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Factor V Leiden-Mutant Detection (G1691A Mutation) by Real Time PCR – Blood
Also known as: Factor V Leiden Mutant Detection (G1691A Mutation), EDTA Blood
No special precautions
Sample Type
Blood
Recommended for
Male, Female
Report
Within 24 Hours
Blood test at Home
NABL & CAP Accredited Labs
Accurate & Quality Test Reports
Trusted by Leading Doctors & Hospitals
Overview
The Factor V Leiden-Mutant Detection (G1691A Mutation) assay utilizes real-time PCR to detect the presence of the Factor V Leiden mutation, specifically the G1691A mutation, in the blood. This mutation leads to the resistance of Factor V degradation by Activated Protein C, increasing the risk of venous thrombosis. The clinical utility of this assay lies in the evaluation of patients with suspected thrombophilia, a condition predisposing individuals to abnormal blood clotting, as well as those with a family history of Factor V Leiden mutation. Additionally, the test is useful for identifying individuals with an inherited gene mutation that heightens their risk of developing blood clots, including deep venous thrombosis (DVT) and/or venous thromboembolism (VTE). By identifying the presence of the Factor V Leiden mutation, appropriate preventive measures and treatment strategies can be implemented to mitigate the risk of venous thrombotic events.
Factor V Leiden Mutant Detection (G1691A Mutation), EDTA Blood Price
Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Factor V Leiden Mutant Detection (G1691A Mutation), EDTA Blood with a clear pricing structure.
The Factor V Leiden Mutant Detection (G1691A Mutation), EDTA Blood Price in Kamothe is ₹ 6,200 .
We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.
Frequently Asked Questions
The Factor V Leiden-Mutant Detection (G1691A Mutation) assay utilizes real-time PCR to detect the presence of the Factor V Leiden mutation, specifically the G1691A mutation, in the blood
• To identify individuals with an increased risk of venous thrombosis. • To identify if a patient has an inherited gene mutation that increases their risk of developing blood clots, including deep venous thrombosis (DVT) and/or venous thromboembolism (VTE). • In patients with clinically suspected thrombophilia or a family history of the Factor V Leiden mutation.
This test is recommended if you have • Symptoms or a family history of blood clotting disorders • Symptoms suggestive of deep venous thrombosis or venous thromboembolism • A personal or family history of Factor V Leiden mutation • Certain medical conditions, such as recurrent miscarriages or unexplained thrombosis
Abnormal results, positive for the mutation, suggest an increased risk of venous thrombosis.
This test involves drawing a small sample of blood from a vein in your arm using a needle and a syringe. You may feel a slight pinch as the needle is inserted, but the procedure is generally quick and painless. The blood sample will be sent to the laboratory for analysis.
• No fasting or special dietary restrictions are necessary. • Inform your doctor about any medications you are taking. • Provide your complete medical history and any family history of blood clotting disorders. • Please reach out to your healthcare provider for any specific requirements.
• Antithrombin III Test • Protein C and Protein S Test • D-Dimer Test
Factor V Leiden Mutation Test, G1691A Mutation Test, Factor V R506Q Mutation Test
Thrombophilia refers to a tendency to develop blood clots inappropriately. It can be caused by genetic mutations, such as the Factor V Leiden mutation. Thrombophilia increases the risk of conditions like deep venous thrombosis, pulmonary embolism, and other blood clot-related disorders.
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We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.
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