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CTH Gene Cystathioninuria Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The CTH Gene Cystathioninuria Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the CTH gene, which are linked to cystathioninuria, a rare metabolic disorder. This condition is characterized by the abnormal accumulation of cystathionine in the urine due to a deficiency in the enzyme that breaks down this compound. The test is crucial for early detection, allowing for timely intervention and management of the condition to prevent potential complications.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the CTH gene to pinpoint any genetic anomalies that may contribute to cystathioninuria. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing technologies to detect mutations.

The cost of the CTH Gene Cystathioninuria Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem steep, it reflects the sophisticated technology and expertise required to accurately identify gene mutations. For individuals with a family history of cystathioninuria or related symptoms, this test provides essential genetic insights that can guide healthcare decisions and potentially improve quality of life through personalized management strategies.

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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.