WASHC5 Gene SPG8 NGS Genetic DNA Test
Comprehensive Genetic Testing for Hereditary Spastic Paraplegia
The WASHC5 Gene SPG8 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics, providing precise identification of mutations responsible for hereditary spastic paraplegia type 8 (SPG8). This advanced testing utilizes next-generation sequencing technology to deliver comprehensive analysis of the WASHC5 gene, enabling accurate diagnosis and personalized treatment planning for patients experiencing progressive neurological symptoms.
What Does This Test Measure?
This specialized genetic test specifically targets the WASHC5 gene, which encodes the WASH complex subunit 5 protein essential for proper neuronal function and intracellular transport. The test detects:
- Pathogenic variants and mutations in the WASHC5 gene
- Single nucleotide polymorphisms associated with SPG8
- Insertions, deletions, and copy number variations
- Novel genetic variants affecting protein function
- Inheritance patterns for family risk assessment
Who Should Consider WASHC5 Gene Testing?
This genetic test is recommended for individuals experiencing:
- Progressive leg stiffness and muscle spasticity
- Difficulty walking or abnormal gait patterns
- Family history of hereditary spastic paraplegia
- Unexplained neurological symptoms beginning in adulthood
- Muscle weakness in lower extremities
- Urinary urgency or bladder control issues
- Early-onset spasticity without clear cause
- Family members of diagnosed SPG8 patients
Clinical Benefits of Genetic Testing
Undergoing WASHC5 gene testing provides numerous advantages for patients and families:
- Accurate Diagnosis: Confirms or rules out SPG8 with high precision
- Early Intervention: Enables timely management strategies
- Family Planning: Provides crucial information for reproductive decisions
- Personalized Treatment: Guides targeted therapeutic approaches
- Prognostic Information: Helps predict disease progression
- Genetic Counseling: Supports informed family risk assessment
- Research Contribution: Advances understanding of neurological disorders
Understanding Your Test Results
Your WASHC5 gene test results will be thoroughly explained during your genetic counseling session. Possible outcomes include:
- Positive Result: Identifies a pathogenic mutation confirming SPG8 diagnosis
- Negative Result: No mutation detected, though other genetic causes may exist
- Variant of Uncertain Significance: Identifies genetic changes requiring further study
- Carrier Status: Determines if you carry the mutation without symptoms
Our genetic specialists will help interpret your results in the context of your clinical symptoms and family history, providing comprehensive guidance for next steps.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We provide comprehensive genetic testing services across the United States with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, and Philadelphia. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.
Take Control of Your Neurological Health
Don’t let unexplained neurological symptoms control your life. The WASHC5 Gene SPG8 NGS Genetic DNA Test provides the clarity needed for proper diagnosis and management of hereditary spastic paraplegia. Our team of neurological genetics specialists is ready to support you through every step of the testing process.
Book your WASHC5 genetic test today by calling +1(267) 388-9828 or schedule your appointment online. Take the first step toward understanding your genetic health and securing your neurological future.
