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CLN3 Gene Ceroid Lipofuscinosis Neuronal Type 3 NGS Genetic DNA Test

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

-28%

Facing concerns about Batten disease in your family? Our CLN3 Gene Ceroid Lipofuscinosis Neuronal Type 3 NGS Genetic DNA Test provides the clarity you need for ZAR 6,700. This comprehensive test uses advanced Next Generation Sequencing technology to detect mutations in the CLN3 gene, which causes Batten disease – a rare but serious neurological condition. Early detection can help you make informed decisions about family planning and medical management. With results in just 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, we make genetic testing accessible and reliable. Our process includes professional genetic counselling to ensure you understand your results and their implications. Take control of your family’s health journey with confidence and accuracy.

📞 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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CLN3 Gene Test ZAR 6
CLN3 Gene Ceroid Lipofuscinosis Neuronal Type 3 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Batten Disease with Our CLN3 Gene Test

When neurological conditions run in families, the uncertainty can be overwhelming. Our CLN3 Gene Ceroid Lipofuscinosis Neuronal Type 3 NGS Genetic DNA Test provides the answers you need to make informed decisions about your family’s health future. For just ZAR 6,700, gain peace of mind through advanced genetic testing available nationwide.

Understanding the CLN3 Gene Test

The CLN3 gene test examines your DNA for mutations that cause Batten disease, also known as neuronal ceroid lipofuscinosis type 3. This progressive neurological disorder typically begins in childhood and affects vision, motor skills, and cognitive function. Our test uses Next Generation Sequencing (NGS) technology, the gold standard in genetic analysis, to provide highly accurate results you can trust.

Unlike basic genetic tests, our comprehensive approach examines the entire CLN3 gene, ensuring no mutation goes undetected. This thorough analysis gives you and your healthcare provider the complete picture needed for proper diagnosis and management.

Who Should Consider This Test?

This test is particularly important if you or your child experience:

  • Progressive vision loss starting in childhood
  • Developmental delays or regression in motor skills
  • Seizures or epilepsy that began in early childhood
  • Speech difficulties or cognitive decline
  • Family history of Batten disease or similar neurological conditions

If you’re planning a family and have relatives affected by Batten disease, this test can provide crucial information for family planning decisions.

Why Early Detection Matters for Your Family’s Health

Early diagnosis of Batten disease through genetic testing offers significant benefits:

  • Informed Medical Management: Early intervention can help manage symptoms and improve quality of life
  • Family Planning Confidence: Understand inheritance patterns to make informed reproductive decisions
  • Reduced Diagnostic Uncertainty: End the diagnostic odyssey and get clear answers
  • Access to Support Services: Connect with appropriate medical specialists and support networks
  • Peace of Mind: Replace uncertainty with knowledge and a clear path forward

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. Our process is designed to provide clarity and support:

Positive Result: If a CLN3 mutation is detected, our genetic counsellors will explain what this means for you and your family, discuss management options, and connect you with appropriate specialists.

Negative Result: If no mutations are found, this can provide significant relief and help rule out Batten disease as a cause of symptoms.

Variant of Uncertain Significance: Sometimes, we find genetic changes whose significance isn’t yet known. In these cases, we’ll provide ongoing monitoring and updates as research advances.

Every result includes a comprehensive consultation with our genetic counselling team to ensure you fully understand the implications.

Transparent Pricing – No Hidden Costs

Service Regular Price Special Price
CLN3 Gene Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session Included
Family Pedigree Analysis Included
Results Consultation Included

Our special pricing represents excellent value compared to the potential lifelong costs of undiagnosed neurological conditions.

Why Trust Oracle Genomics?

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

  • Nationwide Coverage: Serving patients in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Advanced Technology: Using NGS technology for the most accurate genetic analysis available
  • Expert Team: Board-certified genetic counsellors and medical professionals
  • Comprehensive Support: From initial consultation through results explanation
  • Proven Accuracy: Rigorous quality control ensures reliable results

Simple Testing Process

  1. Genetic Counselling: Initial session to understand your family history and create a pedigree chart
  2. Sample Collection: Simple blood draw or FTA card sample at our nationwide facilities
  3. Advanced Analysis: NGS technology examination in our accredited laboratory
  4. Results Delivery: Comprehensive report within 3-4 weeks
  5. Results Consultation: Detailed explanation with our genetic counselling team

Take the First Step Toward Clarity

Don’t let uncertainty about Batten disease control your family’s future. With our CLN3 gene test, you can:

  • Get definitive answers about genetic risks
  • Make informed family planning decisions
  • Access appropriate medical care and support
  • Gain peace of mind for your family’s health journey

Book your genetic counselling session today and take control of your family’s genetic health. Our team is ready to support you through every step of this important journey.


Limited time special pricing available. Early detection can make all the difference in managing neurological conditions.