Understanding Juvenile Primary Lateral Sclerosis: Your Family’s Neurological Health Matters
When neurological symptoms appear in children or young adults, the uncertainty can be overwhelming. Our ALS2 gene test provides the clarity and answers your family deserves. Using cutting-edge NGS technology, we deliver accurate results that can guide treatment decisions and provide peace of mind.
What This Test Reveals About Your Genetic Health
The ALS2 gene test specifically analyses mutations associated with juvenile primary lateral sclerosis (PLS), a rare neurological condition that affects motor neurons. Unlike standard genetic tests, our NGS technology examines the entire ALS2 gene with exceptional precision, identifying even subtle genetic variations that could impact your family’s neurological health.
This isn’t just a test – it’s a comprehensive genetic assessment that considers your family history through professional genetic counselling, ensuring we understand your unique genetic landscape.
Is This Test Right for Your Family?
Consider this essential genetic testing if your family experiences:
- Progressive muscle weakness or stiffness in children or young adults
- Family history of neurological disorders, particularly PLS or ALS
- Difficulty with coordination, balance, or fine motor skills in youth
- Speech difficulties or swallowing problems developing in childhood
- Unexplained muscle spasms or cramping in family members
- Concerns about passing neurological conditions to future generations
Early genetic insight can transform how you approach neurological health management for your entire family.
Why Early Genetic Detection Changes Everything
Knowing your ALS2 gene status provides more than just information – it provides power:
- Proactive Healthcare: Early detection allows for timely interventions and management strategies
- Family Planning Confidence: Understand genetic risks for future generations
- Treatment Guidance: Results can inform targeted therapeutic approaches
- Emotional Peace: Replace uncertainty with clear, actionable information
- Cost Savings: Early intervention often reduces long-term healthcare expenses
Understanding Your Results: Clear, Compassionate Guidance
We know genetic results can feel overwhelming. That’s why our process includes:
- Comprehensive Genetic Counselling: Before testing, we help map your family history
- Clear Result Interpretation: Our neurologists explain findings in understandable terms
- Personalised Next Steps: We provide specific recommendations based on your results
- Ongoing Support: Access to neurological specialists for follow-up care
Whether results are positive or negative, you’ll leave with a clear understanding and actionable plan.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| ALS2 Gene NGS Test | ZAR 9,350 | ZAR 6,700 | ZAR 2,650 |
| Genetic Counselling Session | INCLUDED | ||
| Family Pedigree Analysis | INCLUDED | ||
| Neurologist Consultation | INCLUDED | ||
This comprehensive package represents exceptional value compared to piecemeal neurological genetic testing.
Why South Africans Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS sequencing for 99.9% accuracy
- Quick Turnaround: Results in just 3-4 weeks, not months
- Multiple Sample Options: Blood, extracted DNA, or simple FTA card blood drop
- Comprehensive Support: From initial counselling to result interpretation
Take Control of Your Family’s Neurological Health Today
Don’t let uncertainty about genetic neurological conditions create unnecessary stress. Early detection through our ALS2 gene test can provide the answers and peace of mind your family deserves.
Limited Time Special: Book now to secure the ZAR 6,700 special price before it returns to ZAR 9,350. Your family’s neurological health is worth this investment in certainty.
“Early genetic detection transformed our family’s approach to neurological health. The clarity we gained was priceless.” – Recent Oracle Genomics Patient
