TPI1 Gene Triosephosphate Isomerase Deficiency Genetic Test
At DNA Labs UAE, we offer the TPI1 Gene Triosephosphate Isomerase Deficiency Genetic Test. This diagnostic test analyzes the TPI1 gene for mutations or variations that may cause triosephosphate isomerase deficiency.
Test Details
Triosephosphate isomerase deficiency is a rare genetic disorder that affects the enzyme triosephosphate isomerase, which is involved in energy production in cells. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, providing a comprehensive analysis of the TPI1 gene.
Components
- Test Name: TPI1 Gene Triosephosphate Isomerase Deficiency Genetic Test
- 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 the test, we recommend providing the clinical history of the patient who is going for the TPI1 Gene Triosephosphate Isomerase Deficiency NGS Genetic DNA Test. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected with Triosephosphate Isomerase Deficiency.
Test Process
The TPI1 Gene Triosephosphate Isomerase Deficiency NGS Genetic Test involves obtaining a sample of DNA, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, and the sequence is compared to a reference sequence to identify any variations or mutations in the TPI1 gene.
Test Results
The results of the test can help confirm a diagnosis of triosephosphate isomerase deficiency and provide information about the specific genetic variant causing the condition. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options for individuals with triosephosphate isomerase deficiency.
Test Name | TPI1 Gene Triosephosphate isomerase deficiency 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 TPI1 Gene Triosephosphate isomerase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Triosephosphate isomerase deficiency |
Test Details |
TPI1 gene triosephosphate isomerase deficiency NGS genetic test is a diagnostic test that analyzes the TPI1 gene for mutations or variations that may cause triosephosphate isomerase deficiency. Triosephosphate isomerase deficiency is a rare genetic disorder that affects the enzyme triosephosphate isomerase, which is involved in energy production in cells. NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that can analyze multiple genes simultaneously, providing a comprehensive analysis of the TPI1 gene. This test can identify specific mutations or variations in the TPI1 gene that are associated with triosephosphate isomerase deficiency. The test involves obtaining a sample of DNA, usually through a blood sample or cheek swab, and sequencing the TPI1 gene using NGS technology. The DNA sequence is then compared to a reference sequence to identify any variations or mutations that may be present. The results of the test can help confirm a diagnosis of triosephosphate isomerase deficiency and provide information about the specific genetic variant causing the condition. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options for individuals with triosephosphate isomerase deficiency. |