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UCHL1 Gene PARK5 Parkinson Genetic Test

Original price was: $700.Current price is: $500.

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The UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test is a cutting-edge genetic screening that identifies mutations in the UCHL1 gene associated with PARK5 Parkinson’s disease. This comprehensive test utilizes Next-Generation Sequencing (NGS) technology to detect specific genetic variations that increase susceptibility to early-onset Parkinson’s disease. Individuals with family history of Parkinson’s, early-onset movement disorders, or unexplained neurological symptoms should consider this test. The test provides crucial information for early intervention, personalized treatment planning, and informed family decisions. Results are delivered within 3-4 weeks using blood, extracted DNA, or FTA card samples. The test costs $500 USD and requires genetic counseling and clinical history documentation prior to testing.

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UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test

Comprehensive Genetic Testing for Hereditary Parkinson’s Disease

The UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations associated with familial Parkinson’s disease. This advanced genetic screening utilizes cutting-edge Next-Generation Sequencing technology to analyze the UCHL1 gene, which plays a critical role in protein degradation pathways within brain cells. Understanding your genetic predisposition to PARK5 Parkinson’s disease empowers individuals and families with valuable insights for proactive healthcare management.

What Does This Test Measure and Detect?

This comprehensive genetic test specifically targets the UCHL1 (Ubiquitin C-terminal Hydrolase L1) gene, which is directly linked to PARK5 Parkinson’s disease. The test identifies:

  • Pathogenic mutations in the UCHL1 gene coding regions
  • Specific genetic variants associated with early-onset Parkinson’s disease
  • Inheritance patterns of PARK5 Parkinson’s disease
  • Risk assessment for developing neurological symptoms
  • Genetic markers that influence treatment response and disease progression

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals experiencing:

  • Early-onset movement disorders or tremors
  • Family history of Parkinson’s disease across multiple generations
  • Unexplained neurological symptoms before age 50
  • Progressive motor function decline with unknown cause
  • Planning for family and concerned about hereditary neurological conditions
  • Diagnostic uncertainty in movement disorder cases

Significant Benefits of Genetic Testing

Undergoing the UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test provides numerous advantages:

  • Early Intervention Opportunities: Identify genetic risks before significant symptoms develop
  • Personalized Treatment Planning: Tailor medical approaches based on genetic profile
  • Family Planning Guidance: Make informed decisions about family health
  • Reduced Diagnostic Uncertainty: Provide clarity in complex neurological cases
  • Proactive Health Management: Implement preventive strategies and lifestyle modifications
  • Research Contribution: Advance scientific understanding of genetic Parkinson’s disease

Understanding Your Test Results

Your genetic test results will be thoroughly explained by our certified genetic counselors. Possible outcomes include:

  • Positive Result: Indicates the presence of UCHL1 gene mutation associated with PARK5 Parkinson’s disease risk
  • Negative Result: No detected mutations in the UCHL1 gene, though other genetic or environmental factors may still contribute to Parkinson’s risk
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical implications requiring further research

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps for medical management.

Test Pricing and Details

Test Feature Details
Test Name UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Nationwide Accessibility

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. Our network of certified genetic counselors and neurological specialists ensures comprehensive care regardless of your location.

Take Control of Your Neurological Health Today

Don’t let uncertainty about hereditary Parkinson’s disease affect your quality of life. Our UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test provides the clarity and information you need for informed healthcare decisions. With advanced NGS technology, expert genetic counseling, and nationwide accessibility, we make genetic testing accessible and understandable.

Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our dedicated team is ready to guide you through the testing process and help you understand your genetic health profile.

Early detection through genetic testing can make a significant difference in managing neurological health. Take the first step toward understanding your genetic predisposition to Parkinson’s disease and empower yourself with knowledge for better health outcomes.