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TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive NGS Genetic DNA Test

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

-28%

Facing concerns about hereditary neurological conditions? Our TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy test provides definitive answers for South African families. Using advanced NGS technology, this comprehensive DNA analysis detects autosomal recessive mutations that cause progressive neurological deterioration. For just ZAR 6,700 (regularly ZAR 9,350), you gain access to precise genetic insights that can guide treatment decisions and family planning. Early detection is crucial for managing symptoms and improving quality of life. Our nationwide coverage ensures accessibility from Johannesburg to Cape Town, with results delivered in 3-4 weeks. Trust Oracle Genomics for accurate, confidential testing backed by neurological expertise and compassionate 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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TDP1 Gene Ataxia Test ZAR 6
TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy Autosomal Recessive NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Hereditary Neurological Conditions in South Africa

When neurological symptoms begin affecting your coordination, balance, or nerve function, the uncertainty can be overwhelming. Many South African families face the challenge of hereditary neurological conditions without clear answers. Our TDP1 Gene Spinocerebellar Ataxia with Axonal Neuropathy test provides the clarity you need to make informed health decisions for yourself and your family.

What This Test Detects

This advanced genetic test identifies mutations in the TDP1 gene responsible for autosomal recessive spinocerebellar ataxia with axonal neuropathy. Using Next Generation Sequencing (NGS) technology, we analyse your DNA to detect specific genetic variations that cause progressive neurological deterioration affecting both the cerebellum and peripheral nerves.

Who Should Consider This Test

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

  • Progressive difficulty with coordination and balance
  • Muscle weakness or numbness in limbs
  • Family history of similar neurological symptoms
  • Early-onset movement disorders
  • Concerns about passing genetic conditions to children

Why Early Detection Matters for Your Health

Identifying TDP1 gene mutations early provides significant benefits:

  • Enables proactive symptom management strategies
  • Informs family planning decisions
  • Provides clarity for unexplained neurological symptoms
  • Connects you with appropriate neurological specialists
  • Reduces diagnostic uncertainty and anxiety

Understanding Your Results

Our comprehensive report provides clear, actionable information about your genetic status. Positive results indicate the presence of TDP1 gene mutations, while negative results provide reassurance. All results include genetic counselling recommendations to help you understand the implications for your health and family.

Affordable Genetic Testing for South Africans

Test Option Price Turnaround
Regular Price ZAR 9,350 3-4 Weeks
Special Price ZAR 6,700 3-4 Weeks

Nationwide Accessibility

We provide testing services across South Africa, with convenient sample collection available in Johannesburg, Cape Town, Durban, Pretoria, and surrounding areas. Our network ensures you can access this important genetic testing regardless of your location.

Take Control of Your Neurological Health Today

Don’t let uncertainty about hereditary conditions affect your peace of mind. Our TDP1 gene testing provides the answers you need to make informed health decisions. With our special pricing of ZAR 6,700 and comprehensive genetic counselling support, you’re taking an important step toward understanding your neurological health.

Book your consultation today to discuss whether this test is right for you and your family. Early detection can make a significant difference in managing neurological conditions effectively.