TFR2 Gene Hemochromatosis type 3 Genetic Test
Components: TFR2 Gene Hemochromatosis type 3 Genetic Test
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 TFR2 Gene Hemochromatosis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hemochromatosis type 3.
Test Details
The TFR2 gene is associated with a form of hereditary hemochromatosis known as type 3 hemochromatosis. Hemochromatosis is a condition characterized by excessive iron absorption and accumulation in the body, leading to iron overload and potential organ damage.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the case of hemochromatosis type 3, NGS genetic testing can identify mutations or variations in the TFR2 gene that may be responsible for the condition.
By detecting specific genetic changes in the TFR2 gene, NGS genetic testing can help diagnose individuals with type 3 hemochromatosis and provide information about their risk of developing iron overload and related complications. This information can be useful in managing the condition and implementing appropriate treatment strategies, such as regular blood removal (phlebotomy) to reduce iron levels.
It is important to note that NGS genetic testing for hemochromatosis type 3 should be performed and interpreted by healthcare professionals with expertise in genetic testing and counseling. They can provide accurate diagnosis, genetic counseling, and guidance on appropriate management strategies based on the test results.
| Test Name | TFR2 Gene Hemochromatosis type 3 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 TFR2 Gene Hemochromatosis type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hemochromatosis type 3 |
| Test Details |
The TFR2 gene is associated with a form of hereditary hemochromatosis known as type 3 hemochromatosis. Hemochromatosis is a condition characterized by excessive iron absorption and accumulation in the body, leading to iron overload and potential organ damage. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the case of hemochromatosis type 3, NGS genetic testing can identify mutations or variations in the TFR2 gene that may be responsible for the condition. By detecting specific genetic changes in the TFR2 gene, NGS genetic testing can help diagnose individuals with type 3 hemochromatosis and provide information about their risk of developing iron overload and related complications. This information can be useful in managing the condition and implementing appropriate treatment strategies, such as regular blood removal (phlebotomy) to reduce iron levels. It is important to note that NGS genetic testing for hemochromatosis type 3 should be performed and interpreted by healthcare professionals with expertise in genetic testing and counseling. They can provide accurate diagnosis, genetic counseling, and guidance on appropriate management strategies based on the test results. |
