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GSTZ1 Gene Tyrosinemia type 1B Genetic Test Cost

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

-21%

The “GSTZ1 Gene Tyrosinemia Type 1B Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the GSTZ1 gene, which are linked to Tyrosinemia type 1B, a rare genetic disorder. This condition affects the body’s ability to properly break down the amino acid tyrosine, leading to various health issues, including liver and kidney problems. The test is crucial for early detection and management of the disorder, enabling healthcare providers to tailor appropriate treatment plans for affected individuals. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the genetic variations associated with Tyrosinemia type 1B.

Description

GSTZ1 Gene Tyrosinemia type 1B Genetic Test

Cost: AED 4400.0

Test Components: GSTZ1 Gene Tyrosinemia type 1B Genetic Test

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 GSTZ1 Gene Tyrosinemia type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosinemia type 1B.

Test Details:

The GSTZ1 gene is associated with a condition called tyrosinemia type 1B. Tyrosinemia type 1 is a rare genetic disorder that affects the body’s ability to break down the amino acid tyrosine. This can lead to a buildup of toxic substances in the body, which can cause liver and kidney damage.

NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the analysis of multiple genes at once. In the case of tyrosinemia type 1B, NGS can be used to identify mutations or variations in the GSTZ1 gene that may be responsible for the condition. By analyzing the GSTZ1 gene using NGS, healthcare professionals can determine if a person has any genetic variants that are associated with tyrosinemia type 1B. This information can be used for diagnosis, genetic counseling, and potentially for treatment options.

It is important to note that genetic testing for tyrosinemia type 1B should be performed by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and interpretation of the results.

Test Name	GSTZ1 Gene Tyrosinemia type 1B 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 GSTZ1 Gene Tyrosinemia type 1B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosinemia type 1B
Test Details	The GSTZ1 gene is associated with a condition called tyrosinemia type 1B. Tyrosinemia type 1 is a rare genetic disorder that affects the body’s ability to break down the amino acid tyrosine. This can lead to a buildup of toxic substances in the body, which can cause liver and kidney damage. NGS (Next-Generation Sequencing) is a type of genetic testing that allows for the analysis of multiple genes at once. In the case of tyrosinemia type 1B, NGS can be used to identify mutations or variations in the GSTZ1 gene that may be responsible for the condition. By analyzing the GSTZ1 gene using NGS, healthcare professionals can determine if a person has any genetic variants that are associated with tyrosinemia type 1B. This information can be used for diagnosis, genetic counseling, and potentially for treatment options. It is important to note that genetic testing for tyrosinemia type 1B should be performed by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and interpretation of the results.