F11 Gene Factor XI Deficiency Genetic Test
Welcome to DNA Labs UAE, where we offer the F11 Gene Factor XI Deficiency Genetic Test. This diagnostic test uses next-generation sequencing (NGS) technology to identify mutations or variations in the F11 gene that may be responsible for factor XI deficiency.
Test Components and Price
The F11 Gene Factor XI Deficiency Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.
Report Delivery
The test results will be delivered within 3 to 4 weeks.
Method and Test Type
The F11 Gene Factor XI Deficiency Genetic Test utilizes NGS technology. It falls under the categories of Hepatology, Nephrology, and Endocrinology Disorders.
Doctor and Test Department
This test is recommended by General Physicians and falls under the Genetics department.
Pre-Test Information
Before undergoing the F11 Gene Factor XI Deficiency Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by F11 Gene Factor XI Deficiency.
Test Details
Factor XI deficiency is a rare inherited bleeding disorder characterized by a deficiency of clotting factor XI, which plays a crucial role in the blood clotting process. The F11 Gene Factor XI Deficiency Genetic Test analyzes the entire coding region of the F11 gene, including exons and introns, to identify any genetic changes that may affect the production or function of factor XI.
This comprehensive test can detect various types of mutations, such as point mutations, insertions, deletions, and rearrangements. It is typically performed on a blood sample, with the DNA extracted and sequenced using NGS technology. The resulting sequence data is then compared to a reference sequence to identify any genetic variations.
The test results can be interpreted by clinicians and geneticists to determine if a patient has a mutation in the F11 gene associated with factor XI deficiency. It helps confirm a diagnosis of factor XI deficiency in individuals with clinical symptoms and can be used for carrier testing in individuals with a family history of the condition. It is also applicable for prenatal testing in couples at risk of having a child with factor XI deficiency.
The F11 Gene Factor XI Deficiency Genetic Test provides valuable information for genetic counseling, family planning, and guiding appropriate management and treatment strategies for individuals with factor XI deficiency.
| Test Name | F11 Gene Factor XI 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 | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for F11 Gene Factor XI deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F11 Gene Factor XI deficiency NGS Genetic DNA Test gene F11 |
| Test Details |
F11 gene factor XI deficiency NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to identify mutations or variations in the F11 gene that may be responsible for factor XI deficiency. Factor XI deficiency is a rare inherited bleeding disorder characterized by a deficiency of clotting factor XI, which is involved in the blood clotting process. The NGS genetic test analyzes the entire coding region of the F11 gene, including its exons and introns, to identify any genetic changes that may affect the production or function of factor XI. This test can detect various types of mutations, including point mutations, insertions, deletions, and rearrangements, providing a comprehensive analysis of the F11 gene. The test is typically performed on a blood sample, and the DNA is extracted and sequenced using NGS technology. The resulting sequence data is then compared to a reference sequence to identify any genetic variations. Clinicians and geneticists can interpret the test results to determine if a patient has a mutation in the F11 gene that is associated with factor XI deficiency. The F11 gene factor XI deficiency NGS genetic test can help confirm a diagnosis of factor XI deficiency in individuals with clinical symptoms of the disorder. It can also be used for carrier testing in individuals with a family history of factor XI deficiency or for prenatal testing in couples at risk of having a child with the condition. The test results can provide valuable information for genetic counseling and family planning, as well as guide appropriate management and treatment strategies for individuals with factor XI deficiency. |
