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LPA Gene LPA Deficiency Congenital Genetic Test Cost

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

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The LPA gene is crucial for the production of lipoprotein(a), a type of low-density lipoprotein (LDL) often referred to as “bad cholesterol.” Variations or mutations in the LPA gene can lead to either elevated levels of lipoprotein(a), increasing the risk of cardiovascular diseases, or LPA deficiency, which is less common and has varying implications on health.

LPA deficiency is a congenital condition, meaning it is present from birth and is inherited in a genetic manner. Individuals with this deficiency might have lower risks of cardiovascular diseases, but the full implications of this condition are not completely understood and can vary widely among affected individuals.

To diagnose this condition, a specific genetic test can be conducted. In the UAE, DNA Labs offers a comprehensive genetic test targeting the LPA gene to identify mutations or variations that might indicate LPA deficiency or other related conditions. The test is priced at 4400 AED. It is a crucial tool for individuals with a family history of cardiovascular diseases or those who have personal health concerns related to cholesterol and heart health. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic markers associated with the LPA gene.

Understanding one’s genetic predisposition to LPA deficiency or elevated lipoprotein(a) levels can be an important step in managing and mitigating potential health risks, allowing for personalized medical advice and interventions.

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LPA Gene LPA Deficiency Congenital Genetic Test – Cost AED 4400.0

Genetic testing plays a crucial role in identifying and understanding various genetic conditions. One such condition is LPA deficiency, which can be diagnosed through the LPA Gene LPA Deficiency Congenital Genetic Test.

Test Details

The LPA gene, also known as the Lipoprotein(a) gene, is responsible for the production of lipoprotein(a) in the body. Lipoprotein(a) is a cholesterol particle involved in the transport of fats in the blood. High levels of lipoprotein(a) have been associated with an increased risk of cardiovascular diseases, such as heart attacks and strokes.

LPA deficiency refers to a condition where there is a reduced or absent production of lipoprotein(a) in the body. This deficiency can be caused by genetic mutations in the LPA gene, which affect its ability to produce the protein. Although LPA deficiency is relatively rare, its clinical significance is still not fully understood.

The LPA Gene LPA Deficiency Congenital Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. This advanced sequencing technology allows for the detection of genetic variations, including mutations, in a person’s DNA. By identifying mutations in the LPA gene, the test can aid in the diagnosis and management of individuals with LPA deficiency.

It is important to note that the presence of a genetic mutation does not necessarily mean that a person will develop the associated health risks. Other factors, such as lifestyle choices and environmental factors, also contribute to an individual’s risk for cardiovascular diseases.

Test Components and Price

  • Test Name: LPA Gene LPA Deficiency Congenital Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: AED 4400.0
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the LPA Gene LPA Deficiency Congenital Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by LPA deficiency, congenital.

Conclusion

If you are concerned about LPA deficiency or have a family history of cardiovascular diseases, it is highly recommended to consult with a healthcare professional or a genetic counselor. They can provide you with more information and guidance regarding genetic testing options and help you understand the implications of the test results.

Test Name LPA Gene LPA deficiency congenital 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 LPA Gene LPA deficiency, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LPA deficiency, congenital
Test Details

LPA gene, also known as Lipoprotein(a) gene, is responsible for the production of a protein called lipoprotein(a) in the body. Lipoprotein(a) is a type of cholesterol particle that is involved in the transport of fats in the blood. However, high levels of lipoprotein(a) in the blood have been associated with an increased risk of cardiovascular diseases, such as heart attacks and strokes.

LPA deficiency refers to a condition where there is a reduced or absent production of lipoprotein(a) in the body. This can be caused by genetic mutations in the LPA gene, which affect its ability to produce the protein. LPA deficiency is relatively rare and its clinical significance is still not fully understood.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of genetic variations, including mutations, in a person’s DNA. NGS genetic testing can be used to identify mutations in the LPA gene that may be responsible for LPA deficiency. This can help in the diagnosis and management of individuals with this condition.

It is important to note that LPA deficiency is a complex condition, and the presence of a genetic mutation does not necessarily mean that a person will develop the associated health risks. Other factors, such as lifestyle choices and environmental factors, also play a role in determining an individual’s risk for cardiovascular diseases.

If you are concerned about LPA deficiency or have a family history of cardiovascular diseases, it is recommended to consult with a healthcare professional or a genetic counselor who can provide you with more information and guidance regarding genetic testing options.

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