Sale!

SPTLC2 Gene Neuropathy Hereditary Sensory and Autonomic Type 1C NGS Genetic DNA Test

Original price was: R9,350.Current price is: R6,700.

-28%

Living with unexplained numbness, tingling, or pain in your hands and feet can be frightening and isolating. Our SPTLC2 Gene Neuropathy DNA test provides the answers you need to understand your hereditary sensory and autonomic neuropathy type 1C risk. For only ZAR 6,700 (regularly ZAR 9,350), this comprehensive NGS genetic test offers life-changing clarity about your neurological health. We understand the anxiety that comes with unexplained symptoms, which is why our test includes professional genetic counselling to help you understand your family history and results. With results available in just 3-4 weeks and nationwide coverage across South Africa, you can take control of your health journey with confidence and peace of mind. Our advanced testing technology ensures the highest accuracy, giving you reliable information to make informed healthcare decisions for yourself and your family.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

SPTLC2 Neuropathy DNA Test | ZAR 6
SPTLC2 Gene Neuropathy Hereditary Sensory and Autonomic Type 1C NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Find Clarity About Your Neurological Health with SPTLC2 Gene Testing

When unexplained numbness, burning sensations, or loss of feeling in your hands and feet disrupt your daily life, it’s natural to feel anxious and uncertain. You deserve answers about what’s causing these distressing symptoms. Our SPTLC2 Gene Neuropathy DNA test provides the definitive clarity you need to understand hereditary sensory and autonomic neuropathy type 1C – a condition that affects how your nerves communicate pain, temperature, and touch sensations.

Understanding Your SPTLC2 Neuropathy Test

This advanced genetic test examines the SPTLC2 gene, which plays a crucial role in maintaining healthy nerve function. When this gene has specific changes, it can lead to hereditary sensory and autonomic neuropathy type 1C – a condition that gradually affects your ability to feel pain, temperature, and touch. Our Next Generation Sequencing (NGS) technology provides the most comprehensive analysis available, giving you and your healthcare provider precise information about your genetic risk.

We understand that genetic testing can feel overwhelming, which is why we include professional genetic counselling as part of your testing journey. This ensures you fully understand what the test involves and what your results mean for your health.

Who Should Consider This Important Test?

This test is particularly important if you experience:

  • Unexplained numbness or tingling in your hands and feet
  • Burning pain or unusual sensations in your limbs
  • Difficulty sensing temperature changes or pain
  • Family history of similar neurological symptoms
  • Progressive loss of sensation that worries you
  • Foot injuries or ulcers that develop without pain awareness

If these symptoms sound familiar, or if neuropathy runs in your family, this test could provide the answers you’ve been seeking to manage your health proactively.

Why Early Detection Matters for Your Health

Getting tested for SPTLC2 gene neuropathy offers significant benefits for your long-term wellbeing:

  • Peace of Mind: Replace uncertainty with clear understanding of your condition
  • Early Intervention: Begin appropriate management strategies before symptoms progress
  • Family Planning: Understand inheritance patterns for future family decisions
  • Personalised Care: Work with your neurologist to create a targeted treatment plan
  • Prevent Complications: Reduce risk of injuries and other neuropathy-related issues

Many patients tell us that getting their results was the turning point in taking control of their health journey.

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. Our team ensures you receive clear, compassionate guidance throughout the process:

  • Comprehensive Report: Easy-to-understand results with detailed explanations
  • Genetic Counselling: Professional support to interpret your results
  • Next Steps Guidance: Clear recommendations for follow-up care
  • Family Implications: Understanding what results mean for relatives

Your results will clearly indicate whether SPTLC2 gene changes were detected and what this means for your neurological health management.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
SPTLC2 Gene Neuropathy DNA Test ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive genetic analysis, professional genetic counselling session, detailed results report, and ongoing support from our medical team.

Consider this: Early detection could save you from years of uncertainty and potentially prevent costly complications down the line.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS testing for maximum accuracy
  • Quick Turnaround: Results typically available within 3-4 weeks
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Complete Preparation Support: We guide you through clinical history documentation and family pedigree creation

Take the First Step Toward Clarity Today

Don’t let uncertainty about your neurological symptoms control your life. Every day you wait is another day without answers. Our team is ready to support you through this important health journey with compassion and expertise.



Limited Time Offer: Secure your special pricing of ZAR 6,700 before this opportunity ends. Take control of your health story today.