FGG Gene Afibrinogenemia congenital Genetic Test
Test Name: FGG Gene Afibrinogenemia congenital Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 FGG Gene Afibrinogenemia, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGG Gene Afibrinogenemia, congenital NGS Genetic DNA Test gene FGG
Test Details: FGG gene afibrinogenemia is a rare genetic disorder characterized by a deficiency or complete absence of fibrinogen, a protein necessary for blood clotting. This condition is caused by mutations in the FGG gene, which provides instructions for making one of the three subunits of fibrinogen.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of genetic mutations associated with various disorders. In the case of FGG gene afibrinogenemia, NGS genetic testing can be used to identify specific mutations within the FGG gene that are responsible for the condition.
NGS genetic testing involves the sequencing of DNA or RNA samples obtained from the individual being tested. This sequencing technique can provide a comprehensive analysis of the genetic material, allowing for the identification of mutations or variants in the FGG gene that may be causing afibrinogenemia.
By performing NGS genetic testing for FGG gene afibrinogenemia, healthcare professionals can provide a definitive diagnosis for individuals suspected of having this condition. This can help guide appropriate treatment strategies and provide important information for genetic counseling and family planning.
| Test Name | FGG Gene Afibrinogenemia congenital 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 FGG Gene Afibrinogenemia, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGG Gene Afibrinogenemia, congenital NGS Genetic DNA Test gene FGG |
| Test Details | FGG gene afibrinogenemia is a rare genetic disorder characterized by a deficiency or complete absence of fibrinogen, a protein necessary for blood clotting. This condition is caused by mutations in the FGG gene, which provides instructions for making one of the three subunits of fibrinogen. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the detection of genetic mutations associated with various disorders. In the case of FGG gene afibrinogenemia, NGS genetic testing can be used to identify specific mutations within the FGG gene that are responsible for the condition. NGS genetic testing involves the sequencing of DNA or RNA samples obtained from the individual being tested. This sequencing technique can provide a comprehensive analysis of the genetic material, allowing for the identification of mutations or variants in the FGG gene that may be causing afibrinogenemia. By performing NGS genetic testing for FGG gene afibrinogenemia, healthcare professionals can provide a definitive diagnosis for individuals suspected of having this condition. This can help guide appropriate treatment strategies and provide important information for genetic counseling and family planning. |
