Sale!

KANSL1 Gene Koolen Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about developmental delays or intellectual disabilities in your child? The KANSL1 Gene Koolen Syndrome NGS Genetic DNA Test provides definitive answers and peace of mind for South African families. This advanced genetic test uses Next Generation Sequencing technology to accurately detect mutations in the KANSL1 gene, which is responsible for Koolen-de Vries syndrome. For only ZAR 6,700 (regularly ZAR 9,350), you gain access to professional genetic counselling and comprehensive analysis that can guide your family’s healthcare decisions. Early detection through this test allows for better management of developmental challenges and helps create appropriate support strategies. Our nationwide coverage ensures accessibility for families across South Africa, from Johannesburg to Cape Town and Durban. Trust Oracle Genomics for accurate, reliable genetic testing that puts your family’s health first with results delivered within 3-4 weeks.

📞 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

KANSL1 Gene Koolen Syndrome DNA Test | ZAR 6
KANSL1 Gene Koolen Syndrome 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”]

Understanding KANSL1 Gene Koolen Syndrome: Your Path to Clarity and Peace of Mind

When you notice developmental delays or intellectual challenges in your child, the uncertainty can be overwhelming. As parents, you deserve clear answers and a roadmap for your child’s future. The KANSL1 Gene Koolen Syndrome NGS Genetic DNA Test provides the definitive clarity South African families need to make informed healthcare decisions and access the right support systems.

What This Test Reveals About Your Child’s Health

The KANSL1 Gene Koolen Syndrome test uses advanced Next Generation Sequencing (NGS) technology to examine the KANSL1 gene for mutations that cause Koolen-de Vries syndrome. This comprehensive analysis goes beyond surface-level observations to provide genetic confirmation, helping you understand the root cause of developmental concerns rather than just managing symptoms.

Our testing process begins with professional genetic counselling where we create a detailed family pedigree chart, ensuring we understand your complete family health history. This personalised approach means we’re not just running a test – we’re building a comprehensive picture of your child’s genetic health.

Is This Test Right for Your Family?

This genetic test is particularly important for families who have noticed:

  • Unexplained developmental delays in motor skills or speech
  • Intellectual disability or learning challenges
  • Distinctive facial features that may suggest genetic conditions
  • Family history of similar developmental patterns
  • Concerns about your child’s growth and cognitive development

Many South African parents find relief in having concrete answers rather than living with uncertainty about their child’s developmental journey.

Why Early Detection Matters for Your Child’s Future

Getting a definitive diagnosis through genetic testing provides numerous benefits for your family’s wellbeing:

  • Personalised Care Planning: Understand exactly what support and interventions your child needs
  • Reduced Anxiety: Replace uncertainty with a clear understanding of your child’s condition
  • Early Intervention: Access appropriate therapies and educational support sooner
  • Family Planning Insights: Understand genetic risks for future pregnancies
  • Community Connection: Connect with other families facing similar challenges

Early detection means your child can receive targeted support during crucial developmental years, potentially improving long-term outcomes.

Understanding Your Results: Clear Guidance Every Step

We understand that genetic test results can feel overwhelming. That’s why our process includes comprehensive result interpretation and ongoing support:

  • Clear, easy-to-understand reports with plain language explanations
  • Professional guidance on what your results mean for your child’s health
  • Recommendations for next steps and appropriate healthcare providers
  • Ongoing access to genetic counselling for additional questions
  • Connection to relevant support networks and resources in South Africa

Your results will be ready within 3-4 weeks, and we’ll guide you through every detail to ensure you feel confident and supported.

Transparent Pricing for Peace of Mind

Service Regular Price Special Price Savings
KANSL1 Gene Koolen Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included: Comprehensive genetic analysis, professional genetic counselling session, detailed family pedigree chart, complete result interpretation, and ongoing support.

Sample Collection: Simple blood draw, extracted DNA, or one drop of blood on FTA card – we make the process comfortable for your child.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Advanced Technology: State-of-the-art NGS technology for maximum accuracy
  • Expert Team: Qualified genetic counsellors and medical professionals
  • Proven Accuracy: Reliable results you can trust for important healthcare decisions
  • Patient-First Approach: Empathetic support throughout your testing journey

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s development create unnecessary stress. The answers you need are within reach, and early detection can make a significant difference in your child’s quality of life.

Limited Time Offer: Save ZAR 2,650 on comprehensive KANSL1 genetic testing. Take advantage of this special pricing while available.

Convenient Nationwide Access: With testing locations across South Africa, getting the answers you need has never been easier. From major cities to regional centres, we’re here to support your family’s health journey.