SNCA Gene PARK4 Parkinson NGS Genetic DNA Test
Comprehensive Genetic Testing for Parkinson’s Disease Risk Assessment
The SNCA Gene PARK4 Parkinson NGS Genetic DNA Test represents a breakthrough in neurological genetic testing, offering individuals and families unprecedented insights into Parkinson’s disease risk factors. This advanced diagnostic tool utilizes cutting-edge Next-Generation Sequencing (NGS) technology to analyze the SNCA (alpha-synuclein) gene, which plays a critical role in Parkinson’s disease development and progression.
What Does This Test Measure?
This comprehensive genetic test specifically targets mutations and variations in the SNCA gene, also known as the PARK4 locus. The test detects:
- Point mutations in the SNCA gene coding regions
- Gene duplications and triplications associated with Parkinson’s disease
- Single nucleotide polymorphisms (SNPs) linked to increased disease risk
- Copy number variations affecting alpha-synuclein protein production
- Genetic markers associated with early-onset Parkinson’s disease
Who Should Consider This Test?
This genetic screening is particularly recommended for individuals experiencing:
- Family history of Parkinson’s disease in first-degree relatives
- Early-onset movement disorders or tremors
- Unexplained neurological symptoms before age 50
- Multiple family members affected by Parkinson’s disease
- Individuals planning family with known Parkinson’s risk factors
- Patients with atypical Parkinsonism symptoms
Key Benefits of Genetic Testing
Undergoing the SNCA Gene PARK4 Parkinson NGS Genetic DNA Test provides numerous advantages:
- Early Risk Assessment: Identify genetic predisposition before symptom onset
- Personalized Treatment Planning: Tailor medical interventions based on genetic profile
- Family Planning Guidance: Make informed decisions about family health
- Proactive Health Management: Implement preventive strategies and lifestyle modifications
- Reduced Diagnostic Uncertainty: Clarify ambiguous neurological symptoms
- Research Contribution: Advance scientific understanding of Parkinson’s genetics
Understanding Your Test Results
Your genetic test results will be carefully interpreted by our team of certified genetic counselors and neurologists. Results typically fall into three categories:
- Positive Result: Indicates presence of known Parkinson’s-associated mutations, requiring comprehensive follow-up care and monitoring
- Negative Result: No detected mutations in tested genes, though does not eliminate all Parkinson’s disease risk
- Variant of Uncertain Significance: Genetic changes with unclear clinical implications requiring ongoing research and monitoring
Test Pricing Information
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities. Our network of certified collection centers ensures accessible genetic testing services nationwide.
Take Control of Your Neurological Health
Don’t wait to gain valuable insights into your genetic risk factors for Parkinson’s disease. Our comprehensive SNCA Gene PARK4 Parkinson NGS Genetic DNA Test provides the information you need to make informed healthcare decisions and proactively manage your neurological health.
Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our genetic specialists are ready to guide you through the testing process and help you understand your results.
Turnaround Time: 3-4 Weeks | Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
