PAX2 Gene Papillorenal Syndrome NGS Genetic DNA Test
Comprehensive Genetic Analysis for Kidney and Eye Health
The PAX2 Gene Papillorenal Syndrome NGS Genetic DNA Test represents a breakthrough in genetic diagnostics, offering precise detection of mutations associated with Papillorenal Syndrome. This condition, also known as renal-coloboma syndrome, affects multiple organ systems and requires early intervention for optimal management outcomes.
What Does This Test Measure?
This advanced genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the PAX2 gene for specific mutations linked to Papillorenal Syndrome. The test examines:
- Complete sequencing of the PAX2 gene coding regions
- Detection of point mutations, insertions, and deletions
- Identification of genetic variants affecting kidney and eye development
- Assessment of inheritance patterns for family planning
Who Should Consider This Test?
This genetic screening is recommended for individuals experiencing:
- Unexplained kidney abnormalities or renal insufficiency
- Congenital eye defects, particularly optic nerve colobomas
- Hearing loss or auditory processing difficulties
- Family history of Papillorenal Syndrome or related conditions
- Children with developmental delays affecting multiple systems
- Individuals with dysmorphic features suggesting genetic syndromes
Key Benefits of PAX2 Genetic Testing
- Early Intervention: Enables proactive management of kidney and eye complications
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Personalized Care: Guides targeted monitoring and treatment strategies
- Peace of Mind: Offers clarity for families with hereditary conditions
- Comprehensive Analysis: Utilizes cutting-edge NGS technology for accurate results
Understanding Your Test Results
Your genetic test results will be thoroughly explained by our certified genetic counselors:
- Positive Result: Indicates the presence of PAX2 gene mutation, confirming Papillorenal Syndrome diagnosis
- Negative Result: Suggests absence of known PAX2 mutations, though clinical follow-up may still be recommended
- Variant of Uncertain Significance: Identifies genetic changes requiring additional research and monitoring
All results include detailed interpretation and recommendations for next steps in medical management.
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Centers
We have conveniently located branches across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality genetic testing services nationwide.
Pre-Test Requirements
Before scheduling your PAX2 Gene Papillorenal Syndrome test, please ensure:
- Complete clinical history documentation
- Genetic counseling session to create family pedigree chart
- Discussion of testing implications with healthcare provider
- Understanding of potential outcomes and next steps
Sample Collection and Processing
We accept multiple sample types for your convenience:
- Blood samples collected by certified phlebotomists
- Extracted DNA from previous genetic testing
- One drop of blood on FTA card for easy transport
Results are typically available within 3 to 4 weeks from sample receipt.
Take Control of Your Genetic Health Today
Don’t wait to get the answers you need about potential genetic conditions affecting kidney and eye health. Our expert team of genetic counselors and medical professionals is ready to guide you through the testing process and provide comprehensive support.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your PAX2 Gene Papillorenal Syndrome NGS Genetic DNA Test and take the first step toward understanding your genetic health.
