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KDM6A Gene Kabuki Syndrome Type 2 NGS Genetic DNA Test

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

-28%

Facing concerns about developmental delays or unusual facial features in your child? Our KDM6A Gene Kabuki Syndrome Type 2 NGS Genetic DNA Test provides definitive answers and peace of mind for South African families. For only ZAR 6,700 (regularly ZAR 9,350), this advanced Next Generation Sequencing test delivers unparalleled accuracy in detecting mutations associated with Kabuki syndrome type 2. We understand the anxiety that comes with developmental concerns, which is why our comprehensive approach includes professional genetic counselling to help you understand your family’s genetic history. With results available within 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, you can trust Oracle Genomics for reliable, confidential genetic testing that puts your family’s health first. Early detection means earlier intervention and better outcomes for your child’s development.

📞 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

KDM6A Kabuki Syndrome DNA Test | ZAR 6
KDM6A Gene Kabuki Syndrome Type 2 NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Finding Answers for Your Child’s Development: KDM6A Kabuki Syndrome Genetic Testing

As a parent, watching your child struggle with developmental delays or unusual physical features can be heart-wrenching. You want answers, and you want them from a source you can trust. At Oracle Genomics, we understand the emotional journey you’re on, and we’re here to provide the clarity and guidance your family deserves.

Understanding the KDM6A Kabuki Syndrome Genetic Test

Kabuki syndrome type 2 is a rare genetic condition that affects multiple body systems, often presenting with distinctive facial features, developmental delays, and potential health complications. Our advanced NGS (Next Generation Sequencing) technology examines the KDM6A gene with exceptional precision, identifying mutations that could be responsible for your child’s symptoms.

This isn’t just another test – it’s a comprehensive diagnostic journey that includes professional genetic counselling to help you understand your family’s complete health picture.

Who Should Consider This Genetic Test?

This test is particularly important if your child shows:

  • Distinctive facial features (arched eyebrows, long eyelashes, flattened nose tip)
  • Developmental delays in speech, motor skills, or learning
  • Growth deficiencies or feeding difficulties
  • Skeletal abnormalities or joint laxity
  • Family history of similar symptoms or genetic conditions
  • Unexplained intellectual disability or behavioural challenges

Early detection through genetic testing can provide the roadmap for appropriate interventions and support services.

Why Early Detection Matters for Your Child’s Future

Getting a definitive diagnosis through our KDM6A test offers multiple life-changing benefits:

  • Peace of Mind: End the uncertainty and get clear answers about your child’s condition
  • Early Intervention: Access targeted therapies and educational support sooner
  • Family Planning: Understand inheritance patterns for future family decisions
  • Medical Management: Develop a comprehensive healthcare plan with your paediatrician
  • Community Support: Connect with other families facing similar challenges

Understanding Your Test Results

We know waiting for genetic test results can be anxiety-provoking. That’s why our process is designed to be as transparent and supportive as possible:

  • Clear Reporting: Your results will be presented in easy-to-understand language
  • Professional Interpretation: Our genetic counsellors will explain what the findings mean for your family
  • Next Steps Guidance: We’ll help you understand what to do with the information
  • Ongoing Support: Access to resources and referrals for specialist care

Remember: A positive result isn’t an endpoint – it’s the beginning of getting the right support for your child.

Transparent Pricing & Exceptional Value

Service Regular Price Special Price Savings
KDM6A Kabuki Syndrome NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650
Includes genetic counselling session and comprehensive result interpretation

Consider this investment in your child’s health: Early diagnosis can prevent years of uncertainty and potentially save thousands in unnecessary medical consultations and tests.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Partnering with leading paediatric genetic specialists
  • Advanced Technology: State-of-the-art NGS testing for maximum accuracy
  • Complete Confidentiality: Your family’s privacy is our absolute priority
  • Quick Turnaround: Results typically within 3-4 weeks
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s development continue. Every day without answers is a day without the right support. Our genetic counsellors are ready to guide you through this process with compassion and expertise.

Multiple Ways to Get Started:

  • Online Booking: Schedule your consultation and testing appointment
  • Phone Consultation: Speak directly with our genetic counselling team
  • Clinic Visit: Visit one of our nationwide testing centres

Limited Time Special: Book your KDM6A genetic test at the special price of ZAR 6,700 – a saving of ZAR 2,650 off the regular price. This offer won’t last forever.

“The relief of finally understanding our daughter’s condition was immeasurable. Oracle Genomics gave us the answers we needed to get her the right support.” – Johannesburg Parent