Sale!

PITX3 Gene Anterior Segment Mesenchymal Dysgenesis NGS Genetic DNA Test

Original price was: $700.Current price is: $500.

-29%

The PITX3 Gene Anterior Segment Mesenchymal Dysgenesis NGS Genetic DNA Test is a cutting-edge genetic analysis that identifies mutations in the PITX3 gene responsible for anterior segment mesenchymal dysgenesis. This comprehensive test utilizes Next Generation Sequencing (NGS) technology to detect genetic variations that affect eye development, particularly the anterior segment structures including the cornea, iris, and lens. Individuals with family history of congenital eye abnormalities, Peters anomaly, or anterior segment dysgenesis should consider this test. The test provides crucial information for accurate diagnosis, genetic counseling, and personalized treatment planning. Results are typically available within 3-4 weeks from blood or DNA samples. The test is priced at $500 USD with a regular price of $700 USD, offering significant savings for comprehensive genetic analysis.

Clinically Validated & Lab Certified

  • ISO-Accredited Laboratory, Ensuring Highest Standards
  • Trusted by Hospitals & Patients —Accredited Testing with Results
  • Direct Healthcare Provider Support + Comprehensive Reporting
Guaranteed Safe Checkout

PITX3 Gene Anterior Segment Mesenchymal Dysgenesis NGS Genetic DNA Test

Comprehensive Genetic Analysis for Eye Development Disorders

The PITX3 Gene Anterior Segment Mesenchymal Dysgenesis NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for congenital eye disorders. This advanced test specifically targets mutations in the PITX3 gene, which plays a critical role in the development of anterior segment structures during embryonic formation. Anterior segment mesenchymal dysgenesis encompasses a spectrum of conditions affecting the front portion of the eye, including the cornea, iris, and lens development.

What Does This Test Measure and Detect?

Our comprehensive NGS-based genetic test analyzes the complete coding region of the PITX3 gene to identify:

  • Point mutations and single nucleotide variations
  • Small insertions and deletions (indels)
  • Copy number variations affecting the PITX3 gene
  • Regulatory region mutations impacting gene expression
  • Novel genetic variants associated with anterior segment development

The test utilizes state-of-the-art Next Generation Sequencing technology, providing unparalleled accuracy and comprehensive coverage of the PITX3 gene region. This advanced methodology ensures detection of even rare genetic variants that might be missed by conventional testing methods.

Who Should Consider This Genetic Test?

This specialized genetic test is recommended for individuals presenting with:

  • Congenital eye abnormalities affecting anterior segment structures
  • Family history of Peters anomaly or anterior segment dysgenesis
  • Unexplained congenital cataracts with anterior segment involvement
  • Developmental abnormalities of the iris or cornea
  • Suspected genetic predisposition to eye development disorders
  • Children with multiple congenital eye anomalies
  • Individuals with affected family members requiring genetic counseling

Clinical Benefits of PITX3 Genetic Testing

Undergoing PITX3 genetic testing provides numerous clinical advantages:

  • Accurate Diagnosis: Confirms genetic basis of anterior segment dysgenesis
  • Personalized Treatment Planning: Enables targeted therapeutic approaches
  • Genetic Counseling: Provides essential information for family planning
  • Early Intervention: Facilitates timely management of associated conditions
  • Prognostic Information: Helps predict disease progression and outcomes
  • Research Contribution: Advances understanding of genetic eye disorders

Understanding Your Test Results

Our comprehensive genetic report provides detailed interpretation of your results:

  • Positive Result: Indicates presence of pathogenic mutation in PITX3 gene, confirming genetic diagnosis of anterior segment mesenchymal dysgenesis
  • Negative Result: Suggests absence of detectable mutations in PITX3 gene, though other genetic factors may be involved
  • Variant of Uncertain Significance: Identifies genetic changes with unclear clinical impact, requiring further evaluation
  • Carrier Status: Determines if individuals carry mutations without showing symptoms

All results are accompanied by detailed clinical interpretation and recommendations from our board-certified genetic specialists. Genetic counseling is strongly recommended to fully understand the implications of your test results.

Test Pricing and Details

Test Component Details
Test Name PITX3 Gene Anterior Segment Mesenchymal Dysgenesis NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next Generation Sequencing (NGS) Technology

Pre-Test Requirements

Before scheduling your test, please ensure:

  • Complete clinical history of the patient
  • Genetic counseling session to create detailed family pedigree chart
  • Documentation of affected family members with PITX3-related conditions
  • Review of previous ophthalmological evaluations and findings

Nationwide Availability

We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, and Philadelphia. Our network of certified genetic testing facilities ensures accessible, high-quality testing services nationwide.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic eye conditions affect your family’s future. Our PITX3 genetic test provides the answers you need for informed medical decisions and comprehensive care planning. With our discounted price of $500 USD (regularly $700 USD), advanced genetic testing is more accessible than ever.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take control of your genetic health journey.

Our team of genetic specialists and ophthalmologists are ready to provide comprehensive support throughout your testing process, from initial consultation to result interpretation and follow-up care planning.