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TAT Gene Tyrosinemia type 2 Genetic Test

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

-21%

The TAT Gene Tyrosinemia Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the TAT gene, which are responsible for Tyrosinemia type 2, a rare metabolic disorder. This condition is characterized by elevated levels of tyrosine in the blood, leading to issues such as skin lesions, eye problems, and, in some cases, intellectual disability. The test, priced at 4400 AED, involves analyzing the patient’s DNA to identify any genetic alterations in the TAT gene, providing crucial information for accurate diagnosis and enabling targeted treatment approaches. By identifying the specific mutations causing Tyrosinemia type 2, healthcare providers can offer personalized management plans to mitigate the symptoms and improve the quality of life for affected individuals.

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TAT Gene Tyrosinemia type 2 Genetic Test

Test Name: TAT Gene Tyrosinemia type 2 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for TAT Gene Tyrosinemia type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosinemia type 2.

Test Details

The TAT (Tyrosine aminotransferase) gene is associated with a rare genetic disorder called Tyrosinemia type 2. This disorder is characterized by the deficiency of the enzyme tyrosine aminotransferase, which is involved in the breakdown of the amino acid tyrosine. As a result, tyrosine and its byproducts accumulate in the body, leading to various symptoms and complications.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the identification of specific genetic variations or mutations that may be associated with a particular disorder, such as Tyrosinemia type 2. NGS can provide a comprehensive analysis of the entire TAT gene, allowing for the detection of any mutations or variations that may be present.

NGS genetic testing for Tyrosinemia type 2 can be used to confirm a diagnosis in individuals suspected of having the disorder. It can also be used for carrier testing in individuals with a family history of Tyrosinemia type 2 or for prenatal testing in couples at risk of having a child with the disorder. The results of the test can help guide medical management and treatment decisions for affected individuals and their families.

Test Name TAT Gene Tyrosinemia type 2 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 TAT Gene Tyrosinemia type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosinemia type 2
Test Details

TAT (Tyrosine aminotransferase) gene is associated with a rare genetic disorder called Tyrosinemia type 2. This disorder is characterized by the deficiency of the enzyme tyrosine aminotransferase, which is involved in the breakdown of the amino acid tyrosine. As a result, tyrosine and its byproducts accumulate in the body, leading to various symptoms and complications.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the identification of specific genetic variations or mutations that may be associated with a particular disorder, such as Tyrosinemia type 2. NGS can provide a comprehensive analysis of the entire TAT gene, allowing for the detection of any mutations or variations that may be present.

NGS genetic testing for Tyrosinemia type 2 can be used to confirm a diagnosis in individuals suspected of having the disorder. It can also be used for carrier testing in individuals with a family history of Tyrosinemia type 2 or for prenatal testing in couples at risk of having a child with the disorder. The results of the test can help guide medical management and treatment decisions for affected individuals and their families.

SKU: TEST-2651 Category:

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