APOA2 Gene Apolipoprotein A-II Deficiency Genetic Test
At DNA Labs UAE, we offer the APOA2 Gene Apolipoprotein A-II Deficiency Genetic Test to help diagnose individuals with this rare genetic condition. This test is essential for those experiencing low levels of apolipoprotein A-II in their blood, which can lead to altered lipid metabolism and an increased risk of cardiovascular disease.
Test Details
The APOA2 gene encodes the apolipoprotein A-II protein, a component of high-density lipoprotein (HDL) cholesterol. HDL cholesterol, also known as “good” cholesterol, plays a crucial role in removing excess cholesterol from the bloodstream and transporting it to the liver for excretion.
The APOA2 Gene Apolipoprotein A-II Deficiency Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of an individual’s genes. This technique can identify variations or mutations in specific genes, including the APOA2 gene, associated with certain genetic conditions or traits.
Test Components and Price
- Test Name: APOA2 Gene Apolipoprotein A-II Deficiency Genetic Test
- Components: Blood or Extracted DNA or One drop Blood on FTA Card
- 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 APOA2 Gene Apolipoprotein A-II Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Apolipoprotein A-II deficiency.
Diagnosis and Medical Management
If you suspect you have Apolipoprotein A-II deficiency, it is crucial to undergo genetic testing performed and interpreted by qualified healthcare professionals. This ensures accurate and personalized information about your genetic makeup and associated risks.
Once diagnosed, appropriate medical management and genetic counseling can be provided. Genetic counseling helps individuals understand the implications of their genetic test results and make informed decisions about their health and family planning.
Conclusion
The APOA2 Gene Apolipoprotein A-II Deficiency Genetic Test offered at DNA Labs UAE is a vital tool for diagnosing individuals with this rare genetic condition. With accurate genetic testing and personalized medical management, individuals can better understand their risks and make informed decisions about their health and well-being.
| Test Name | APOA2 Gene Apolipoprotein A-II 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 APOA2 Gene Apolipoprotein A-II deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Apolipoprotein A-II deficiency |
| Test Details |
The APOA2 gene encodes the apolipoprotein A-II protein, which is a component of high-density lipoprotein (HDL) cholesterol. HDL cholesterol is often referred to as “good” cholesterol because it helps remove excess cholesterol from the bloodstream and transport it to the liver for excretion. Apolipoprotein A-II deficiency is a rare genetic condition that is characterized by low levels of apolipoprotein A-II in the blood. This condition is associated with altered lipid metabolism and an increased risk of cardiovascular disease. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It can identify variations or mutations in specific genes, including the APOA2 gene, that may be associated with certain genetic conditions or traits. In the case of APOA2 gene testing, NGS can be used to detect variations or mutations in the gene that may be responsible for apolipoprotein A-II deficiency. This can help diagnose individuals with the condition and provide them with appropriate medical management and genetic counseling. It’s important to note that genetic testing should be performed and interpreted by qualified healthcare professionals who can provide accurate and personalized information about an individual’s genetic makeup and associated risks. |
