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CDKL5 Gene Angelman-like Syndrome NGS Genetic DNA Test

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

-28%

Facing concerns about developmental delays, seizures, or neurological symptoms in your child? The CDKL5 Gene Angelman-like Syndrome NGS Genetic DNA Test provides the answers you need for peace of mind and proper healthcare planning. This comprehensive genetic test uses advanced Next Generation Sequencing technology to detect mutations in the CDKL5 gene, which can cause severe developmental disorders resembling Angelman syndrome. For just ZAR 6,700, you gain access to highly accurate results that can guide treatment decisions and provide clarity for your family’s future. Our test is specifically designed for South African families experiencing unexplained developmental delays, early-onset seizures, or movement disorders. With results delivered within 3-4 weeks and nationwide coverage including Johannesburg, Cape Town, and Durban, we make genetic testing accessible and trustworthy. Take the first step toward understanding your child’s health journey with confidence and professional medical support.

📞 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

CDKL5 Gene Angelman-like Syndrome Test | ZAR 6
CDKL5 Gene Angelman-like Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Answers for Your Child’s Developmental Journey

When your child faces unexplained developmental delays, seizures, or movement challenges, the uncertainty can feel overwhelming. The CDKL5 Gene Angelman-like Syndrome Test provides the clarity and direction your family deserves. Using cutting-edge genetic technology, we help South African families understand complex neurological conditions and create effective care plans.

Understanding Your CDKL5 Genetic Test

The CDKL5 gene plays a crucial role in brain development and function. When mutations occur in this gene, they can cause symptoms similar to Angelman syndrome, including severe developmental delays, early-onset seizures, and movement disorders. Our Next Generation Sequencing (NGS) technology examines this gene with exceptional accuracy, providing reliable results that can guide your child’s healthcare journey.

This isn’t just a test – it’s a pathway to understanding. By identifying the specific genetic cause of symptoms, families can move from uncertainty to informed action, accessing targeted therapies and support services.

Is This Test Right for Your Family?

This test is specifically recommended for children and individuals showing:

  • Unexplained developmental delays or regression
  • Early-onset seizures (often beginning in infancy)
  • Movement disorders or coordination difficulties
  • Features resembling Angelman syndrome without confirmed diagnosis
  • Family history of similar neurological conditions
  • Speech and communication challenges

If you’ve been searching for answers about your child’s neurological development, this test could provide the breakthrough you need.

Why Early Detection Matters for Your Child’s Future

Getting a precise genetic diagnosis offers more than just answers – it opens doors to better care and support:

  • Targeted Treatment Plans: Knowing the specific genetic cause allows healthcare providers to create personalised intervention strategies
  • Early Intervention Opportunities: Access specialised therapies and educational support sooner
  • Family Planning Guidance: Understand inheritance patterns for future family planning decisions
  • Reduced Diagnostic Odyssey: Avoid years of uncertainty and multiple specialist visits
  • Connection to Support Networks: Join specific condition communities and access tailored resources

Understanding Your Results with Confidence

We know waiting for genetic test results can be anxiety-provoking. That’s why we provide:

  • Clear, Comprehensive Reports: Results explained in understandable language with medical guidance
  • Genetic Counselling Support: Professional interpretation of what your results mean for your family
  • Next Steps Guidance: Practical recommendations for healthcare providers and support services
  • Ongoing Support: Access to resources and information as you navigate your child’s care journey

Your results will be delivered within 3-4 weeks, and our team is here to help you understand every aspect of the report.

Affordable, Accessible Genetic Testing for South African Families

Test Option Price Value
Special Price ZAR 6,700 Limited time offer
Regular Price ZAR 9,350 Standard rate

Consider the long-term value: Early diagnosis can save thousands in unnecessary tests and treatments while providing the right support from the beginning.

Why South African Families Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
  • Advanced Technology: State-of-the-art NGS sequencing for maximum accuracy
  • Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
  • Comprehensive Preparation: Includes genetic counselling and family history assessment
  • Proven Track Record: Trusted by healthcare providers nationwide

Take the First Step Toward Clarity Today

Don’t let uncertainty about your child’s development continue. With our special pricing of ZAR 6,700, there’s never been a better time to get the answers you need.



Limited Time Offer: Special pricing of ZAR 6,700 available for a limited period. Regular price ZAR 9,350.

Available at testing centres throughout South Africa including Johannesburg, Cape Town, Durban, and Pretoria. Results delivered within 3-4 weeks.