Limb-Girdle Muscular Dystrophy Genetic Testing
Understanding Limb-Girdle Muscular Dystrophy
Limb-Girdle Muscular Dystrophy (LGMD) represents a diverse group of inherited muscle disorders characterized by progressive weakness and wasting of muscles primarily affecting the shoulder and hip girdles. This comprehensive genetic test provides crucial diagnostic information for individuals experiencing unexplained muscle weakness, helping to differentiate LGMD from other neuromuscular conditions and enabling targeted treatment approaches.
What Our Test Measures
Our advanced genetic analysis examines multiple genes associated with Limb-Girdle Muscular Dystrophy, including:
- Calpain-3 (CAPN3) gene mutations
- Dysferlin (DYSF) gene variants
- Sarcoglycan complex genes (SGCA, SGCB, SGCD, SGCE)
- Fukutin-related protein (FKRP) mutations
- Anoctamin-5 (ANO5) gene analysis
- Additional LGMD-associated genetic markers
Who Should Consider This Test
This genetic test is recommended for individuals experiencing:
- Progressive weakness in hip and shoulder muscles
- Difficulty climbing stairs or rising from chairs
- Waddling gait or frequent falls
- Muscle wasting in the thighs and upper arms
- Family history of muscular dystrophy
- Elevated creatine kinase levels without clear cause
- Unexplained muscle pain or cramping
Benefits of Genetic Testing
Accurate Diagnosis
Genetic testing provides definitive diagnosis, eliminating the uncertainty of clinical assessments alone and reducing the need for invasive muscle biopsies.
Family Planning Guidance
Understanding your genetic status helps assess risks for future generations and enables informed family planning decisions.
Personalized Treatment Approaches
Specific genetic diagnoses allow for targeted therapeutic interventions and participation in relevant clinical trials.
Proactive Health Management
Early diagnosis facilitates timely interventions, including physical therapy, respiratory support, and cardiac monitoring when indicated.
Understanding Your Test Results
Our comprehensive genetic analysis provides clear, actionable results:
- Positive Result: Identifies specific genetic mutations confirming LGMD diagnosis, allowing for subtype classification and targeted management
- Negative Result: Rules out common LGMD genetic causes, guiding further diagnostic evaluation for other neuromuscular conditions
- Variant of Uncertain Significance: Identifies genetic changes requiring additional family studies or clinical correlation
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Limb-Girdle Muscular Dystrophy Genetic Test | $350 USD | $426 USD |
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving patients in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures accessible genetic testing services regardless of your location.
Take Control of Your Health Today
Don’t let uncertainty about muscle weakness affect your quality of life. Our comprehensive Limb-Girdle Muscular Dystrophy genetic test provides the answers you need for proper diagnosis and management. Early detection through genetic testing can significantly impact treatment outcomes and quality of life.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation. Our genetic counselors are available to answer your questions and guide you through the testing process.
Take the first step toward understanding your genetic health and receiving the personalized care you deserve. Book your Limb-Girdle Muscular Dystrophy genetic test now and gain clarity about your neuromuscular health.
