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AP5Z1 Gene SPG48 NGS Genetic DNA Test

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

-28%

Facing concerns about hereditary spastic paraplegia or unexplained walking difficulties in your family? The AP5Z1 Gene SPG48 NGS Genetic DNA Test provides definitive answers about your genetic risk for this neurological condition. For only ZAR 6,700 (regularly ZAR 9,350), this advanced test uses Next Generation Sequencing technology to deliver 99.9% accurate results within 3-4 weeks. Our comprehensive approach includes professional genetic counselling to understand your family history and create a detailed pedigree chart. Early detection can help you make informed health decisions, access appropriate treatments, and provide peace of mind for your family’s future. Oracle Genomics brings this cutting-edge testing to major South African cities including Johannesburg, Cape Town, and Durban with the highest standards of medical accuracy and patient care.

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

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
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AP5Z1 SPG48 Genetic Test | ZAR 6
AP5Z1 Gene SPG48 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Genetic Risk for Hereditary Spastic Paraplegia

When walking difficulties, muscle stiffness, or neurological symptoms run in your family, the uncertainty can be overwhelming. The AP5Z1 Gene SPG48 NGS Genetic DNA Test provides the clarity you need to understand your genetic predisposition to hereditary spastic paraplegia. We understand the emotional weight of genetic concerns, which is why we’ve made this advanced testing accessible and affordable for South African families.

What Does the AP5Z1 SPG48 Test Detect?

This specialised genetic test examines the AP5Z1 gene for mutations associated with SPG48, a form of hereditary spastic paraplegia that affects nerve pathways controlling muscle movement in your legs. Using Next Generation Sequencing (NGS) technology, we analyse your DNA with exceptional precision to identify even the smallest genetic variations that could impact your neurological health.

Our testing process begins with comprehensive genetic counselling, where our specialists help you map your family’s health history to better understand your specific risk factors and testing needs.

Who Should Consider This Genetic Test?

This test is particularly important if you or your family members experience:

  • Progressive walking difficulties or gait abnormalities
  • Muscle stiffness and spasticity in the legs
  • Family history of neurological conditions
  • Unexplained balance problems or frequent falls
  • Early-onset mobility issues in multiple family members
  • Concerns about passing genetic conditions to children

If you’re planning a family and have concerns about hereditary neurological conditions, this test can provide valuable insights for your reproductive decisions.

Why Early Detection Matters for Your Health

Understanding your genetic status empowers you to take proactive steps for your neurological health. Early detection through genetic testing can:

  • Provide clarity and reduce uncertainty about your health future
  • Enable early intervention and appropriate management strategies
  • Help you make informed family planning decisions
  • Connect you with specialist care and support resources
  • Reduce anxiety through definitive answers
  • Potentially slow disease progression through early management

Many patients report significant emotional relief after receiving their results, regardless of the outcome, because knowledge brings power and control.

Understanding Your Test Results

We know waiting for genetic results can be stressful. That’s why we provide clear, compassionate explanations of your findings:

  • Positive Result: Indicates an AP5Z1 gene mutation associated with SPG48. Our genetic counsellors will explain what this means for your health and connect you with appropriate neurological specialists.
  • Negative Result: No mutation detected in the AP5Z1 gene. This significantly reduces your risk of developing SPG48-related symptoms.
  • Variant of Uncertain Significance: Rarely, we may find a genetic change whose significance isn’t fully understood. We’ll monitor research and update you as new information emerges.

Our genetic counselling team ensures you fully understand your results and their implications for your health and family.

Transparent Pricing & Value

Service Regular Price Special Price Savings
AP5Z1 SPG48 NGS Genetic Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Genetic Counselling Session Included at no extra cost
Family Pedigree Analysis Included in package

This comprehensive package represents exceptional value compared to international testing costs, making advanced genetic care accessible to South African families.

Why Trust Oracle Genomics?

We’ve built our reputation on accuracy, compassion, and accessibility:

  • Nationwide Coverage: Serving patients 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 technology for 99.9% accuracy
  • Quick Turnaround: Results typically within 3-4 weeks
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Comprehensive Support: From initial counselling through results interpretation

Take Control of Your Genetic Health Today

Don’t let uncertainty about hereditary spastic paraplegia control your future. Early detection through genetic testing can provide the answers you need to make informed health decisions.

Limited Time Offer: Book your AP5Z1 SPG48 genetic test at the special price of ZAR 6,700 (save ZAR 2,650) and receive comprehensive genetic counselling included.



Our team is ready to support you through every step of this important health journey. Contact us today to schedule your genetic counselling session and take the first step toward clarity and peace of mind.