Find Clarity About Tyrosinemia Type 1B Genetic Risks
When metabolic disorders run in your family, the uncertainty can be overwhelming. Our GSTZ1 Gene Tyrosinemia Type 1B test provides the definitive answers you need to protect your family’s health. Using cutting-edge NGS technology, we deliver 99.9% accurate results that empower you to make informed healthcare decisions.
Understanding Your GSTZ1 Gene Test
Tyrosinemia Type 1B is a rare inherited metabolic disorder caused by mutations in the GSTZ1 gene. This condition affects how your body processes the amino acid tyrosine, potentially leading to serious liver and kidney complications if undetected. Our Next-Generation Sequencing (NGS) technology examines your GSTZ1 gene with precision, identifying even the smallest genetic variations that could impact your health.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Unexplained liver problems or elevated liver enzymes
- Family history of metabolic disorders
- Infants with feeding difficulties or failure to thrive
- Previous children diagnosed with Tyrosinemia
- Planning pregnancy with known family genetic risks
Early detection through genetic testing can prevent serious complications and guide appropriate treatment strategies.
Why This Test Matters for Your Family’s Health
Getting tested provides invaluable benefits:
- Peace of Mind: Eliminate uncertainty about genetic risks
- Early Intervention: Detect conditions before symptoms appear
- Family Planning: Make informed decisions about having children
- Personalized Care: Guide medical management based on your genetic profile
- Prevention: Implement lifestyle changes to minimize risks
Understanding Your Test Results
We make understanding your results straightforward and reassuring. Our genetic counsellors will:
- Explain your results in clear, simple language
- Discuss what the findings mean for your health
- Provide guidance on next steps and medical management
- Help you understand implications for family members
- Connect you with appropriate specialists if needed
Remember: A positive result doesn’t mean you’ll definitely develop symptoms, but it does provide valuable information for proactive health management.
Affordable Genetic Testing for South Africans
| Service | Regular Price | Special Price |
|---|---|---|
| GSTZ1 Gene Tyrosinemia Type 1B NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Interpretation | Included | |
Turnaround time: 3-4 weeks | Sample: Blood, DNA, or FTA Card
Why Trust Oracle Genomics?
We’re committed to providing South Africans with accessible, reliable genetic testing:
- Nationwide Coverage: Testing available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Our tests are supervised by qualified general physicians
- Advanced Technology: NGS technology ensures highest accuracy standards
- Patient-Focused: Genetic counselling included with every test
- Confidential: Your genetic information is protected with strict privacy protocols
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic risks affect your peace of mind. Our special pricing of ZAR 6,700 makes this crucial testing more accessible than ever.
Limited Time Offer: This special pricing won’t last forever. Secure your family’s health future while you can save ZAR 2,650.
Convenient Testing: Choose from blood draw, DNA sample, or simple FTA card option. We coordinate with local clinics nationwide.
