F5 Gene Factor V Deficiency NGS Genetic DNA Test
Comprehensive Genetic Analysis for Bleeding Disorders
The F5 Gene Factor V Deficiency NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for bleeding disorders. Factor V deficiency, also known as Owren’s disease or parahemophilia, is a rare autosomal recessive bleeding disorder affecting the coagulation cascade. This sophisticated test utilizes cutting-edge Next-Generation Sequencing technology to provide comprehensive analysis of the F5 gene, enabling precise identification of mutations responsible for this inherited condition.
What Does This Test Measure?
This advanced genetic test specifically targets and sequences the entire F5 gene to detect mutations that cause Factor V deficiency. The test examines:
- Complete F5 gene sequencing for point mutations and small insertions/deletions
- Detection of known pathogenic variants associated with Factor V deficiency
- Identification of novel mutations affecting Factor V protein function
- Analysis of genetic variations impacting coagulation factor production
Who Should Consider This Test?
This genetic test is recommended for individuals experiencing:
- Unexplained bleeding episodes or easy bruising
- Prolonged bleeding after minor injuries or surgeries
- Abnormal coagulation test results (prolonged PT and PTT)
- Family history of bleeding disorders or Factor V deficiency
- Women with heavy menstrual bleeding or postpartum hemorrhage
- Individuals with suspected inherited coagulation disorders
Clinical Benefits of Testing
Undergoing the F5 Gene Factor V Deficiency test provides numerous clinical advantages:
- Accurate diagnosis and differentiation from other bleeding disorders
- Personalized treatment planning and bleeding risk assessment
- Genetic counseling for family planning decisions
- Improved surgical and procedural safety planning
- Early intervention strategies for affected individuals
- Comprehensive understanding of inheritance patterns
Understanding Your Test Results
Your genetic test results will provide clear information about your F5 gene status:
- Normal Result: No pathogenic mutations detected in the F5 gene
- Carrier Status: One mutated copy detected – typically asymptomatic but can pass to offspring
- Affected Status: Two mutated copies detected – indicates Factor V deficiency
- Variant of Uncertain Significance: Genetic change detected with unknown clinical impact
All results include detailed interpretation by our genetic specialists and recommendations for follow-up care.
Test Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| F5 Gene Factor V Deficiency NGS Genetic DNA Test | $500 USD | $700 USD |
Nationwide Testing Availability
We have comprehensive testing facilities across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.
Take Control of Your Genetic Health
Understanding your genetic predisposition to bleeding disorders can significantly impact your healthcare decisions and quality of life. The F5 Gene Factor V Deficiency NGS Genetic DNA Test provides the clarity needed for informed medical management and family planning.
Ready to schedule your test? Contact our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take the first step toward comprehensive genetic understanding and personalized healthcare.
