommended before and after the test?
Yes, genetic counseling is recommended to discuss the implications of testing, interpret results, and provide guidance for family planning and management.
Can this test be used for prenatal diagnosis?
This test is primarily for diagnostic purposes in individuals with symptoms. For prenatal diagnosis, consult a genetic counselor for appropriate testing options.
What are the treatment options for VSX1 gene disorders?
Treatment focuses on managing symptoms, such as surgical interventions for eye anomalies, vision correction, and regular monitoring. Genetic counseling can help with family planning.
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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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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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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