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CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 NGS Genetic DNA Test

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

-28%

Facing concerns about Neuronal Ceroid Lipofuscinosis? Our CLN6 Gene Test provides definitive answers through advanced NGS technology. For only ZAR 6,700 (regularly ZAR 9,350), this comprehensive genetic analysis detects mutations in the CLN6 gene, helping families understand their risk and plan for the future. Early detection is crucial for managing this rare neurological condition, and our test offers 99.9% accuracy with results in just 3-4 weeks. Available nationwide across South Africa, including Johannesburg, Cape Town, and Durban, we provide compassionate genetic counselling to guide you through the process. Take control of your family’s health journey with confidence and clarity.

📞 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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CLN6 Gene Test ZAR 6
CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding CLN6 Gene Testing: Your Path to Clarity About Neuronal Ceroid Lipofuscinosis

When neurological symptoms appear in your family, the uncertainty can be overwhelming. Our CLN6 Gene Test provides the answers you need to understand Neuronal Ceroid Lipofuscinosis Type 6, a rare but serious inherited condition. We’re here to guide you with compassion and medical expertise, helping South African families navigate complex genetic health concerns.

What Does the CLN6 Gene Test Detect?

This advanced Next-Generation Sequencing (NGS) test specifically analyses the CLN6 gene for mutations that cause Neuronal Ceroid Lipofuscinosis Type 6. This condition affects the nervous system and can lead to progressive neurological decline. By identifying specific genetic changes, we help families understand their risk and make informed healthcare decisions.

Our test examines the entire CLN6 gene sequence with exceptional accuracy, detecting even subtle mutations that might be missed by conventional testing methods.

Who Should Consider This Genetic Test?

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

  • Progressive vision loss or retinal degeneration
  • Seizures or epilepsy that begins in childhood
  • Developmental regression or loss of motor skills
  • Cognitive decline or dementia symptoms
  • Family history of similar neurological conditions
  • Unexplained neurological symptoms in multiple family members

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

Why Early Detection Matters for Your Family’s Health

Getting tested for CLN6 mutations offers significant benefits:

  • Peace of Mind: Eliminate uncertainty about your genetic risk
  • Early Intervention: Access appropriate care and management strategies sooner
  • Family Planning: Make informed decisions about having children
  • Treatment Guidance: Help healthcare providers develop targeted care plans
  • Genetic Counselling: Understand inheritance patterns and family risks

Early detection can significantly improve quality of life and help families prepare for future healthcare needs.

Understanding Your Test Results

We know waiting for genetic test results can be stressful. Our team provides clear, compassionate explanations of your results:

  • Positive Result: Indicates a CLN6 gene mutation is present. Our genetic counsellors will explain what this means for you and your family, discussing management options and next steps.
  • Negative Result: No CLN6 mutations were detected. This significantly reduces the likelihood of Neuronal Ceroid Lipofuscinosis Type 6 in your family.
  • Uncertain Variant: Sometimes we find genetic changes with unknown significance. We’ll explain these findings and recommend appropriate follow-up.

All results come with comprehensive genetic counselling to ensure you fully understand the implications for your health and family.

Transparent Pricing – Special Offer for South African Families

Test Description Regular Price Special Price Turnaround Time
CLN6 Gene Ceroid Lipofuscinosis Neuronal Type 6 NGS Test ZAR 9,350 ZAR 6,700 3-4 Weeks

Sample Requirements: Blood, Extracted DNA, or One Drop of Blood on FTA Card

Preparation Needed: Clinical history and genetic counselling session to create a family pedigree chart

Considering the potential healthcare costs of undiagnosed neurological conditions, this test represents excellent value for your family’s long-term health planning.

Why Trust Oracle Genomics?

We’re committed to providing South African families with world-class genetic testing services:

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified General Physicians
  • Advanced Technology: Using cutting-edge NGS technology for maximum accuracy
  • Compassionate Care: Genetic counselling included with every test
  • Proven Accuracy: 99.9% detection rate for CLN6 gene mutations

We understand the emotional journey of genetic testing and provide support every step of the way.

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about Neuronal Ceroid Lipofuscinosis control your family’s future. Early detection through genetic testing can provide the answers you need to make informed healthcare decisions.

Limited Time Offer: This special pricing of ZAR 6,700 (save ZAR 2,650) won’t last forever. Book your test today to secure this valuable health investment for your family.

Available at medical centres throughout South Africa, including major cities and regional areas. Your journey to genetic clarity starts with one simple test.