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SLC22A5 Gene Carnitine Deficiency NGS Genetic DNA Test

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

-28%

If you’re concerned about carnitine deficiency or have family members affected by this condition, our SLC22A5 Gene Carnitine Deficiency NGS Genetic DNA Test provides the answers you need for just ZAR 6,700. This comprehensive test uses advanced Next-Generation Sequencing technology to detect mutations in the SLC22A5 gene, which is responsible for carnitine transport in your body. Early detection can prevent serious complications like muscle weakness, heart problems, and metabolic crises. Our test is particularly valuable for families with a history of carnitine deficiency or individuals experiencing unexplained fatigue and muscle issues. With results available in 3-4 weeks and genetic counselling included, you’ll gain clarity about your genetic health. We serve patients across South Africa, including Johannesburg, Cape Town, and Durban, with the same trusted accuracy and care. Take control of your health journey with confidence in our reliable testing process.

📞 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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SLC22A5 Carnitine Deficiency DNA Test | ZAR 6
SLC22A5 Gene Carnitine Deficiency NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Understanding Your Genetic Risk for Carnitine Deficiency

If you’ve been experiencing unexplained fatigue, muscle weakness, or have family members affected by carnitine deficiency, you’re not alone in your concerns. Many South Africans worry about inherited metabolic conditions and their impact on daily life. Our SLC22A5 Gene Carnitine Deficiency NGS Genetic DNA Test provides the clarity and peace of mind you deserve, using cutting-edge technology to give you accurate answers about your genetic health.

What This Test Detects

The SLC22A5 gene plays a crucial role in transporting carnitine throughout your body – an essential nutrient that helps convert fat into energy. When this gene has mutations, it can lead to primary carnitine deficiency, a condition where your body struggles to use fats for energy properly. Our advanced Next-Generation Sequencing (NGS) technology examines your DNA to identify any variations in the SLC22A5 gene that might affect your carnitine levels and overall metabolic health.

Who Should Consider This Test

This test is particularly important if you experience:

  • Unexplained fatigue or low energy levels
  • Muscle weakness or pain without clear cause
  • Family history of carnitine deficiency or metabolic disorders
  • Children with developmental delays or feeding difficulties
  • History of low blood sugar or metabolic crises
  • Unexplained heart muscle problems

Many patients from Johannesburg to Cape Town find that understanding their genetic risk helps them make informed decisions about their health management.

Why Early Detection Matters for Your Health

Discovering carnitine deficiency early can be life-changing. With proper diagnosis:

  • You can prevent serious metabolic crises that require hospitalisation
  • Simple dietary changes and carnitine supplements can manage the condition effectively
  • You reduce the risk of heart muscle damage and liver problems
  • Children can avoid developmental delays with early intervention
  • Family members can be screened and protected from potential complications

Early detection transforms uncertainty into actionable health plans.

Understanding Your Results with Confidence

When your results are ready in 3-4 weeks, our team provides clear, understandable explanations. We don’t just give you numbers – we help you understand what they mean for your health. If the test identifies a mutation, we’ll guide you through next steps, including dietary management and treatment options. If no mutations are found, you’ll have peace of mind knowing your carnitine transport system is functioning normally. Our genetic counselling ensures you never feel alone in interpreting your results.

Transparent Pricing – Your Health Investment

Service Regular Price Special Price
SLC22A5 Carnitine Deficiency DNA Test ZAR 9,350 ZAR 6,700

This investment in your health includes comprehensive genetic counselling, advanced NGS testing, and detailed result interpretation – potentially saving you from costly emergency treatments and hospital stays down the line.

Why Trust Oracle Genomics

We serve patients across South Africa with the same commitment to accuracy and care:

  • Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
  • Advanced Technology: Using reliable NGS methods for precise results
  • Expert Guidance: Genetic counselling included with every test
  • Proven Accuracy: Trusted by healthcare professionals nationwide
  • Patient-Focused: We understand the emotional journey of genetic testing

Take the First Step Toward Genetic Clarity

Don’t let uncertainty about carnitine deficiency affect your quality of life. Our team is ready to support you through this important health journey with compassion and expertise.

Multiple Ways to Book Your Test

  • Online Booking: Secure your appointment in minutes
  • Phone Consultation: Speak directly with our genetic specialists
  • Clinic Visit: Convenient locations across major cities

Sample Collection Options: We offer flexible testing methods including blood draw, extracted DNA, or simple finger-prick blood collection on FTA cards for your convenience.

Every day you wait is another day without answers. Take control of your genetic health today and gain the peace of mind that comes with knowing your carnitine status. Our special pricing of ZAR 6,700 makes this essential health investment accessible to South African families who need clarity about their metabolic health.

“Knowledge about your genetic health is the first step toward empowered living.”