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CETP Gene Hyperalphalipoproteinemia Genetic Test Cost

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

-21%

The CETP Gene Hyperalphalipoproteinemia Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify variations in the CETP gene that are associated with hyperalphalipoproteinemia. This condition is characterized by unusually high levels of high-density lipoprotein (HDL) cholesterol in the blood, often referred to as “good” cholesterol due to its role in removing other forms of cholesterol from the bloodstream. Variations in the CETP gene can influence the efficiency of cholesterol transport and may impact an individual’s risk of developing cardiovascular diseases.

This genetic test is crucial for individuals with a family history of hyperalphalipoproteinemia or cardiovascular diseases, as it can provide valuable insights into their genetic predisposition to high HDL cholesterol levels. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic variations in the CETP gene.

The test is priced at 4400 AED, reflecting the comprehensive analysis and the specialized expertise required to interpret the genetic data accurately. By opting for this test at DNA Labs UAE, individuals can gain a deeper understanding of their genetic health, enabling them to make informed decisions about their lifestyle and healthcare management to potentially mitigate the risk of cardiovascular complications.

Home  Sample collection service available

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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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.

SKU: TEST-2423 Category:

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