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Factor V Leiden Mutation Analysis Test

Original price was: $262.Current price is: $188.

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The Factor V Leiden Mutation Analysis Test is a comprehensive genetic screening that identifies inherited blood clotting disorders. This advanced molecular diagnostic test detects mutations in the Factor V Leiden gene, Prothrombin gene, and MTHFR gene that increase thrombosis risk. Using Real-Time PCR technology, the test provides accurate results for individuals with personal or family history of blood clots, recurrent miscarriages, or unexplained thrombotic events. Early detection allows for proactive management through anticoagulant therapy and lifestyle modifications. Available for $188 USD, this test is essential for anyone concerned about inherited thrombophilia conditions. Our nationwide network ensures convenient testing across major US cities with rapid turnaround times.

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Factor V Leiden Mutation Analysis Test

Understanding Factor V Leiden Mutation Analysis

The Factor V Leiden Mutation Analysis Test represents a breakthrough in genetic thrombophilia screening, providing comprehensive insights into inherited blood clotting disorders. This sophisticated molecular diagnostic examination identifies specific genetic mutations that significantly increase an individual’s susceptibility to developing dangerous blood clots. As one of the most common inherited thrombophilia conditions, Factor V Leiden mutation affects approximately 5% of the Caucasian population and requires precise detection for effective clinical management.

What This Advanced Test Measures

Our comprehensive genetic panel evaluates three critical mutations associated with thrombotic risk:

  • Factor V Leiden Mutation: The most prevalent inherited thrombophilia, this mutation causes resistance to activated protein C, leading to excessive blood clotting
  • Prothrombin Gene Mutation (G20210A): This genetic variation increases prothrombin levels in the blood, elevating thrombosis risk
  • MTHFR Gene Mutation: Affects homocysteine metabolism, contributing to vascular complications and thrombotic events

Who Should Consider This Genetic Screening?

This test is particularly recommended for individuals experiencing:

  • Unexplained deep vein thrombosis (DVT) or pulmonary embolism (PE)
  • Recurrent pregnancy loss or multiple miscarriages
  • Family history of blood clotting disorders
  • Thrombotic events at a young age (under 50 years)
  • Blood clots in unusual locations (cerebral, mesenteric, or portal veins)
  • Women considering hormonal contraception or hormone replacement therapy
  • Patients with arterial thrombosis without traditional risk factors

Clinical Significance and Benefits

Early detection through Factor V Leiden Mutation Analysis provides numerous advantages:

  • Proactive Risk Management: Identifies genetic predisposition before thrombotic events occur
  • Personalized Treatment Planning: Guides appropriate anticoagulant therapy decisions
  • Family Screening Opportunities: Enables testing of relatives when a mutation is identified
  • Reproductive Health Guidance: Assists in managing pregnancy-related thrombotic risks
  • Lifestyle Modification Insights: Informs decisions about travel, surgery, and medication use

Understanding Your Test Results

Our comprehensive reporting provides clear interpretation of your genetic findings:

  • Negative Result: No detected mutations – indicates standard thrombotic risk profile
  • Heterozygous Mutation: One copy of mutated gene – moderate increased thrombosis risk
  • Homozygous Mutation: Two copies of mutated gene – significantly elevated thrombosis risk
  • Compound Heterozygosity: Multiple different mutations – requires specialized management

All results include detailed clinical recommendations and are reviewed by our board-certified hematologists to ensure accurate interpretation and appropriate follow-up care planning.

Test Pricing and Availability

Test Component Price Type Amount (USD)
Factor V Leiden Mutation Analysis Discount Price $188
Factor V Leiden Mutation Analysis Regular Price $262

Nationwide Testing Accessibility

We maintain comprehensive testing facilities across the United States, with convenient locations in 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 molecular diagnostics laboratories ensure consistent, reliable results regardless of testing location.

Advanced Testing Methodology

Our Factor V Leiden Mutation Analysis employs cutting-edge Real-Time PCR technology, providing exceptional accuracy and sensitivity in genetic mutation detection. This methodology offers:

  • Superior detection sensitivity exceeding 99%
  • Rapid turnaround with results available within specified timeframes
  • Minimal sample requirements with 3 mL whole blood collection
  • No special patient preparation needed before testing
  • Comprehensive quality control measures at every processing stage

Take Control of Your Thrombotic Health

Understanding your genetic predisposition to blood clotting disorders empowers you to make informed healthcare decisions. Our Factor V Leiden Mutation Analysis provides the critical information needed to develop personalized prevention strategies and appropriate medical interventions. Don’t wait for a thrombotic event to discover your genetic risk profile.

Schedule your comprehensive genetic thrombophilia screening today by calling our dedicated healthcare line at +1(267) 388-9828 or book your appointment online. Our genetic counseling team is available to discuss your results and provide personalized recommendations based on your genetic profile.