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F10 Gene Factor X Deficiency Genetic Test Cost

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

-21%

The F10 Gene Factor X Deficiency Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the F10 gene, which are responsible for Factor X deficiency. Factor X deficiency is a rare genetic disorder that affects the blood’s ability to clot properly, leading to an increased risk of bleeding or excessive clotting. This condition can vary in severity and may manifest as mild to severe symptoms, depending on the level of Factor X activity in the blood.

The test is crucial for individuals who have a family history of bleeding disorders or have experienced symptoms related to abnormal blood clotting. Early detection through this genetic test can aid in the proper management and treatment of the condition, potentially preventing severe complications.

The cost of the F10 Gene Factor X Deficiency Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the F10 gene. Undergoing this test at DNA Labs UAE ensures that patients receive reliable results, thanks to the laboratory’s commitment to maintaining high standards of accuracy and confidentiality in genetic testing.

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F10 Gene Factor X deficiency Genetic Test

Test Name: F10 Gene Factor X deficiency Genetic Test

Components: NGS Technology

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 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.

Test Details: F10 gene factor X deficiency NGS genetic test is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the F10 gene for any mutations or abnormalities. Factor X deficiency is a rare inherited bleeding disorder that affects the blood’s ability to clot properly. The F10 gene provides instructions for making a protein called coagulation factor X, which plays a crucial role in the blood clotting process. The NGS genetic test involves obtaining a DNA sample, usually through a blood sample or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology, which allows for the rapid and accurate analysis of the entire F10 gene. The test can identify any mutations or variations in the gene that may be associated with factor X deficiency. By identifying specific mutations or variations in the F10 gene, the test can help diagnose factor X deficiency and determine the specific genetic cause of the disorder. This information can be useful in guiding treatment decisions, predicting the risk of complications, and providing genetic counseling to affected individuals and their families. It is important to note that the F10 gene factor X deficiency NGS genetic test is a specialized test and is typically ordered by healthcare professionals with expertise in genetic testing and bleeding disorders. The test results should be interpreted in the context of a comprehensive clinical evaluation and may require further confirmatory testing.

Test Name F10 Gene Factor X 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test 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
Test Details

F10 gene factor X deficiency NGS genetic test is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the F10 gene for any mutations or abnormalities. Factor X deficiency is a rare inherited bleeding disorder that affects the blood’s ability to clot properly. The F10 gene provides instructions for making a protein called coagulation factor X, which plays a crucial role in the blood clotting process.

The NGS genetic test involves obtaining a DNA sample, usually through a blood sample or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology, which allows for the rapid and accurate analysis of the entire F10 gene. The test can identify any mutations or variations in the gene that may be associated with factor X deficiency.

By identifying specific mutations or variations in the F10 gene, the test can help diagnose factor X deficiency and determine the specific genetic cause of the disorder. This information can be useful in guiding treatment decisions, predicting the risk of complications, and providing genetic counseling to affected individuals and their families.

It is important to note that the F10 gene factor X deficiency NGS genetic test is a specialized test and is typically ordered by healthcare professionals with expertise in genetic testing and bleeding disorders. The test results should be interpreted in the context of a comprehensive clinical evaluation and may require further confirmatory testing.