PRDM16 Gene Cardiomyopathy Dilated Type 1LL NGS Genetic DNA Test
Comprehensive Genetic Testing for Inherited Heart Conditions
The PRDM16 Gene Cardiomyopathy Dilated Type 1LL NGS Genetic DNA Test represents a breakthrough in cardiac genetic diagnostics, offering precise detection of mutations associated with dilated cardiomyopathy. This inherited condition affects the heart’s ability to pump blood effectively, potentially leading to serious cardiovascular complications if left undiagnosed.
What This Advanced Genetic Test Measures
Our state-of-the-art NGS (Next-Generation Sequencing) technology specifically targets the PRDM16 gene, which plays a critical role in cardiac muscle development and function. The test identifies:
- Pathogenic variants in the PRDM16 gene associated with dilated cardiomyopathy type 1LL
- Single nucleotide polymorphisms (SNPs) affecting cardiac muscle structure
- Insertions and deletions that disrupt normal gene function
- Copy number variations impacting cardiac development
Who Should Consider This Genetic Test
This comprehensive genetic analysis is recommended for individuals experiencing:
- Unexplained heart enlargement or cardiomyopathy symptoms
- Family history of sudden cardiac death or heart failure
- Progressive shortness of breath and fatigue during physical activity
- Swelling in legs, ankles, or feet due to fluid retention
- Irregular heart rhythms or palpitations without clear cause
- Multiple family members diagnosed with heart muscle disease
Significant Benefits of Early Genetic Detection
Early identification of PRDM16 gene mutations provides numerous advantages:
- Proactive Treatment Planning: Enables targeted medical interventions before severe symptoms develop
- Family Screening: Identifies at-risk relatives who may benefit from preventive care
- Personalized Medication: Guides selection of appropriate cardiac medications and therapies
- Lifestyle Modifications: Informs decisions about physical activity levels and dietary changes
- Reproductive Planning: Provides crucial information for family planning decisions
Understanding Your Genetic Test Results
Our comprehensive genetic counseling helps you interpret your results effectively:
- Positive Result: Indicates presence of PRDM16 mutation; requires cardiac specialist consultation and regular monitoring
- Negative Result: No detected mutation; however, continued cardiac health monitoring remains important
- Variant of Uncertain Significance: Requires additional family testing and ongoing research correlation
- Clinical Correlation: Results should always be interpreted in context of personal and family medical history
Test Pricing and Availability
| Test Description | Price (USD) |
|---|---|
| PRDM16 Gene Cardiomyopathy Dilated Type 1LL NGS Genetic DNA Test – Discount Price | $500 |
| PRDM16 Gene Cardiomyopathy Dilated Type 1LL NGS Genetic DNA Test – Regular Price | $700 |
Nationwide Testing Accessibility
GGC DNA maintains comprehensive testing facilities across the United States, with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, and Philadelphia. Our certified genetic counselors and cardiac specialists ensure you receive personalized care and accurate results.
Take Control of Your Cardiac Health Today
Don’t wait for symptoms to escalate. Early genetic detection of PRDM16 mutations can significantly impact your long-term cardiovascular health and quality of life. Our experienced team is ready to guide you through the testing process and provide the comprehensive care you deserve.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your PRDM16 Gene Cardiomyopathy Dilated Type 1LL NGS Genetic DNA Test. Take the first step toward proactive cardiac health management with GGC DNA’s advanced genetic testing services.
