Wilson Disease Panel Test – Comprehensive Copper Metabolism Analysis
Understanding Wilson’s Disease and Diagnostic Importance
Wilson Disease Panel Test represents a crucial diagnostic tool for identifying Wilson’s disease, a rare autosomal recessive genetic disorder characterized by abnormal copper accumulation in vital organs. This comprehensive panel provides healthcare providers with essential data to confirm or rule out this potentially life-threatening condition that affects approximately 1 in 30,000 individuals worldwide.
The significance of early Wilson’s disease detection cannot be overstated. When left undiagnosed, copper buildup can lead to irreversible liver damage, neurological deterioration, and psychiatric manifestations. Our advanced testing methodology ensures accurate assessment of copper metabolism, enabling timely intervention and appropriate treatment strategies.
What the Wilson Disease Panel Measures
Our comprehensive Wilson Disease Panel evaluates multiple biomarkers essential for copper metabolism assessment:
Core Test Components
- Complete Blood Count (CBC): Assesses overall blood health and detects potential hemolytic anemia
- Liver Function Tests (LFT): Evaluates liver enzyme levels and bilirubin to detect hepatic involvement
- Ceruloplasmin Level: Measures the primary copper-carrying protein in blood, typically reduced in Wilson’s disease
- Serum Copper: Quantifies circulating copper levels in the bloodstream
- 24-Hour Urine Copper: Assesses copper excretion capacity, a critical diagnostic parameter
Who Should Consider Wilson Disease Testing
This comprehensive panel is recommended for individuals presenting with symptoms suggestive of copper metabolism disorders:
Clinical Indications and Symptoms
- Unexplained liver enzyme elevations or abnormal liver function tests
- Neurological symptoms including tremors, dystonia, or coordination difficulties
- Psychiatric manifestations such as depression, personality changes, or cognitive decline
- Kayser-Fleischer rings observed during ophthalmological examination
- Family history of Wilson’s disease or unexplained liver conditions
- Young adults (typically 5-35 years) with unexplained hepatic or neurological symptoms
Benefits of Wilson Disease Panel Testing
Early detection through comprehensive Wilson Disease Panel testing offers numerous advantages:
Clinical Benefits
- Early Intervention: Enables prompt treatment initiation before irreversible organ damage occurs
- Accurate Diagnosis: Provides comprehensive data for definitive Wilson’s disease confirmation
- Treatment Monitoring: Establishes baseline values for ongoing therapeutic management
- Family Screening: Identifies at-risk family members for preventive measures
- Differential Diagnosis: Helps distinguish Wilson’s disease from other hepatic and neurological conditions
Understanding Your Test Results
Interpreting Wilson Disease Panel results requires professional medical expertise, but general guidance includes:
Result Interpretation Framework
- Ceruloplasmin Levels: Typically below 20 mg/dL in Wilson’s disease patients
- 24-Hour Urine Copper: Usually exceeds 100 μg/24 hours in symptomatic patients
- Serum Copper: May be decreased due to low ceruloplasmin levels
- Liver Enzymes: Elevated levels indicate hepatic involvement and potential damage
- Complete Pattern Analysis: Diagnosis relies on combined interpretation of all parameters
It’s crucial to consult with your healthcare provider for comprehensive result interpretation and personalized treatment recommendations based on your specific clinical presentation.
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $138 |
| Regular Price | $200 |
Testing Logistics
- Turnaround Time: Samples accepted Monday through Saturday by 6 PM; Reports delivered next day
- Sample Requirements: Comprehensive specimen collection including whole blood, serum, and 24-hour urine samples
- Analytical Methods: Advanced techniques including Spectrophotometry, Nephelometry, Electrical Impedance, VCS, and ICP-MS
Nationwide Testing Availability
GGC DNA maintains comprehensive testing facilities across the United States, with convenient locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures accessible Wilson Disease Panel testing regardless of your location.
Take Action for Your Health
Don’t let uncertainty about copper metabolism disorders compromise your health. Our Wilson Disease Panel provides the comprehensive assessment needed for accurate diagnosis and effective treatment planning. Early detection can prevent serious complications and improve long-term outcomes.
Ready to schedule your Wilson Disease Panel Test? Contact our dedicated healthcare team today at +1(267) 388-9828 or book your appointment online. Our specialists are available to answer your questions and guide you through the testing process.
Take the first step toward understanding your copper metabolism health with GGC DNA’s advanced Wilson Disease Panel testing. Your journey to better health begins with accurate diagnosis.
