F2 Gene Factor II deficiency Genetic Test
Cost: AED 4400.0
Symptoms, Diagnosis, and Test Details
Factor II deficiency, also known as prothrombin deficiency, is a rare bleeding disorder caused by a mutation in the F2 gene. This gene provides instructions for making a protein called prothrombin, which plays a crucial role in the blood clotting process.
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 Factor II deficiency, NGS genetic testing can identify mutations or variations in the F2 gene that may be responsible for the disorder.
NGS genetic testing can provide valuable information about an individual’s genetic makeup, including the presence of mutations in the F2 gene. This information can help healthcare professionals diagnose Factor II deficiency and develop appropriate treatment plans.
It is important to note that genetic testing for Factor II deficiency is typically performed in individuals with a suspected bleeding disorder or a family history of the condition. A healthcare professional, such as a genetic counselor or hematologist, can help determine if genetic testing is appropriate and provide guidance on the implications of the test results.
Test Components and Price
- Test Name: F2 Gene Factor II deficiency Genetic Test
- Components: Blood or Extracted DNA or One drop Blood on FTA Card
- Price: AED 4400.0
Report Delivery and Method
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
Test Type and Doctor
- Test Type: Vascular Diseases
- Doctor: General Physician
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for F2 Gene Factor II deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F2 Gene Factor II deficiency NGS Genetic DNA Test gene F2.
| Test Name | F2 Gene Factor II deficiency 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 Factor II deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F2 Gene Factor II deficiency NGS Genetic DNA Test gene F2 |
| Test Details | Factor II deficiency, also known as prothrombin deficiency, is a rare bleeding disorder caused by a mutation in the F2 gene. This gene provides instructions for making a protein called prothrombin, which plays a crucial role in the blood clotting process. 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 Factor II deficiency, NGS genetic testing can identify mutations or variations in the F2 gene that may be responsible for the disorder. NGS genetic testing can provide valuable information about an individual’s genetic makeup, including the presence of mutations in the F2 gene. This information can help healthcare professionals diagnose Factor II deficiency and develop appropriate treatment plans. It is important to note that genetic testing for Factor II deficiency is typically performed in individuals with a suspected bleeding disorder or a family history of the condition. A healthcare professional, such as a genetic counselor or hematologist, can help determine if genetic testing is appropriate and provide guidance on the implications of the test results. |
