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SLC13A5 Gene Early Infantile Epileptic Encephalopathy Type 25 NGS Genetic DNA Test

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

-28%

Facing concerns about your infant’s neurological development? Our SLC13A5 Gene Test provides definitive answers for early infantile epileptic encephalopathy type 25. Using advanced NGS technology, this comprehensive genetic analysis detects mutations in the SLC13A5 gene that cause severe epilepsy in infants. For just ZAR 6,700 (regularly ZAR 9,350), you’ll receive accurate results within 3-4 weeks, giving you the clarity needed for proper treatment planning. Our test is especially crucial for infants showing developmental delays, seizures, or abnormal movements in their first months. With nationwide coverage including Johannesburg, Cape Town, and Durban, we make advanced genetic testing accessible across South Africa. Trust our experienced neurologists and genetic counsellors to guide you through this important health journey with compassion and expertise.

📞 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

SLC13A5 Gene Test ZAR 6
SLC13A5 Gene Early Infantile Epileptic Encephalopathy Type 25 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 Infant’s Neurological Health

When your baby shows signs of developmental concerns or unusual movements, the uncertainty can be overwhelming. Our SLC13A5 Gene Test provides the clarity you need to understand and address early infantile epileptic encephalopathy type 25 – a rare but serious genetic condition affecting infants in their first months of life.

Understanding the SLC13A5 Gene Test

This advanced genetic test uses Next-Generation Sequencing (NGS) technology to examine the SLC13A5 gene, which plays a crucial role in brain development and function. When this gene contains mutations, it can lead to early infantile epileptic encephalopathy type 25 – a condition characterised by seizures that begin in the first days or weeks of life, often accompanied by developmental delays.

Our test provides definitive answers by identifying specific genetic variations that may be causing your infant’s symptoms, allowing for targeted treatment approaches and better health outcomes.

Who Should Consider This Test?

This test is particularly important for infants showing:

  • Seizures beginning in the first weeks or months of life
  • Developmental delays or regression
  • Abnormal muscle tone or movements
  • Feeding difficulties
  • Family history of similar neurological conditions
  • Unexplained developmental concerns

If your infant has been experiencing any of these symptoms, early genetic testing can provide crucial information for their healthcare team.

Why Early Detection Matters for Your Infant’s Future

Getting an accurate diagnosis through genetic testing offers multiple benefits:

  • Targeted Treatment: Knowing the specific genetic cause allows doctors to develop more effective treatment plans
  • Early Intervention: Prompt diagnosis enables early therapeutic interventions that can improve developmental outcomes
  • Family Planning: Understanding the genetic basis helps with family planning decisions
  • Peace of Mind: Replacing uncertainty with clear answers reduces parental stress and anxiety
  • Better Care Coordination: Accurate diagnosis helps coordinate care among multiple specialists

Understanding Your Test Results

We understand that waiting for genetic test results can be anxiety-provoking. Our process includes:

  • Genetic Counselling: Before testing, you’ll meet with a genetic counsellor who will create a detailed family history and explain what to expect
  • Clear Reporting: Results are presented in easy-to-understand language with guidance from our neurologists
  • Comprehensive Support: We provide ongoing support and resources regardless of your results
  • Fast Turnaround: Most results are available within 3-4 weeks

Our team is here to support you every step of the way, ensuring you fully understand your results and their implications.

Affordable, Accessible Genetic Testing

Test Feature Details Value
Regular Price ZAR 9,350 Comprehensive genetic analysis
Special Price ZAR 6,700 Save ZAR 2,650
Turnaround Time 3-4 Weeks Fast results for timely decisions
Sample Type Blood, Extracted DNA, or Blood on FTA Card Convenient options for infants

Considering the potential lifelong impact of early diagnosis, this test represents excellent value for your infant’s health future.

Why Trust Oracle Genomics?

  • Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
  • Expert Neurologists: Our tests are developed and interpreted by specialist neurologists
  • Advanced Technology: Using NGS technology for the highest accuracy available
  • Genetic Counselling: Comprehensive pre- and post-test counselling included
  • Proven Accuracy: Reliable results you can trust for important health decisions
  • Patient-Focused Care: We understand the emotional journey of genetic testing

Take the First Step Toward Answers Today

Don’t let uncertainty about your infant’s health create unnecessary stress. Early detection through genetic testing can make a significant difference in treatment outcomes and quality of life.

Book your SLC13A5 Gene Test now and take advantage of our special ZAR 6,700 pricing. Our team is ready to provide the compassionate, professional care your family deserves.



Limited time special pricing – secure your infant’s health future today