FGB Gene Afibrinogenemia Congenital Genetic Test
At DNA Labs UAE, we offer the FGB Gene Afibrinogenemia Congenital Genetic Test at a cost of AED 4400.0. This test is designed to diagnose and identify the specific genetic mutations responsible for FGB gene afibrinogenemia, a rare genetic disorder characterized by the absence or severe deficiency of fibrinogen, a protein involved in blood clotting.
Test Details
The FGB Gene Afibrinogenemia Congenital Genetic Test utilizes Next-Generation Sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes and the identification of genetic variations associated with the disorder. By sequencing the DNA of an individual and comparing it to a reference genome, this test can detect small changes, such as point mutations or small insertions or deletions, as well as larger structural variations in the FGB gene.
Components and Price
The FGB Gene Afibrinogenemia Congenital Genetic Test is priced at AED 4400.0. The sample condition required for the test can be either blood, extracted DNA, or one drop of blood on an FTA Card.
Report Delivery
The report for the FGB Gene Afibrinogenemia Congenital Genetic Test is typically delivered within 3 to 4 weeks.
Test Type and Department
The FGB Gene Afibrinogenemia Congenital Genetic Test falls under the category of Hematology tests and is conducted by our experienced Hematologist in the Genetics department.
Pre Test Information
Prior to undergoing the FGB Gene Afibrinogenemia Congenital Genetic Test, it is important 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 FGB Gene Afibrinogenemia, congenital NGS Genetic DNA Test gene FGB.
Significance of FGB Gene Afibrinogenemia Congenital Genetic Test
By identifying the specific genetic mutations causing FGB gene afibrinogenemia, the FGB Gene Afibrinogenemia Congenital Genetic Test provides a definitive diagnosis for individuals with this condition. This information can be utilized for genetic counseling, family planning, and potentially for the development of targeted treatments in the future.
| Test Name | FGB 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 FGB Gene Afibrinogenemia, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGB Gene Afibrinogenemia, congenital NGS Genetic DNA Test gene FGB |
| Test Details | FGB gene afibrinogenemia is a rare genetic disorder characterized by the absence or severe deficiency of fibrinogen, a protein involved in blood clotting. This condition is caused by mutations in the FGB gene, which provides instructions for making one of the three protein chains that make up fibrinogen. Next-generation sequencing (NGS) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic variations that may be associated with a particular disorder. In the case of FGB gene afibrinogenemia, NGS genetic testing can be used to identify mutations or changes in the FGB gene that are responsible for the condition. NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any differences. This allows for the detection of small changes, such as point mutations or small insertions or deletions, as well as larger structural variations in the gene. By identifying the specific genetic mutations causing FGB gene afibrinogenemia, NGS genetic testing can provide a definitive diagnosis for individuals with this condition. This information can be used for genetic counseling, family planning, and potentially for the development of targeted treatments in the future. |
