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AGTR1 Gene Renal tubular dysgenesis Genetic Test

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

-21%

The AGTR1 gene plays a crucial role in the regulation of blood pressure and fluid balance in the body, and mutations in this gene can lead to a rare, severe condition known as renal tubular dysgenesis (RTD). RTD is characterized by poor development of the kidney’s tubules, leading to life-threatening complications shortly after birth, including an inability to produce urine (anuria), low blood pressure, and respiratory distress.

To diagnose this condition, a genetic test targeting the AGTR1 gene can be performed. This test is particularly vital for families with a history of RTD or for newborns showing symptoms consistent with the disorder. By analyzing the DNA sequence of the AGTR1 gene, the test can identify mutations that are known to cause RTD, providing crucial information for diagnosis, management, and genetic counseling.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for AGTR1 gene mutations. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures that patients and their families have access to cutting-edge genetic testing technology, expert analysis, and comprehensive support throughout the testing process. The results from this test can help guide clinical decisions, including potential treatments and interventions to manage the symptoms associated with RTD, and offer families vital information about the genetic risk of RTD in future pregnancies.

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AGTR1 Gene Renal Tubular Dysgenesis Genetic Test

Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. Today, we will be discussing the AGTR1 Gene Renal Tubular Dysgenesis Genetic Test, its components, cost, symptoms, diagnosis, and other important details.

Test Details

The AGTR1 gene is associated with a rare genetic disorder called renal tubular dysgenesis (RTD). This condition affects the development of the kidneys, specifically the renal tubules. The renal tubules play a crucial role in filtering waste products from the blood and reabsorbing essential substances back into the body.

Mutations in the AGTR1 gene can disrupt the normal development and function of the renal tubules, leading to severe impairment of kidney function. This can result in various symptoms, including low amniotic fluid levels during pregnancy, abnormal kidney development, and early-onset kidney failure in newborns.

Components and Price

The AGTR1 Gene Renal Tubular Dysgenesis Genetic Test costs AED 4400.0. The test requires a blood sample for analysis.

Method

The AGTR1 Gene Renal Tubular Dysgenesis Genetic Test is conducted using NGS (Next-Generation Sequencing) technology. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive genetic profile.

Test Type and Doctor

The AGTR1 Gene Renal Tubular Dysgenesis Genetic Test falls under the field of Hepatology, Nephrology, and Endocrinology Disorders. It is typically recommended to consult with a General Physician before undergoing this test.

Test Department

The AGTR1 Gene Renal Tubular Dysgenesis Genetic Test is conducted in our Genetics department.

Pre-Test Information

Before undergoing the AGTR1 Gene Renal Tubular Dysgenesis Genetic Test, it is essential to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the AGTR1 gene.

Report Delivery

The report for the AGTR1 Gene Renal Tubular Dysgenesis Genetic Test is typically delivered within 3 to 4 weeks.

Importance of Genetic Testing

Genetic testing for RTD is recommended for individuals with a suspected or confirmed diagnosis of the condition. It can provide crucial information for genetic counseling and family planning. However, it is important to note that genetic testing can be complex and should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

At DNA Labs UAE, we prioritize accurate and reliable genetic testing to assist in the diagnosis and management of various genetic disorders. Contact us today to schedule your AGTR1 Gene Renal Tubular Dysgenesis Genetic Test.

Test Name AGTR1 Gene Renal tubular dysgenesis Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 AGTR1 Gene Renal tubular dysgenesis NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with AGTR1 Gene Renal tubular dysgenesis NGS Genetic DNA Test gene AGTR1
Test Details

The AGTR1 gene is associated with a condition called renal tubular dysgenesis (RTD). RTD is a rare genetic disorder that affects the development of the kidneys, specifically the renal tubules. The renal tubules are responsible for filtering waste products from the blood and reabsorbing essential substances back into the body.

Mutations in the AGTR1 gene can disrupt the normal development and function of the renal tubules, leading to severe impairment of kidney function. This can result in a variety of symptoms, including low amniotic fluid levels during pregnancy, abnormal kidney development, and early-onset kidney failure in newborns.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of renal tubular dysgenesis, NGS genetic testing can be used to identify mutations in the AGTR1 gene that may be causing the condition. This can help with the diagnosis of RTD and provide important information for genetic counseling and family planning.

It is important to note that genetic testing for RTD is typically recommended for individuals with a suspected or confirmed diagnosis of the condition. Genetic testing can be complex and should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.