Short Description

NGS genetic DNA test detecets for variant and mutation detection in F2 gene for Dysprothrombinemia

PreTest Information

Clinical History of Patient who is going for F2 Gene Dysprothrombinemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F2 Gene Dysprothrombinemia NGS Genetic DNA Test gene F2

Detail Description

F2 Gene Dysprothrombinemia NGS Genetic DNA Test

Dysprothrombinemia is a genetic disorder that causes abnormalities in the protein responsible for blood clotting, known as prothrombin. The F2 gene encodes for prothrombin, and mutations in this gene can result in F2 gene dysprothrombinemia. This disorder can increase the risk of developing blood clots, which can lead to serious health issues such as stroke and heart attacks.

Fortunately, with advances in genetic testing, it is now possible to detect mutations in the F2 gene that cause dysprothrombinemia. NGS (Next Generation Sequencing) technology is used to analyze the entire F2 gene and identify any mutations that may be present. This can help to diagnose dysprothrombinemia and provide appropriate treatment options.

Symptoms of F2 Gene Dysprothrombinemia

The symptoms of F2 gene dysprothrombinemia can vary depending on the severity of the mutation. Some individuals may experience no symptoms at all, while others may have a higher risk of blood clots. Common symptoms include:

• Abnormal blood clotting
• Deep vein thrombosis (DVT)
• Pulmonary embolism
• Stroke
• Heart attack

If you experience any of these symptoms or have a family history of dysprothrombinemia, it is important to speak with a healthcare professional about genetic testing.

Diagnosis of F2 Gene Dysprothrombinemia

Diagnosing F2 gene dysprothrombinemia involves a combination of genetic testing and medical history evaluation. NGS genetic testing can detect mutations in the F2 gene that may be responsible for dysprothrombinemia. A healthcare professional may also ask about any symptoms you are experiencing, as well as your family history of blood clotting disorders.

NGS Genetic DNA Test Cost

The cost of NGS genetic testing for F2 gene dysprothrombinemia can vary depending on the laboratory performing the test. At DNA Labs India, the cost of this test is INR 20,000. This includes the cost of the test, as well as genetic counseling to help you understand your results and any implications they may have for your health.

Conclusion

F2 gene dysprothrombinemia is a genetic disorder that can increase the risk of blood clots and lead to serious health complications. NGS genetic testing is a powerful tool that can help to diagnose this disorder and provide appropriate treatment options. If you are experiencing any symptoms or have a family history of dysprothrombinemia, it is important to speak with a healthcare professional about genetic testing.

At DNA Labs India, we offer affordable and accurate NGS genetic testing for F2 gene dysprothrombinemia. Contact us today to learn more about this test and how it can benefit your health.