CETP Gene Hyperalphalipoproteinemia Genetic Test
Cost: 4400.0 AED
Test Components:
- 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 CETP Gene Hyperalphalipoproteinemia NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperalphalipoproteinemia
Test Details:
CETP gene hyperalphalipoproteinemia is a condition characterized by high levels of high-density lipoprotein (HDL) cholesterol in the blood. The CETP gene provides instructions for making a protein called cholesteryl ester transfer protein (CETP), which plays a role in lipid metabolism.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA sequence. In the context of CETP gene hyperalphalipoproteinemia, NGS genetic testing can be used to identify specific variations or mutations in the CETP gene that may be associated with the condition. By analyzing the DNA sequence, NGS can help determine if an individual carries any genetic variants that may increase their risk of developing hyperalphalipoproteinemia. This information can be used for diagnostic purposes, genetic counseling, and potentially to guide treatment decisions.
It’s important to note that NGS genetic testing is just one tool in the broader context of genetic testing and should be interpreted by healthcare professionals who specialize in genetics. Additionally, the results of genetic testing should be considered in conjunction with other clinical information to make accurate and informed decisions regarding patient care.
Test Name | CETP Gene Hyperalphalipoproteinemia 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 CETP Gene Hyperalphalipoproteinemia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperalphalipoproteinemia |
Test Details |
CETP gene hyperalphalipoproteinemia is a condition characterized by high levels of high-density lipoprotein (HDL) cholesterol in the blood. The CETP gene provides instructions for making a protein called cholesteryl ester transfer protein (CETP), which plays a role in lipid metabolism. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze an individual’s DNA sequence. In the context of CETP gene hyperalphalipoproteinemia, NGS genetic testing can be used to identify specific variations or mutations in the CETP gene that may be associated with the condition. By analyzing the DNA sequence, NGS can help determine if an individual carries any genetic variants that may increase their risk of developing hyperalphalipoproteinemia. This information can be used for diagnostic purposes, genetic counseling, and potentially to guide treatment decisions. It’s important to note that NGS genetic testing is just one tool in the broader context of genetic testing and should be interpreted by healthcare professionals who specialize in genetics. Additionally, the results of genetic testing should be considered in conjunction with other clinical information to make accurate and informed decisions regarding patient care. |