WDR48 Gene SPG60 NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Spastic Paraplegia
The WDR48 Gene SPG60 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, offering precise detection of mutations responsible for hereditary spastic paraplegia type 60. This advanced testing methodology provides healthcare providers and patients with definitive genetic information crucial for accurate diagnosis and personalized treatment strategies.
What Does This Test Measure?
This sophisticated genetic test specifically targets the WDR48 gene using next-generation sequencing technology to identify pathogenic variants associated with SPG60. The test examines:
- Complete WDR48 gene sequencing for comprehensive mutation detection
- Point mutations, insertions, and deletions affecting gene function
- Genetic variations impacting protein structure and neurological function
- Inheritance patterns relevant to autosomal recessive conditions
Who Should Consider WDR48 Gene Testing?
This genetic test is particularly recommended for individuals experiencing:
- Progressive leg stiffness and muscle spasticity
- Difficulty walking or changes in gait pattern
- Family history of hereditary spastic paraplegia
- Unexplained neurological symptoms in childhood or adulthood
- Muscle weakness affecting lower extremities
- Balance and coordination challenges
Key Benefits of WDR48 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages:
- Definitive Diagnosis: Confirm or rule out SPG60 with genetic certainty
- Personalized Treatment: Guide therapeutic interventions based on genetic findings
- Family Planning: Understand inheritance risks for future generations
- Early Intervention: Enable proactive management of neurological symptoms
- Research Contribution: Support ongoing neurological genetics research
Understanding Your Test Results
Our genetic counseling team provides comprehensive interpretation of your results:
- Positive Result: Indicates presence of WDR48 gene mutation associated with SPG60
- Negative Result: Suggests absence of tested mutations but doesn’t exclude other genetic causes
- Variant of Uncertain Significance: Requires additional clinical correlation and family studies
- Carrier Status: Identifies individuals who may pass the condition to offspring
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | WDR48 Gene SPG60 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) |
Pre-Test Requirements
To ensure optimal testing outcomes, we recommend:
- Complete clinical history documentation
- Genetic counseling session prior to testing
- Family pedigree chart development
- Neurological examination findings
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. Our network of certified genetic counselors and neurological specialists ensures comprehensive care coordination.
Take Control of Your Neurological Health
Don’t let uncertainty about hereditary spastic paraplegia affect your quality of life. Our advanced WDR48 genetic testing provides the clarity needed for informed healthcare decisions. With results typically available within 3-4 weeks and comprehensive genetic counseling support, you can move forward with confidence in your diagnostic journey.
Ready to schedule your WDR48 Gene SPG60 NGS Genetic DNA Test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take the first step toward understanding your genetic health with America’s leading neurological genetics testing provider.
