CR1 Gene CR1 Deficiency NGS Genetic DNA Test
Comprehensive Genetic Testing for Neurological Disorders
The CR1 Gene CR1 Deficiency NGS Genetic DNA Test represents a cutting-edge approach to diagnosing genetic conditions affecting the complement system and neurological function. This specialized test examines the CR1 gene, which encodes complement receptor type 1, a crucial protein involved in immune regulation and cellular communication within the nervous system.
What Does This Test Measure?
Our advanced NGS (Next-Generation Sequencing) technology provides comprehensive analysis of the CR1 gene to identify:
- Point mutations and single nucleotide variations
- Insertions and deletions within the gene sequence
- Copy number variations affecting CR1 expression
- Regulatory region mutations impacting gene function
- Pathogenic variants associated with CR1 deficiency disorders
Who Should Consider This Test?
This genetic test is particularly recommended for individuals experiencing:
- Unexplained neurological symptoms including cognitive decline
- Recurrent infections or immune system abnormalities
- Family history of CR1 deficiency or complement system disorders
- Autoimmune conditions with neurological manifestations
- Unexplained developmental delays in children
- Multiple family members with similar neurological symptoms
Clinical Benefits of CR1 Gene Testing
Undergoing CR1 gene deficiency testing provides numerous clinical advantages:
- Accurate Diagnosis: Precise identification of genetic mutations causing symptoms
- Personalized Treatment: Targeted therapeutic approaches based on genetic findings
- Family Planning: Informed reproductive decisions and genetic counseling
- Early Intervention: Proactive management of potential complications
- Risk Assessment: Understanding inheritance patterns for family members
Understanding Your Test Results
Our comprehensive genetic report provides detailed interpretation of your results:
- Positive Result: Identifies specific CR1 gene mutations requiring medical management
- Negative Result: No pathogenic variants detected in the CR1 gene
- Variant of Uncertain Significance: Genetic changes requiring further clinical correlation
- Carrier Status: Identification of individuals carrying one copy of mutated gene
All results are accompanied by detailed explanations and recommendations for next steps, including consultation with our genetic specialists.
Test Pricing and Details
| Test Component | Details |
|---|---|
| Test Name | CR1 Gene CR1 Deficiency 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 Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.
Pre-Test Requirements
Before scheduling your CR1 gene 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 results and their significance
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic conditions affect your quality of life. Our CR1 Gene CR1 Deficiency NGS Genetic DNA Test provides the clarity needed for informed healthcare decisions. With our discounted price of $500 USD and comprehensive nationwide coverage, accessing advanced genetic testing has never been more convenient.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or book your test online. Our genetic specialists are ready to assist you with personalized guidance and support throughout your testing journey.
