CTH Gene Cystathioninuria Genetic Test
At DNA Labs UAE, we offer the CTH Gene Cystathioninuria Genetic Test at a cost of AED 4400.0. This test is designed to analyze the CTH gene for mutations associated with cystathioninuria, an inherited metabolic disorder.
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
Prior to undergoing the CTH Gene Cystathioninuria Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Cystathioninuria.
Test Details
The CTH gene cystathioninuria NGS genetic test is a type of genetic test that analyzes the CTH gene for mutations associated with cystathioninuria. Cystathioninuria is an inherited metabolic disorder characterized by elevated levels of cystathionine in the urine.
The CTH gene provides instructions for producing an enzyme called cystathionine gamma-lyase, which is involved in the breakdown of the amino acid methionine. Mutations in the CTH gene can lead to reduced or absent enzyme activity, causing the accumulation of cystathionine.
NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the context of the CTH gene cystathioninuria test, NGS can be used to identify specific mutations or variants in the CTH gene that are associated with cystathioninuria.
This genetic test can be helpful in diagnosing cystathioninuria, as well as identifying carriers of the condition. It may also be used for genetic counseling and family planning purposes.
Test Name | CTH Gene Cystathioninuria 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 CTH Gene Cystathioninuria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Cystathioninuria |
Test Details |
CTH gene cystathioninuria NGS genetic test is a type of genetic test that analyzes the CTH gene for mutations associated with cystathioninuria. Cystathioninuria is an inherited metabolic disorder characterized by elevated levels of cystathionine in the urine. The CTH gene provides instructions for producing an enzyme called cystathionine gamma-lyase, which is involved in the breakdown of the amino acid methionine. Mutations in the CTH gene can lead to reduced or absent enzyme activity, causing the accumulation of cystathionine. NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the context of the CTH gene cystathioninuria test, NGS can be used to identify specific mutations or variants in the CTH gene that are associated with cystathioninuria. This genetic test can be helpful in diagnosing cystathioninuria, as well as identifying carriers of the condition. It may also be used for genetic counseling and family planning purposes. |