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DYNC1H1 Gene Spinal Muscular Atrophy Lower Extremity-Predominant Type 1 Genetic DNA Test

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

-28%

Facing concerns about spinal muscular atrophy or muscle weakness in your family? Our DYNC1H1 gene test provides definitive answers about your genetic risk for lower extremity-predominant spinal muscular atrophy. For just ZAR 6,700, you’ll receive comprehensive NGS genetic testing with professional genetic counselling to understand your family’s inheritance patterns. This advanced DNA analysis detects mutations in the DYNC1H1 gene that cause autosomal dominant SMA type 1, giving you the clarity needed for informed health decisions. Our trusted laboratory delivers results within 3-4 weeks, with nationwide coverage across South Africa including Johannesburg, Cape Town, and Durban. Take control of your genetic health with confidence through our accurate, patient-focused testing approach that prioritises your peace of mind.

📞 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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DYNC1H1 SMA Test South Africa | ZAR 6
DYNC1H1 Gene Spinal Muscular Atrophy Lower Extremity-Predominant Type 1 Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

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Find Clarity About Spinal Muscular Atrophy in Your Family

When muscle weakness runs in your family, the uncertainty can feel overwhelming. Our DYNC1H1 genetic test provides the definitive answers you need to understand your risk for lower extremity-predominant spinal muscular atrophy. For South African families facing these concerns, knowing your genetic status brings peace of mind and empowers informed health decisions.

Understanding Your DYNC1H1 Genetic Test

This advanced Next-Generation Sequencing (NGS) test specifically examines the DYNC1H1 gene for mutations that cause spinal muscular atrophy with lower limb predominance. Unlike standard genetic tests, our comprehensive analysis provides detailed information about autosomal dominant inheritance patterns, meaning the condition can be passed from one generation to the next with a 50% chance of transmission.

The test requires either a blood sample, extracted DNA, or a simple blood spot on an FTA card, making the process accessible and straightforward for patients across South Africa.

Who Should Consider This Genetic Test?

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

  • Progressive muscle weakness primarily affecting the legs and lower body
  • Difficulty with walking, running, or climbing stairs that began in childhood
  • Family history of similar muscle weakness patterns across generations
  • Concerns about passing genetic conditions to children
  • Unexplained muscle symptoms that neurologists have been unable to diagnose

Many South African patients find relief in finally understanding the genetic basis of their symptoms after years of uncertainty.

Why Early Genetic Detection Matters for Your Health

Identifying DYNC1H1 mutations early provides significant advantages:

  • Family Planning Confidence: Understand your 50% inheritance risk for future generations
  • Accurate Diagnosis: Move beyond symptom management to precise genetic understanding
  • Proactive Health Management: Work with neurologists to monitor and manage symptoms effectively
  • End Diagnostic Uncertainty: Replace years of unanswered questions with genetic clarity
  • Peace of Mind: Reduce anxiety about unexplained family health patterns

Understanding Your Test Results

Our genetic counselling team provides comprehensive support throughout your testing journey. Before your test, you’ll receive professional genetic counselling to create a detailed family pedigree chart, helping identify inheritance patterns. When your results are ready in 3-4 weeks, our specialists will:

  • Clearly explain what your DYNC1H1 gene results mean for your health
  • Discuss inheritance patterns and family implications
  • Provide guidance on next steps and specialist referrals
  • Answer all your questions in plain, understandable language
  • Offer emotional support and resources for moving forward

Whether your results are positive or negative, you’ll leave with clarity and a concrete plan.

Transparent Pricing & Exceptional Value

Service Regular Price Special Price Savings
DYNC1H1 Genetic Test with Genetic Counselling ZAR 9,350 ZAR 6,700 ZAR 2,650

Your investment includes: Comprehensive NGS genetic analysis, pre-test genetic counselling session, detailed results interpretation, and ongoing support. Consider the value of ending years of diagnostic uncertainty and gaining control over your family’s health future.

Why South Africans Trust Oracle Genomics

  • Nationwide Coverage: Accessible testing across Johannesburg, Cape Town, Durban, Pretoria and throughout South Africa
  • Neurology Specialisation: Tests developed and interpreted by neurological genetics experts
  • Advanced NGS Technology: Most accurate genetic testing available today
  • Complete Confidentiality: Your genetic information remains private and secure
  • Proven Accuracy: Reliable results you can trust for major health decisions
  • South African Focus: Understanding of local healthcare needs and family dynamics

Take the First Step Toward Genetic Clarity Today

Don’t let uncertainty about spinal muscular atrophy control your family’s future. Our compassionate team is ready to guide you through this important genetic testing process with professionalism and understanding.

Multiple Ways to Book Your Test:

  • Online Booking: Secure instant appointment scheduling
  • Telephone Consultation: Speak directly with our genetic counselling team
  • Clinic Visit: Personal consultation at our facilities nationwide

Limited Time Special: Book now to secure your ZAR 6,700 pricing before this offer ends. Take control of your genetic health journey with confidence and professional support every step of the way.

“Getting our DYNC1H1 test results finally explained why three generations of our family struggled with leg weakness. The genetic counselling helped us understand everything clearly.” – Satisfied Patient, Cape Town