FAH Gene Tyrosinemia type 1 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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 FAH Gene Tyrosinemia type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosinemia type 1.
Test Details
The FAH gene is associated with a rare genetic disorder called Tyrosinemia type 1. This disorder affects the body’s ability to break down the amino acid tyrosine, leading to a buildup of toxic substances in the liver, kidneys, and other organs.
NGS (Next-Generation Sequencing) is a genetic testing method that allows for the rapid and comprehensive analysis of multiple genes at once. In the case of Tyrosinemia type 1, an NGS genetic test would involve sequencing the FAH gene to identify any mutations or variations that may be causing the disorder.
This type of genetic testing can help confirm a diagnosis of Tyrosinemia type 1 and provide important information for treatment and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families at risk of having a child with Tyrosinemia type 1.
Overall, the FAH gene Tyrosinemia type 1 NGS genetic test is a valuable tool in diagnosing and managing this rare genetic disorder.
| Test Name | FAH Gene Tyrosinemia type 1 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 FAH Gene Tyrosinemia type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosinemia type 1 |
| Test Details |
The FAH gene is associated with a rare genetic disorder called Tyrosinemia type 1. This disorder affects the body’s ability to break down the amino acid tyrosine, leading to a buildup of toxic substances in the liver, kidneys, and other organs. NGS (Next-Generation Sequencing) is a genetic testing method that allows for the rapid and comprehensive analysis of multiple genes at once. In the case of Tyrosinemia type 1, an NGS genetic test would involve sequencing the FAH gene to identify any mutations or variations that may be causing the disorder. This type of genetic testing can help confirm a diagnosis of Tyrosinemia type 1 and provide important information for treatment and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families at risk of having a child with Tyrosinemia type 1. Overall, the FAH gene Tyrosinemia type 1 NGS genetic test is a valuable tool in diagnosing and managing this rare genetic disorder. |
