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F2 Gene Thrombophilia Due to Thrombin Defect Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The F2 Gene Thrombophilia Due to Thrombin Defect Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the F2 gene, which codes for prothrombin (also known as thrombin). Thrombin is a crucial enzyme in the blood coagulation process, and mutations in the F2 gene can lead to an increased risk of developing thrombophilia. Thrombophilia is a disorder characterized by an elevated tendency to form abnormal blood clots that can block blood vessels, posing serious health risks such as deep vein thrombosis (DVT), pulmonary embolism, and even stroke.

This test is particularly important for individuals with a family history of thrombophilia or those who have experienced unexplained thrombotic events, as it can help in the early detection and management of the condition. The process involves collecting a DNA sample, typically through a blood draw, which is then analyzed for specific genetic variations associated with the disorder.

At DNA Labs UAE, the cost for the F2 Gene Thrombophilia Due to Thrombin Defect Genetic Test is set at 4400 AED. The test is conducted with high precision and accuracy, providing crucial information that can guide healthcare providers in tailoring prevention and treatment strategies for affected individuals, ultimately helping to reduce the risk of serious thrombotic events.

Description

F2 Gene Thrombophilia due to thrombin defect Genetic Test

Test Name: F2 Gene Thrombophilia due to thrombin defect Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Vascular Diseases

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for F2 Gene Thrombophilia due to thrombin defect NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F2 Gene Thrombophilia due to thrombin defect NGS Genetic DNA Test gene F2

Test Details: F2 gene thrombophilia is a genetic condition that increases the risk of developing abnormal blood clots in veins. It is caused by a defect in the F2 gene, which provides instructions for making a protein called prothrombin. Prothrombin is a key component in the blood clotting process.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced technology to analyze multiple genes simultaneously. In the context of F2 gene thrombophilia, NGS genetic testing can be used to identify specific mutations or variations in the F2 gene that may be associated with an increased risk of abnormal blood clotting. This type of genetic testing can help healthcare professionals diagnose F2 gene thrombophilia, assess the risk of developing blood clots, and guide treatment decisions. It can also be useful for identifying family members who may be at risk and providing them with appropriate management strategies.

It is important to note that genetic testing results should always be interpreted in the context of an individual’s medical history and other risk factors. A positive result does not necessarily mean that a person will develop blood clots, and a negative result does not guarantee that a person is not at risk. Genetic testing should be done under the guidance of a healthcare professional who can provide appropriate counseling and interpretation of the results.

Test Name	F2 Gene Thrombophilia due to thrombin defect Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Vascular Diseases
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for F2 Gene Thrombophilia due to thrombin defect NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F2 Gene Thrombophilia due to thrombin defect NGS Genetic DNA Test gene F2
Test Details	F2 gene thrombophilia is a genetic condition that increases the risk of developing abnormal blood clots in veins. It is caused by a defect in the F2 gene, which provides instructions for making a protein called prothrombin. Prothrombin is a key component in the blood clotting process. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced technology to analyze multiple genes simultaneously. In the context of F2 gene thrombophilia, NGS genetic testing can be used to identify specific mutations or variations in the F2 gene that may be associated with an increased risk of abnormal blood clotting. This type of genetic testing can help healthcare professionals diagnose F2 gene thrombophilia, assess the risk of developing blood clots, and guide treatment decisions. It can also be useful for identifying family members who may be at risk and providing them with appropriate management strategies. It is important to note that genetic testing results should always be interpreted in the context of an individual’s medical history and other risk factors. A positive result does not necessarily mean that a person will develop blood clots, and a negative result does not guarantee that a person is not at risk. Genetic testing should be done under the guidance of a healthcare professional who can provide appropriate counseling and interpretation of the results.