Find Clarity About Muscle Weakness and Genetic Risk
When you notice unexplained muscle weakness or have concerns about family history of muscular conditions, it’s natural to feel anxious and uncertain. Our FKTN Gene Limb-Girdle Muscular Dystrophy Type 2M test provides the answers you need to move forward with confidence and peace of mind.
Understanding Your FKTN Gene Test
This advanced genetic test examines the FKTN gene using Next Generation Sequencing (NGS) technology to identify mutations that cause Limb-Girdle Muscular Dystrophy Type 2M. This inherited condition affects the muscles around your shoulders and hips, and understanding your genetic status can help you and your healthcare team develop the right management plan.
The test is specifically designed to detect autosomal recessive inheritance patterns, meaning both parents must carry the gene mutation for the condition to be passed on to children.
Who Should Consider This Test?
This test is particularly important if you experience:
- Progressive muscle weakness in shoulders, hips, or thighs
- Difficulty climbing stairs or rising from chairs
- Family history of muscular dystrophy or unexplained muscle conditions
- Planning pregnancy with concerns about genetic inheritance
- Unexplained elevated creatine kinase levels
- Children showing delayed motor milestones
Many South Africans live with undiagnosed muscle conditions – getting tested can provide the clarity needed for proper management and treatment.
Why Early Detection Matters for Your Health
Knowing your genetic status empowers you to:
- Access appropriate medical care and management strategies
- Make informed family planning decisions
- Connect with specialist neurologists and support services
- Participate in clinical trials and emerging treatments
- Reduce anxiety through definitive answers
- Plan for future healthcare needs with confidence
Early detection can significantly improve quality of life by enabling proactive management of symptoms.
Understanding Your Test Results
Our comprehensive genetic counselling ensures you fully understand your results and their implications:
- Positive Result: Indicates the presence of FKTN gene mutations. Our genetic counsellors will explain what this means for your health and connect you with appropriate specialists.
- Negative Result: No FKTN gene mutations detected, providing peace of mind about this specific condition.
- Carrier Status: You carry one copy of the mutation but won’t develop the condition yourself – important information for family planning.
All results come with professional interpretation and guidance for next steps.
Transparent Pricing – Excellent Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| FKTN Gene Test | ZAR 6,700 | ZAR 2,650 |
Includes genetic counselling, sample collection, and comprehensive result interpretation
Why Trust Oracle Genomics?
- Nationwide Coverage: Available in Johannesburg, Cape Town, Durban, Pretoria and across South Africa
- Expert Team: Specialist neurologists and certified genetic counsellors
- Advanced Technology: Next Generation Sequencing for maximum accuracy
- Quick Turnaround: Results in 3-4 weeks
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- Professional Support: Comprehensive genetic counselling included
Take the First Step Toward Clarity
Don’t let uncertainty about muscle weakness or family history hold you back. Our FKTN Gene Test provides the answers you need to make informed decisions about your health and future.
Limited Time Offer: Save ZAR 2,650 on this comprehensive genetic test. Early detection can make a significant difference in managing muscular conditions.
