Find Clarity About Tyrosinemia Type 2 Genetic Risks
When you’re worried about inherited health conditions affecting your family, the uncertainty can be overwhelming. Our TAT Gene Tyrosinemia Type 2 NGS Genetic DNA Test provides the definitive answers you need to protect your family’s future health. Using cutting-edge next-generation sequencing technology, we deliver accurate, reliable results that empower you to make informed decisions.
Understanding Your Tyrosinemia Type 2 Genetic Test
Tyrosinemia Type 2 is a rare inherited disorder caused by mutations in the TAT gene, which affects how your body processes the amino acid tyrosine. Our advanced NGS (Next-Generation Sequencing) technology examines your DNA to identify these specific genetic variations with exceptional precision. Unlike basic genetic tests, NGS provides comprehensive analysis of the entire TAT gene, ensuring no mutation goes undetected.
The test requires either a blood sample, extracted DNA, or a simple blood spot on an FTA card, making the process convenient and accessible for patients across South Africa.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Unexplained eye problems or painful eye lesions
- Developmental delays in childhood
- Intellectual disability without clear cause
- Skin lesions on palms and soles
- Family history of similar symptoms
- Planning pregnancy with known family risk factors
If you’re experiencing any of these symptoms or have concerns about inherited conditions in your family, this test can provide the clarity you need.
Why Early Detection Matters for Your Health
Identifying Tyrosinemia Type 2 early can significantly improve health outcomes and quality of life. With accurate genetic information, you can:
- Implement appropriate dietary management strategies
- Prevent serious complications before they develop
- Make informed family planning decisions
- Access targeted treatments and monitoring
- Reduce anxiety through definitive diagnosis
- Create a proactive health management plan
Early intervention can prevent the progressive damage that untreated Tyrosinemia Type 2 can cause to multiple organ systems.
Understanding Your Test Results
We understand that waiting for genetic test results can be stressful. That’s why we provide comprehensive support throughout the process. Your results will clearly indicate:
- Presence or absence of TAT gene mutations
- Specific genetic variations identified
- Interpretation of what the results mean for your health
- Recommendations for next steps and management
Our genetic counselling session included with your test ensures you fully understand your results and their implications for you and your family.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| TAT Gene Tyrosinemia Type 2 NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
Your investment includes: Comprehensive NGS genetic analysis, professional genetic counselling session, detailed pedigree chart creation, and complete results interpretation.
Why Trust Oracle Genomics?
We’re committed to providing South Africans with accessible, reliable genetic testing services:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified general physicians
- Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
- Genetic Counselling: Professional support included with every test
- Proven Track Record: Trusted by healthcare professionals nationwide
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic risks affect your peace of mind. Early detection through genetic testing can provide the answers you need to protect your family’s health future.
Test Details:
- Turnaround Time: 3-4 weeks
- Sample Type: Blood, Extracted DNA, or Blood on FTA Card
- Preparation: Clinical history and genetic counselling session
- Method: Advanced NGS Technology
