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LPL Gene Hyperlipoproteinemia Type 1 Genetic Test Cost

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

-21%

The LPL Gene Hyperlipoproteinemia Type 1 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the LPL gene, which can lead to Type 1 hyperlipoproteinemia. This condition, also known as familial lipoprotein lipase deficiency, is a rare genetic disorder characterized by the inability to properly break down fats, leading to an accumulation of chylomicrons and triglycerides in the blood, and potentially resulting in pancreatitis, abdominal pain, and other complications.

The test is crucial for individuals with a family history of hyperlipoproteinemia or those who have symptoms of the disorder, as it helps in confirming the diagnosis, enabling personalized treatment plans, and informing family planning decisions. Conducted through a simple blood sample, the genetic analysis focuses on detecting specific mutations within the LPL gene that are responsible for the condition.

At DNA Labs UAE, the LPL Gene Hyperlipoproteinemia Type 1 Genetic Test is priced at 4400 AED. This cost reflects the comprehensive nature of the testing process, from the initial sample collection to the detailed genetic analysis and the provision of a conclusive report by the lab’s expert geneticists. The test is an invaluable tool for affected individuals and their families to understand their genetic health, manage the condition effectively, and make informed healthcare decisions.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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LPL Gene Hyperlipoproteinemia Type 1 Genetic Test

Test Name: LPL Gene Hyperlipoproteinemia Type 1 Genetic Test

Components: DNA Labs UAE offers the LPL Gene Hyperlipoproteinemia Type 1 Genetic Test at a price of 4400.0 AED.

Sample Condition: The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery: The test results will be delivered within 3 to 4 weeks.

Method: The LPL Gene Hyperlipoproteinemia Type 1 Genetic Test utilizes NGS (Next-Generation Sequencing) technology.

Test Type: This test is specifically designed for detecting metabolic disorders.

Doctor: The test can be ordered by a general physician.

Test Department: DNA Labs UAE’s Genetics department handles the LPL Gene Hyperlipoproteinemia Type 1 Genetic Test.

Pre Test Information: Prior to the test, a clinical history of the patient is required. Additionally, a genetic counseling session is conducted to create a pedigree chart of family members affected by Hyperlipoproteinemia Type 1.

Test Details: The LPL Gene Hyperlipoproteinemia Type 1 Genetic Test is a genetic test that analyzes the LPL gene for mutations associated with Hyperlipoproteinemia Type 1. This rare genetic disorder impairs the breakdown of certain fats, resulting in the accumulation of chylomicrons in the blood. Symptoms of this condition may include abdominal pain, pancreatitis, and eruptive xanthomas. NGS technology allows for the simultaneous analysis of multiple genes. In this test, NGS is used to sequence the LPL gene and identify any mutations or variants present. By identifying these genetic changes, healthcare professionals can provide a more accurate diagnosis, assess disease severity, and make informed treatment decisions for individuals with Hyperlipoproteinemia Type 1.

Test Name LPL Gene Hyperlipoproteinemia type 1 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 LPL Gene Hyperlipoproteinemia type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperlipoproteinemia type 1
Test Details

LPL Gene Hyperlipoproteinemia type 1 NGS Genetic Test is a genetic test that analyzes the LPL gene for mutations associated with Hyperlipoproteinemia type 1. Hyperlipoproteinemia type 1 is a rare genetic disorder characterized by the inability to break down certain fats, leading to the accumulation of chylomicrons in the blood. This condition can result in symptoms such as abdominal pain, pancreatitis, and eruptive xanthomas.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology used to analyze multiple genes simultaneously. This test uses NGS technology to sequence the LPL gene and identify any mutations or variants that may be present. By identifying these genetic changes, healthcare professionals can provide a more accurate diagnosis, assess disease severity, and guide treatment decisions for individuals with Hyperlipoproteinemia type 1.