IDUA Gene Hurler-Scheie Syndrome Genetic Test
Test Name: IDUA Gene Hurler-Scheie Syndrome Genetic Test
Components: IDUA gene analysis for mutations associated with Hurler-Scheie syndrome
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: Next-Generation Sequencing (NGS) Technology
Test Type: Metabolic Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for IDUA Gene Hurler-Scheie Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hurler-Scheie syndrome.
Test Details: IDUA Gene Hurler-Scheie Syndrome NGS Genetic Test is a genetic test that analyzes the IDUA gene for mutations associated with Hurler-Scheie syndrome. Hurler-Scheie syndrome is a rare genetic disorder characterized by the deficiency of the enzyme alpha-L-iduronidase, which leads to the accumulation of certain substances in the body. This test uses Next-Generation Sequencing (NGS) technology to identify variations in the IDUA gene that may be responsible for the syndrome. The results of this test can help in the diagnosis and management of Hurler-Scheie syndrome.
Test Name | IDUA Gene Hurler-Scheie syndrome 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 IDUA Gene Hurler-Scheie syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hurler-Scheie syndrome |
Test Details |
IDUA Gene Hurler-Scheie syndrome NGS Genetic Test is a genetic test that analyzes the IDUA gene for mutations associated with Hurler-Scheie syndrome. Hurler-Scheie syndrome is a rare genetic disorder characterized by the deficiency of the enzyme alpha-L-iduronidase, which leads to the accumulation of certain substances in the body. This test uses Next-Generation Sequencing (NGS) technology to identify variations in the IDUA gene that may be responsible for the syndrome. The results of this test can help in the diagnosis and management of Hurler-Scheie syndrome. |