CD59 Gene Hemolytic Anemia CD59-Mediated with or without Immune-Mediated Polyneuropathy NGS Genetic DNA Test
Comprehensive Genetic Testing for CD59-Mediated Disorders
The CD59 Gene Hemolytic Anemia NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare hematological and neurological conditions. This advanced test utilizes next-generation sequencing technology to identify mutations in the CD59 gene that cause CD59-mediated hemolytic anemia, a rare inherited disorder affecting red blood cell stability and immune system regulation.
What Does This Test Measure?
This comprehensive genetic analysis specifically targets the CD59 gene, which encodes a crucial protein that protects blood cells from complement-mediated destruction. The test detects:
- Point mutations and small insertions/deletions in the CD59 gene
- Genetic variants associated with CD59-mediated hemolytic anemia
- Mutations linked to immune-mediated polyneuropathy
- Inheritance patterns for genetic counseling purposes
- Specific genetic markers that guide treatment decisions
Who Should Consider This Test?
This genetic test is recommended for individuals experiencing:
- Unexplained hemolytic anemia with negative standard workup
- Recurrent episodes of hemoglobinuria or jaundice
- Neurological symptoms including peripheral neuropathy
- Family history of CD59-related disorders
- Children with developmental delays and hematological abnormalities
- Patients with atypical response to standard anemia treatments
Clinical Symptoms and Indications
Patients may present with various symptoms including chronic fatigue, pallor, dark urine, neurological deficits, muscle weakness, and sensory disturbances. Early diagnosis through genetic testing can prevent complications and guide appropriate management strategies.
Benefits of CD59 Genetic Testing
Accurate Diagnosis and Personalized Care
Our NGS-based CD59 genetic test provides numerous clinical benefits:
- Precise Diagnosis: Eliminates diagnostic uncertainty and prevents misdiagnosis
- Family Planning: Enables informed reproductive decisions and genetic counseling
- Treatment Guidance: Helps hematologists develop targeted treatment protocols
- Prognostic Information: Provides insights into disease progression and potential complications
- Early Intervention: Facilitates timely management to prevent serious complications
Understanding Your Test Results
Interpreting Genetic Findings
Your test results will be carefully analyzed and explained by our genetic specialists:
- Positive Result: Indicates the presence of CD59 gene mutations associated with the disorder
- Negative Result: Suggests absence of known CD59 mutations but may require additional testing
- Variant of Uncertain Significance: Requires further clinical correlation and family studies
- Carrier Status: Identifies individuals who may pass the condition to offspring
All results include comprehensive interpretation and recommendations for follow-up care with hematology and neurology specialists.
Test Details and Pricing
| Test Information | Details |
|---|---|
| Test Name | CD59 Gene Hemolytic Anemia CD59-Mediated with or without Immune-Mediated Polyneuropathy 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 |
Pre-Test Requirements
Before scheduling your CD59 genetic test, please ensure:
- Complete clinical history documentation
- Genetic counseling session to create family pedigree chart
- Discussion of testing implications with healthcare provider
- Understanding of potential outcomes and their significance
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 testing for patients nationwide.
Take Control of Your Health Today
Don’t let unexplained symptoms or family history concerns go unaddressed. Our CD59 genetic test provides the answers you need for proper diagnosis and management. With our discounted price of $500 and comprehensive genetic analysis, you can make informed decisions about your healthcare journey.
Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Our team is available to answer your questions and guide you through the testing process.
Take the first step toward understanding your genetic health and receiving the specialized care you deserve. Early diagnosis through genetic testing can significantly improve outcomes and quality of life for individuals with CD59-mediated disorders.
