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SLC2A9 Gene Hypouricemia Renal Type 2 Genetic Test Cost

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

-21%

The SLC2A9 Gene Hypouricemia Renal Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the SLC2A9 gene, which are associated with Renal Hypouricemia Type 2. This condition is characterized by abnormally low levels of uric acid in the blood, due to impaired reabsorption and increased excretion of uric acid in the kidneys. Individuals with mutations in the SLC2A9 gene may experience a range of symptoms, from asymptomatic conditions to severe complications like exercise-induced acute kidney injury.

The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of specific genetic mutations in the SLC2A9 gene. The outcome of this test can provide crucial information for the diagnosis, management, and treatment of individuals with or at risk of developing Renal Hypouricemia Type 2.

DNA Labs UAE offers this genetic test at a cost of 4400 AED. The testing process is conducted with high standards of accuracy, confidentiality, and professionalism, ensuring reliable results for patients seeking insights into their genetic predisposition to hypouricemia and its related health implications.

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SLC2A9 Gene Hypouricemia renal type 2 Genetic Test

Are you experiencing abnormally low levels of uric acid in your blood? It could be a result of a condition called hypouricemia, renal type 2. At DNA Labs UAE, we offer a comprehensive genetic test to diagnose this condition and provide personalized treatment options.

Test Details

The SLC2A9 gene is responsible for encoding a protein called glucose transporter 9 (GLUT9), primarily found in the kidneys. This protein plays a crucial role in uric acid transport. Mutations in the SLC2A9 gene can lead to hypouricemia, renal type 2.

Hypouricemia is characterized by abnormally low levels of uric acid in the blood. In renal type 2 hypouricemia, the kidneys are unable to reabsorb uric acid properly, resulting in increased excretion of uric acid in the urine and low levels in the blood.

To diagnose hypouricemia, renal type 2, we utilize NGS (Next-Generation Sequencing) technology. NGS genetic testing allows us to analyze multiple genes simultaneously, providing a comprehensive evaluation of the SLC2A9 gene.

Test Components and Price

Our SLC2A9 Gene Hypouricemia renal type 2 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is collected, the report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The SLC2A9 Gene Hypouricemia renal type 2 Genetic Test falls under the category of Hepatology, Nephrology, and Endocrinology Disorders. It is recommended to consult with a General Physician for this test.

Test Department and Pre Test Information

Our Genetics department is responsible for conducting the SLC2A9 Gene Hypouricemia renal type 2 Genetic Test. Before the test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic DNA Test gene SLC2A9.

Personalized Treatment and Management

By identifying specific mutations in the SLC2A9 gene through NGS genetic testing, we can accurately diagnose hypouricemia, renal type 2. This information is crucial for developing personalized treatment plans and managing the condition effectively.

Furthermore, the test results can be utilized for genetic counseling and identifying family members who may be at risk of developing hypouricemia, renal type 2.

Don’t wait any longer to address your abnormally low levels of uric acid. Contact DNA Labs UAE today to schedule your SLC2A9 Gene Hypouricemia renal type 2 Genetic Test!

Test Name SLC2A9 Gene Hypouricemia renal type 2 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic DNA Test gene SLC2A9
Test Details

The SLC2A9 gene is responsible for encoding a protein called glucose transporter 9 (GLUT9), which is primarily expressed in the kidneys and plays a role in uric acid transport. Mutations in the SLC2A9 gene can lead to a condition called hypouricemia, renal type 2.

Hypouricemia is a condition characterized by abnormally low levels of uric acid in the blood. In renal type 2 hypouricemia, the kidneys are unable to reabsorb uric acid properly, leading to increased excretion of uric acid in the urine and low levels in the blood.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the context of hypouricemia, NGS genetic testing can be used to identify mutations in the SLC2A9 gene that may be responsible for the condition.

By identifying specific mutations in the SLC2A9 gene, NGS genetic testing can help diagnose hypouricemia, renal type 2 and provide valuable information for personalized treatment and management of the condition. It can also be used for genetic counseling and to identify family members who may be at risk of developing the condition.

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