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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 offered by DNA Labs UAE, aimed at detecting genetic mutations in the F2 gene. These mutations are associated with an increased risk of thrombophilia, a condition that predisposes individuals to forming abnormal blood clots. The F2 gene plays a critical role in the production of thrombin, a key enzyme in the blood clotting process. Mutations in this gene can lead to either an overactive or underactive clotting response, both of which can have significant health implications.

This test is crucial for individuals with a family history of thrombophilia or those who have experienced unexplained blood clotting events, as it can help in the early identification of genetic predispositions towards blood clot disorders. Early detection through this genetic testing allows for personalized medical management and preventive measures to reduce the risk of serious complications associated with thrombophilia, such as deep vein thrombosis, pulmonary embolism, and stroke.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the F2 Gene Thrombophilia due to Thrombin Defect Genetic Test is 4400 AED. This investment covers the collection of a DNA sample, usually through a blood draw, the laboratory analysis to identify any genetic mutations in the F2 gene, and a comprehensive report that outlines the findings and their implications for the individual’s health. Patients considering this test are advised to consult with a healthcare professional to understand its benefits and implications fully.

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F2 Gene Thrombophilia due to thrombin defect Genetic Test

Are you at risk of abnormal blood clotting? DNA Labs UAE offers the F2 Gene Thrombophilia due to thrombin defect Genetic Test to help diagnose and manage this genetic disorder. Read on to learn more about this test and its cost.

Test Details

F2 gene thrombophilia is a genetic disorder that increases the risk of abnormal blood clotting. It is caused by a defect in the F2 gene, which codes for the production of thrombin, an important enzyme involved in blood clotting.

Our F2 Gene Thrombophilia due to thrombin defect Genetic Test uses NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. This advanced sequencing technology allows us to identify any mutations or defects in the F2 gene that may be contributing to the disorder.

To perform the test, we require a DNA sample, which can be obtained through a blood sample or cheek swab. Once we have the DNA sample, we use NGS technology to sequence the F2 gene and detect any variations or mutations.

The cost of the F2 Gene Thrombophilia due to thrombin defect Genetic Test is AED 4400.0.

Symptoms and Diagnosis

Common symptoms of F2 gene thrombophilia include an increased risk of blood clots, especially in the legs or lungs. However, it is important to note that this is a rare genetic disorder, and not everyone with the F2 gene mutation will experience symptoms.

To diagnose F2 gene thrombophilia, it is essential to consult with a hematologist who specializes in hematology. A clinical history of the patient is necessary, and a genetic counseling session may be conducted to draw a pedigree chart of family members affected by F2 gene thrombophilia.

Report Delivery and Test Department

Once the DNA sample has been sequenced, the results of the F2 Gene Thrombophilia due to thrombin defect Genetic Test will be available within 3 to 4 weeks. The report will be delivered to the hematologist overseeing the test.

This test falls under the Genetics department of DNA Labs UAE and is conducted by experienced geneticists and hematologists.

Is Genetic Testing Necessary for Everyone?

It is important to note that F2 gene thrombophilia is a rare genetic disorder, and genetic testing may not be necessary for everyone. The decision to undergo genetic testing should be made in consultation with a healthcare professional who can assess the individual’s personal and family medical history and determine the appropriate course of action.

If you suspect that you or your family members may be at risk of F2 gene thrombophilia, it is recommended to consult with a hematologist and consider genetic testing to ensure early detection and proper management of the disorder.

Take control of your health and contact DNA Labs UAE today to schedule your F2 Gene Thrombophilia due to thrombin defect Genetic Test.

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 Hematology
Doctor Hematologist
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 disorder that increases the risk of abnormal blood clotting. It is caused by a defect in the F2 gene, which codes for the production of thrombin, an important enzyme involved in blood clotting.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of F2 gene thrombophilia, NGS genetic testing can be used to identify any mutations or defects in the F2 gene that may be contributing to the disorder.

The NGS genetic test for F2 gene thrombophilia involves obtaining a DNA sample, typically through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, which allows for the detection of any variations or mutations in the F2 gene. The results of the test can help diagnose F2 gene thrombophilia and guide treatment decisions.

It is important to note that F2 gene thrombophilia is a rare genetic disorder, and genetic testing may not be necessary for everyone. The decision to undergo genetic testing should be made in consultation with a healthcare professional who can assess the individual’s personal and family medical history and determine the appropriate course of action.

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