Find Clarity About Spinal Muscular Atrophy in Your Family
When spinal muscular atrophy runs in your family, the uncertainty can feel overwhelming. We understand the mix of concern, questions, and hope that brings you here today. Our PLEKHG5 Gene Spinal Muscular Atrophy Distal Autosomal Recessive Type 4 NGS Genetic DNA Test provides the answers you need to move forward with confidence and peace of mind.
Understanding Your PLEKHG5 Genetic Test
This advanced Next-Generation Sequencing (NGS) test specifically examines the PLEKHG5 gene for mutations that cause distal spinal muscular atrophy type 4. Unlike traditional methods, NGS technology provides comprehensive analysis with exceptional accuracy, giving you reliable results you can trust for making important health decisions.
Spinal muscular atrophy type 4 is an autosomal recessive condition, meaning both parents must carry the gene mutation for a child to be affected. Our test helps identify carriers and affected individuals, providing crucial information for family planning and proactive health management.
Who Should Consider This Genetic Test?
This test is particularly important if you or your family members experience:
- Progressive muscle weakness in hands and feet
- Difficulty with fine motor skills
- Family history of spinal muscular atrophy
- Planning pregnancy with known family genetic risks
- Unexplained muscle weakness or wasting
- Concerns about passing genetic conditions to children
Many South African families find reassurance through genetic testing, especially when there’s a known family history of neuromuscular conditions.
Why This Test Matters for Your Family’s Health
Early detection through genetic testing provides numerous benefits:
- Peace of Mind: Reduce uncertainty about genetic risks
- Informed Family Planning: Make confident decisions about having children
- Proactive Health Management: Early intervention opportunities
- Genetic Counselling Support: Professional guidance for your unique situation
- Family Awareness: Help relatives understand their potential risks
Understanding Your Test Results
We know waiting for genetic results can be anxiety-provoking. That’s why we provide:
- Clear, Understandable Reports: Written in plain language with medical support
- Genetic Counselling Session: Included to help interpret your results
- Family Pedigree Analysis: Visual mapping of family genetic patterns
- Follow-up Guidance: Next steps based on your specific results
- Confidential Support: Your privacy is always protected
Whether your results show no mutations, carrier status, or affected status, we provide the support and guidance you need to understand what it means for your health journey.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price |
|---|---|---|
| PLEKHG5 Genetic Test | ZAR 9,350 | ZAR 6,700 |
| Genetic Counselling Session | INCLUDED | |
| Family Pedigree Analysis | INCLUDED | |
| Results Interpretation | INCLUDED | |
Turnaround Time: 3-4 weeks
Sample Type: Blood, Extracted DNA, or One drop Blood on FTA Card
Why Trust Oracle Genomics?
We’ve helped thousands of South African families navigate genetic health concerns with:
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Medical Expertise: Specialist neurologist oversight
- Advanced Technology: Latest NGS testing methods
- Patient-Centred Care: Empathetic support throughout your journey
- Proven Accuracy: Reliable results you can trust
- Confidential Service: Your privacy is our priority
Take the First Step Toward Genetic Clarity
Don’t let uncertainty about spinal muscular atrophy control your family’s future. Our comprehensive testing and counselling provide the answers and support you need.
Every day you wait is another day of uncertainty. Take control of your genetic health story today with testing you can trust.
