Short Description

NGS genetic DNA test detecets for variant and mutation detection in F10 gene for Factor X deficiency

PreTest Information

Clinical History of Patient who is going for F10 Gene Factor X deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F10 Gene Factor X deficiency NGS Genetic DNA Test gene F10

Detail Description

F10 Gene Factor X Deficiency NGS Genetic DNA Test Cost INR 20,000: Symptoms and Diagnosis

Factor X deficiency, also known as Stuart-Prower factor deficiency, is a rare bleeding disorder that affects the ability of blood to clot. It is caused by mutations in the F10 gene, which provides instructions for making the Factor X protein that is essential for blood clotting.

NGS (Next Generation Sequencing) Genetic DNA Test is a cutting-edge technology that can detect mutations in the F10 gene with high accuracy and specificity. DNA Labs India offers F10 Gene Factor X Deficiency NGS Genetic DNA Test at an affordable cost of INR 20,000. This test can help diagnose Factor X deficiency and provide valuable information for treatment and management.

Symptoms of Factor X Deficiency

The symptoms of Factor X deficiency vary depending on the severity of the condition. Mild cases may not cause any symptoms, while severe cases can lead to life-threatening bleeding episodes. Some common symptoms of Factor X deficiency include:

• Easy bruising
• Nosebleeds
• Bleeding gums
• Excessive bleeding after injury or surgery
• Heavy menstrual periods
• Blood in the urine or stool
• Joint bleeding
• Internal bleeding

If you experience any of these symptoms, it is important to consult a doctor for proper diagnosis and treatment.

Diagnosis of Factor X Deficiency

Diagnosis of Factor X deficiency involves a series of tests to evaluate the clotting function of the blood. These tests may include:

• Prothrombin time (PT) test
• Activated partial thromboplastin time (aPTT) test
• Fibrinogen level test
• Factor X activity test
• Factor X antigen level test
• Genetic testing for F10 gene mutations

NGS Genetic DNA Test is a highly sensitive and specific method for detecting F10 gene mutations that cause Factor X deficiency. It can provide a definitive diagnosis and help identify carriers of the condition.

Cost and Benefits of F10 Gene Factor X Deficiency NGS Genetic DNA Test

DNA Labs India offers F10 Gene Factor X Deficiency NGS Genetic DNA Test at a cost of INR 20,000. This test provides several benefits, including:

• High accuracy and specificity
• Quick turnaround time
• Definitive diagnosis of Factor X deficiency
• Identification of carriers of the condition
• Guidance for treatment and management

The cost of the test is affordable and can provide valuable information for patients with suspected Factor X deficiency.

Conclusion

F10 Gene Factor X Deficiency NGS Genetic DNA Test is a powerful tool for diagnosing Factor X deficiency and identifying carriers of the condition. It can provide accurate and specific results at an affordable cost of INR 20,000. If you experience any symptoms of Factor X deficiency, it is important to consult a doctor and consider genetic testing for proper diagnosis and treatment.

Factor X deficiency is a rare inherited bleeding disorder characterized by insufficient levels of factor X, a protein that plays a crucial role in the blood clotting cascade. Mutations in the F10 gene, which encodes factor X, can lead to factor X deficiency.

A Next-Generation Sequencing (NGS) genetic DNA test for the F10 gene would involve sequencing the DNA of an individual to identify any variations or mutations within the gene that could be linked to factor X deficiency.

If you suspect that someone might have factor X deficiency or if there's a family history of the condition, it's important to consult with a hematologist or a healthcare professional experienced in genetics. They can guide you through the process of genetic testing, provide appropriate counseling, and help interpret the test results. Genetic testing can offer valuable insights into the genetic basis of the condition and assist in making informed medical decisions, including treatment and management strategies for bleeding disorders.