TCN2 Gene Transcobalamin II Deficiency NGS Genetic DNA Test
Comprehensive Genetic Screening for Metabolic Health
The TCN2 Gene Transcobalamin II Deficiency NGS Genetic DNA Test represents a breakthrough in precision medicine for identifying inherited metabolic disorders. This advanced diagnostic tool specifically targets the TCN2 gene, which encodes transcobalamin II – a crucial protein responsible for vitamin B12 transport throughout the body. Vitamin B12 plays an essential role in DNA synthesis, red blood cell formation, and neurological function, making proper TCN2 gene function vital for overall health and development.
What This Test Measures and Detects
Our NGS-based genetic test provides comprehensive analysis of the TCN2 gene to identify:
- Pathogenic mutations affecting transcobalamin II production
- Genetic variants that impair vitamin B12 transport and cellular uptake
- Inherited patterns of Transcobalamin II deficiency
- Risk assessment for developing related metabolic complications
- Carrier status for family planning purposes
Who Should Consider This Test
This genetic screening is particularly recommended for individuals presenting with:
- Infants and children with unexplained developmental delays
- Patients with megaloblastic anemia unresponsive to conventional treatment
- Neurological symptoms including weakness, fatigue, or cognitive impairment
- Family history of Transcobalamin II deficiency or related metabolic disorders
- Unexplained failure to thrive in infancy
- Suspected vitamin B12 metabolism disorders
Key Benefits of Genetic Testing
Early detection through our TCN2 gene test offers numerous advantages:
- Prevention of irreversible neurological damage through timely intervention
- Personalized treatment plans including appropriate vitamin B12 supplementation
- Accurate diagnosis leading to improved quality of life
- Family planning guidance and genetic counseling opportunities
- Comprehensive understanding of metabolic health status
- Peace of mind through definitive diagnostic information
Understanding Your Test Results
Our comprehensive genetic report provides clear, actionable information:
- Positive Result: Indicates presence of TCN2 gene mutations associated with Transcobalamin II deficiency. Our genetic counselors will provide detailed guidance on treatment options and management strategies.
- Negative Result: Suggests no detected mutations in the TCN2 gene, though clinical correlation with symptoms remains important.
- Variant of Uncertain Significance: Some genetic changes may require additional family studies or clinical correlation for complete interpretation.
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TCN2 Gene Transcobalamin II Deficiency NGS Genetic DNA Test | $500 USD | $700 USD |
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 state-of-the-art laboratories ensure consistent, reliable results regardless of your location.
Take Control of Your Metabolic Health Today
Don’t wait to get the answers you need for optimal health management. Our experienced genetic specialists and comprehensive testing services provide the clarity and guidance necessary for informed healthcare decisions. Early detection of Transcobalamin II deficiency can significantly impact treatment outcomes and quality of life.
Ready to schedule your genetic screening? Contact our dedicated team today at +1(267) 388-9828 or book your appointment online. Our genetic counselors are available to discuss your specific concerns and guide you through the testing process with compassion and expertise.
