Understanding Hyperlysinemia Type 1: Your Path to Genetic Clarity
When developmental concerns or metabolic symptoms appear in your family, the uncertainty can be overwhelming. You deserve clear answers and a compassionate approach to genetic testing. Our AASS Gene Hyperlysinemia Type 1 NGS Genetic DNA Test provides the definitive clarity you need to make informed health decisions for yourself and your loved ones.
What This Test Reveals About Your Health
Hyperlysinemia Type 1 is a rare metabolic disorder caused by mutations in the AASS gene, which affects how your body processes the amino acid lysine. Our advanced Next-Generation Sequencing (NGS) technology examines your DNA with exceptional precision, identifying even the smallest genetic variations that could impact your health. This isn’t just a test – it’s a comprehensive health assessment that gives you and your healthcare provider the information needed for proactive care.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Unexplained developmental delays in children
- Muscle weakness or coordination difficulties
- Family history of metabolic disorders
- Seizures or neurological symptoms without clear cause
- Previous inconclusive metabolic testing results
- Planning for pregnancy with family history concerns
Many South African families find peace of mind through early detection, allowing for better management and treatment planning.
Why Early Detection Matters for Your Family’s Health
Getting tested for Hyperlysinemia Type 1 provides crucial benefits:
- Early Intervention: Identify risks before symptoms become severe
- Family Planning: Make informed decisions about future pregnancies
- Treatment Guidance: Work with your doctor on targeted management strategies
- Peace of Mind: Reduce uncertainty and anxiety about genetic risks
- Proactive Health: Take control of your family’s health journey
Understanding Your Test Results with Compassion
We understand that waiting for genetic test results can be stressful. That’s why we provide:
- Clear Explanations: Your results come with easy-to-understand interpretations
- Genetic Counselling: Included session to discuss findings and next steps
- Family Pedigree Analysis: Visual mapping of family health patterns
- Medical Guidance: Recommendations for follow-up with your healthcare provider
- Ongoing Support: Our team is here to answer your questions
Whether your results show typical genetic patterns or identify variations, you’ll have the support and information needed to move forward confidently.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| AASS Gene Hyperlysinemia Type 1 NGS Test | ZAR 6,700 | |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Turnaround Time: 3-4 weeks
Sample Type: Blood sample
Preparation: Clinical history and genetic counselling session required
Why South Africans Trust Oracle Genomics
We’ve built our reputation on accuracy, compassion, and accessibility:
- Nationwide Coverage: Convenient testing locations in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Tests supervised by qualified general physicians and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for unmatched accuracy
- Patient Privacy: Strict confidentiality and data protection protocols
- Proven Track Record: Thousands of South African families served with care
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty about genetic risks affect your family’s future. Our compassionate team is ready to guide you through the testing process with the expertise and care you deserve.
Limited Time Offer: Save ZAR 2,650 on comprehensive Hyperlysinemia Type 1 testing with included genetic counselling. Early detection could make all the difference for your family’s health journey.
“The clarity we gained from this test helped our family make informed decisions and reduced our anxiety significantly. The genetic counselling was invaluable.” – Satisfied Oracle Genomics Patient
