F2 Gene Factor II deficiency Genetic Test
At DNA Labs UAE, we offer the F2 Gene Factor II deficiency Genetic Test to provide valuable information about an individual’s genetic predisposition to abnormal blood clotting. This test can help in the diagnosis and management of the condition, as well as in assessing the risk of developing complications such as deep vein thrombosis or pulmonary embolism.
Test Details
The F2 gene, also known as the Factor II gene, encodes for a protein called prothrombin. Prothrombin is a precursor protein that plays a crucial role in the blood clotting process. Mutations in the F2 gene can lead to a deficiency or dysfunction of prothrombin, which can result in abnormal blood clotting.
Our F2 Gene Factor II deficiency Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of an individual’s genes. This technique allows for the identification of specific mutations or variants in the F2 gene that may be associated with Factor II deficiency.
Test Components and Price
The cost of the F2 Gene Factor II deficiency Genetic Test is AED 4400.0. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA card. The report will be delivered within 3 to 4 weeks.
Test Type and Method
The F2 Gene Factor II deficiency Genetic Test falls under the category of Metabolic Disorders. The method used for this test is NGS (Next-Generation Sequencing) technology.
Test Department and Doctor
The F2 Gene Factor II deficiency Genetic Test is conducted by our Genetics department, under the supervision of a General Physician.
Pre Test Information
Prior to undergoing the F2 Gene Factor II deficiency Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with Factor II deficiency.
Test Process
The NGS genetic testing for F2 Gene Factor II deficiency involves obtaining a DNA sample, usually through a blood or saliva sample. The DNA is then sequenced using NGS technology, allowing for the identification of specific variations or mutations in the F2 gene.
Benefits of the Test
The results of the F2 Gene Factor II deficiency Genetic Test can provide valuable information for healthcare providers. It can help determine the appropriate treatment and management strategies for individuals with Factor II deficiency. The test can also be used for genetic counseling and family planning purposes, as it can identify if an individual carries a mutation that can be passed on to their children.
Important Note
It is crucial to conduct genetic testing for Factor II deficiency under the guidance of a healthcare professional or genetic counselor. They can interpret the results and provide appropriate recommendations based on an individual’s specific circumstances.
| 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 | Metabolic Disorders |
| 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 Factor II deficiency |
| Test Details |
F2 gene, also known as the Factor II gene, encodes for a protein called prothrombin. Prothrombin is a precursor protein that plays a crucial role in the blood clotting process. Mutations in the F2 gene can lead to a deficiency or dysfunction of prothrombin, which can result in abnormal blood clotting. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It allows for the identification of specific mutations or variants in the F2 gene that may be associated with Factor II deficiency. NGS genetic testing for F2 gene Factor II deficiency can provide valuable information about an individual’s genetic predisposition to abnormal blood clotting. This information can help in the diagnosis and management of the condition, as well as in assessing the risk of developing complications such as deep vein thrombosis or pulmonary embolism. The NGS genetic test involves obtaining a DNA sample, usually through a blood or saliva sample, from the individual. The DNA is then sequenced using NGS technology, which allows for the identification of specific variations or mutations in the F2 gene. The results of the NGS genetic test can help healthcare providers determine the appropriate treatment and management strategies for individuals with Factor II deficiency. It can also be used for genetic counseling and family planning purposes, as the test can identify if an individual carries a mutation that can be passed on to their children. It is important to note that genetic testing for Factor II deficiency should be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on an individual’s specific circumstances. |
