PSEN1 Gene Dementia Frontotemporal NGS Genetic DNA Test
Comprehensive Genetic Assessment for Dementia Risk
The PSEN1 Gene Dementia Frontotemporal NGS Genetic DNA Test represents a breakthrough in neurological genetic testing, offering individuals and families crucial insights into their genetic predisposition for frontotemporal dementia and related neurodegenerative conditions. This advanced diagnostic tool utilizes cutting-edge Next-Generation Sequencing (NGS) technology to analyze the PSEN1 gene, which plays a critical role in the development of early-onset familial Alzheimer’s disease and frontotemporal dementia.
What This Test Measures and Detects
This comprehensive genetic analysis specifically targets mutations in the PSEN1 (Presenilin 1) gene, which encodes a protein essential for gamma-secretase complex function. The test identifies:
- Pathogenic variants associated with autosomal dominant Alzheimer’s disease
- Mutations linked to frontotemporal dementia development
- Genetic markers for early-onset neurodegenerative conditions
- Inheritance patterns affecting family members
- Specific nucleotide changes and protein alterations
Who Should Consider This Genetic Test
This test is particularly recommended for individuals experiencing or concerned about:
- Progressive memory loss beginning before age 65
- Family history of early-onset dementia or Alzheimer’s disease
- Personality changes, behavioral disturbances, or language difficulties
- Progressive cognitive decline with unknown cause
- Planning for family genetic counseling and risk assessment
- Unexplained neurological symptoms in multiple family members
Significant Benefits of Genetic Testing
Undergoing the PSEN1 genetic test provides numerous advantages for patients and their families:
- Early Risk Identification: Detect genetic predisposition before symptom onset
- Family Planning Guidance: Make informed decisions about genetic inheritance
- Personalized Medical Management: Develop targeted monitoring and prevention strategies
- Psychological Preparation: Reduce uncertainty and anxiety about genetic risk
- Clinical Trial Eligibility: Qualify for emerging treatments and research studies
- Comprehensive Genetic Counseling: Professional interpretation of complex results
Understanding Your Test Results
Our genetic specialists provide detailed guidance on interpreting your PSEN1 test results:
- Positive Result: Indicates presence of a known pathogenic mutation, requiring comprehensive genetic counseling and specialized neurological care
- Negative Result: No detected mutations in the PSEN1 gene, though continued monitoring may be recommended based on family history
- Variant of Uncertain Significance: Requires ongoing research and periodic re-evaluation as scientific knowledge advances
- Professional Interpretation: All results include detailed consultation with our certified genetic counselors
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
Nationwide Accessibility and Support
We maintain comprehensive testing facilities across major metropolitan areas throughout the United States, including New York City, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures convenient access to advanced genetic testing services regardless of your location.
Take Control of Your Neurological Health Today
Don’t let uncertainty about genetic risk compromise your future health planning. Our team of neurological genetics specialists and certified genetic counselors are ready to guide you through the testing process and help you understand your results. Early detection through genetic testing can provide valuable time for intervention planning and family preparation.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your PSEN1 Gene Dementia Frontotemporal NGS Genetic DNA Test. Take the first step toward understanding your genetic risk and securing your neurological health future.
