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CA5A Gene Hyperammonemia Carbonic Anhydrase VA Deficiency NGS Genetic DNA Test

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

-28%

Facing unexplained neurological symptoms or metabolic concerns? Our CA5A Gene Hyperammonemia NGS Genetic DNA Test provides definitive answers about carbonic anhydrase VA deficiency. For just ZAR 6,700, you’ll receive comprehensive genetic analysis using advanced NGS technology, combined with professional genetic counselling to understand your family’s health patterns. This test is crucial for South Africans experiencing developmental delays, seizures, or metabolic disorders that may indicate this rare genetic condition. Our expert team ensures accurate results within 3-4 weeks, giving you the clarity needed to make informed health decisions. With nationwide coverage including Johannesburg, Cape Town, and Durban, accessing this specialised testing has never been easier. Trust Oracle Genomics for reliable genetic testing that puts your health journey first.

📞 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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CA5A Gene Hyperammonemia Test ZAR 6
CA5A Gene Hyperammonemia Carbonic Anhydrase VA Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding CA5A Gene Hyperammonemia: Your Path to Clarity

When unexplained neurological symptoms or metabolic concerns affect your family’s wellbeing, finding answers becomes your top priority. Our CA5A Gene Hyperammonemia NGS Genetic DNA Test offers the definitive clarity you need about carbonic anhydrase VA deficiency – a rare genetic condition that can impact neurological development and metabolic function. We understand the anxiety that comes with unexplained health challenges, which is why we’ve created a comprehensive testing experience that combines cutting-edge technology with compassionate care.

What This Test Detects

The CA5A Gene Hyperammonemia test examines your genetic makeup for mutations in the CA5A gene, which provides instructions for making carbonic anhydrase VA enzyme. This enzyme plays a crucial role in the urea cycle – your body’s natural process for removing ammonia. When this enzyme doesn’t function properly, ammonia can build up to dangerous levels, potentially causing neurological damage and developmental challenges. Our advanced Next-Generation Sequencing (NGS) technology provides the most accurate analysis available, giving you reliable results you can trust.

Who Should Consider This Test?

This test is particularly important if you or your family members experience:

  • Unexplained developmental delays in infants or children
  • Recurrent episodes of lethargy or vomiting
  • Seizures without clear cause
  • Metabolic acidosis or hyperammonemia
  • Family history of similar neurological or metabolic conditions
  • Poor feeding or failure to thrive in infancy

Many South African families have found answers through this testing, gaining the understanding needed to manage their health effectively.

Why Early Detection Matters for Your Health

Identifying CA5A gene mutations early can transform your health journey by:

  • Enabling proactive management strategies to prevent ammonia buildup
  • Guiding appropriate dietary and medical interventions
  • Providing clarity for family planning decisions
  • Reducing the risk of neurological damage through early intervention
  • Offering peace of mind through definitive diagnosis

Early detection means you can take control of your health before symptoms escalate, potentially preventing serious complications.

Understanding Your Results with Compassion

We know that waiting for genetic test results can be anxiety-provoking. That’s why our process includes comprehensive genetic counselling both before and after testing. Our certified genetic counsellors will help you understand:

  • What your specific genetic findings mean for your health
  • How to interpret the results in the context of your symptoms
  • Next steps for management and treatment options
  • Implications for family members
  • Available support resources in South Africa

Your results will be presented in clear, understandable language with personalised recommendations from our medical team.

Transparent Pricing – Exceptional Value

Service Regular Price Special Price Savings
CA5A Gene Hyperammonemia NGS Test ZAR 9,350 ZAR 6,700 ZAR 2,650

What’s Included:

  • Comprehensive NGS genetic analysis
  • Pre-test genetic counselling session
  • Professional pedigree chart creation
  • Post-test results explanation
  • 3-4 week turnaround time
  • Multiple sample options (blood, DNA, or FTA card)

Why Trust Oracle Genomics?

As South Africa’s leading genetic testing provider, we bring you:

  • Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
  • Medical Expertise: Tests supervised by qualified general physicians and genetic specialists
  • Advanced Technology: State-of-the-art NGS technology ensuring 99.9% accuracy
  • Patient-Centred Care: Empathetic support throughout your testing journey
  • Proven Track Record: Thousands of South African families served with reliable results

Take the First Step Toward Clarity Today

Don’t let uncertainty about your health continue. Early detection of CA5A gene mutations can make a significant difference in managing your condition effectively. Our special pricing of ZAR 6,700 makes this comprehensive testing more accessible than ever.

Multiple Ways to Book Your Test:

  • Online Booking: Secure your appointment through our website 24/7
  • Telephone Consultation: Speak directly with our genetic counsellors
  • In-Person Visit: Visit our centres in major cities nationwide

Limited Time Offer: This special pricing of ZAR 6,700 (regularly ZAR 9,350) won’t last forever. Take advantage of these savings while investing in your family’s health future.

Contact Oracle Genomics today and begin your journey to understanding with confidence and compassion.