Find Clarity About Your Muscle Weakness Symptoms
When unexplained muscle weakness affects your daily life, it’s natural to feel concerned and uncertain. Our FAT1 Gene Facioscapulohumeral Dystrophy-Like Phenotype test provides the answers you need to move forward with confidence. Using cutting-edge genetic technology, we help identify the underlying causes of your symptoms, giving you and your healthcare team the information needed for proper management.
Understanding Your FAT1 Gene Test
The FAT1 gene plays a crucial role in muscle development and function. When mutations occur in this gene, they can lead to symptoms that resemble Facioscapulohumeral Dystrophy (FSHD), including progressive muscle weakness in the face, shoulders, and upper arms. Our Next-Generation Sequencing (NGS) technology examines your FAT1 gene with exceptional accuracy, providing clear insights into whether genetic factors are contributing to your symptoms.
This isn’t just a test – it’s a pathway to understanding your body better and making informed decisions about your health journey.
Who Should Consider This Test?
This test may be right for you if you experience:
- Progressive weakness in facial muscles, shoulders, or upper arms
- Difficulty raising your arms overhead or closing your eyes completely
- Family history of muscular conditions or unexplained weakness
- Muscle symptoms that began in teenage or early adult years
- Concerns about passing genetic conditions to children
Many South Africans live with these symptoms for years without clear answers. Our test provides the clarity needed to stop guessing and start managing.
Why Early Detection Matters for Your Health
Getting answers about your genetic makeup empowers you to:
- Develop targeted management strategies with your neurologist
- Make informed family planning decisions
- Access appropriate support services and resources
- Reduce anxiety through definitive diagnosis
- Monitor symptoms more effectively with proper understanding
Early detection means you can take proactive steps to maintain your quality of life and manage symptoms effectively.
Understanding Your Results with Confidence
We know waiting for genetic test results can be stressful. That’s why we provide:
- Clear, easy-to-understand reports with your neurologist
- Genetic counselling to help interpret results in context
- Guidance on next steps based on your specific situation
- Support in understanding what results mean for your family
Your results will clearly indicate whether FAT1 gene mutations were detected and what this means for your health management.
Transparent Pricing – No Surprises
| Service | Regular Price | Special Price |
|---|---|---|
| FAT1 Gene FSHD-Like Test | ZAR 6,700 | |
| Genetic Counselling Session | Included | |
| Family Pedigree Analysis | Included | |
| Results Consultation | Included | |
Turnaround time: 3-4 weeks | Sample: Blood, Extracted DNA, or Blood on FTA Card
Why Trust Oracle Genomics?
- Nationwide Coverage: Accessible testing across South Africa including Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Tests supervised by qualified neurologists and genetic specialists
- Advanced Technology: State-of-the-art NGS technology for maximum accuracy
- Patient-Focused Care: Genetic counselling included to support your journey
- Proven Reliability: Trusted by healthcare professionals nationwide
Take the First Step Toward Clarity
Don’t let uncertainty about your symptoms control your life. Our FAT1 Gene test provides the answers you need to move forward with confidence.
Limited time special pricing: Save ZAR 2,650 while gaining peace of mind about your health.
