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SARS2 Gene Hyperuricemia Pulmonary Hypertension Renal Failure and Alkalosis Genetic Test

4,400 د.إ

-21%

The “SARS2 Gene Hyperuricemia Pulmonary Hypertension Renal Failure and Alkalosis Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify genetic mutations associated with a complex spectrum of conditions. These conditions include hyperuricemia, which is an excess of uric acid in the blood; pulmonary hypertension, a type of high blood pressure that affects the arteries in the lungs and the right side of the heart; renal failure, which is a decrease in kidney function; and alkalosis, a condition where the body fluids have excess base (alkali). The test specifically looks for mutations in the SARS2 gene, which could indicate a predisposition to developing these health issues.

The cost of the test is 4400 AED, and it involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory. This genetic testing can be crucial for early diagnosis, allowing for timely intervention and management of these conditions. It can also provide valuable information for family planning and the assessment of risk for family members. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test represents a significant advancement in personalized medicine and genetic understanding of complex diseases.

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SARS2 Gene Hyperuricemia pulmonary hypertension renal failure and alkalosis Genetic Test

Welcome to the DNA Labs UAE blog, where we provide detailed information about our genetic testing services. In this article, we will discuss the SARS2 Gene Hyperuricemia pulmonary hypertension renal failure and alkalosis Genetic Test.

Test Name: SARS2 Gene Hyperuricemia pulmonary hypertension renal failure and alkalosis 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

Before undergoing the SARS2 Gene Hyperuricemia pulmonary hypertension renal failure and alkalosis Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis.

Test Details

The SARS2 gene hyperuricemia, pulmonary hypertension, renal failure, and alkalosis are health conditions that can be assessed through a Next-Generation Sequencing (NGS) genetic test. NGS is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. This test aims to identify genetic variations or mutations within the SARS2 gene and other relevant genes associated with these conditions.

Hyperuricemia is characterized by high levels of uric acid in the blood, leading to gout and kidney stones. Pulmonary hypertension is a type of high blood pressure affecting the lungs’ arteries and can lead to heart failure. Renal failure refers to the loss of kidney function, which can be caused by genetic abnormalities. Alkalosis is an imbalance in the body’s acid-base levels, resulting in elevated blood pH.

The NGS genetic test can provide valuable information for diagnosis, prognosis, and guide treatment decisions by identifying genetic variations or mutations associated with these conditions. It may also help identify individuals at risk of developing these conditions in the future, allowing for early intervention and preventive measures.

It is crucial to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who can provide appropriate counseling and guidance based on the test results.

For more information about the SARS2 Gene Hyperuricemia pulmonary hypertension renal failure and alkalosis Genetic Test or to schedule an appointment, please contact DNA Labs UAE.

Test Name SARS2 Gene Hyperuricemia pulmonary hypertension renal failure and alkalosis 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 SARS2 Gene Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis
Test Details

SARS2 gene hyperuricemia, pulmonary hypertension, renal failure, and alkalosis are all health conditions that can be assessed through a Next-Generation Sequencing (NGS) genetic test.

NGS is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. It can be used to identify genetic variations, mutations, or abnormalities that may be associated with specific diseases or conditions.

In the case of SARS2 gene hyperuricemia, pulmonary hypertension, renal failure, and alkalosis, the NGS genetic test would involve sequencing the SARS2 gene and potentially other relevant genes associated with these conditions. The test aims to identify any genetic variations or mutations within these genes that may be contributing to the development or progression of these health issues.

Hyperuricemia is a condition characterized by high levels of uric acid in the blood, which can lead to the formation of urate crystals in the joints and kidneys, causing gout and kidney stones. Pulmonary hypertension is a type of high blood pressure that affects the arteries in the lungs and can lead to heart failure. Renal failure refers to the loss of kidney function, which can occur due to various factors including genetic abnormalities. Alkalosis is a condition characterized by an imbalance in the body’s acid-base levels, resulting in elevated blood pH.

By identifying genetic variations or mutations associated with these conditions, the NGS genetic test can provide valuable information for diagnosis, prognosis, and potentially guide treatment decisions. It may also help in identifying individuals who may be at risk of developing these conditions in the future, allowing for early intervention and preventive measures.

It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who can provide appropriate counseling and guidance based on the test results.

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