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NPHS2 Gene Nephrotic Syndrome Genetic Test Cost

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

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The NPHS2 Gene Nephrotic Syndrome Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the NPHS2 gene, which are known to cause steroid-resistant nephrotic syndrome (SRNS). This condition is characterized by significant proteinuria, hypoalbuminemia, and edema, and it does not respond to standard steroid treatments, making genetic testing crucial for accurate diagnosis and management. The NPHS2 gene encodes podocin, a protein essential for the proper function of the glomeruli in the kidneys. Mutations in this gene can disrupt kidney function, leading to SRNS.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, this test offers a comprehensive analysis for individuals suspected of having SRNS, especially when there is a family history of kidney diseases or when the condition does not improve with conventional treatments. The test is priced at 4400 AED, reflecting the intricate technology and expertise required to accurately detect mutations in the NPHS2 gene.

Upon completion, the results can provide valuable insights into the genetic underpinnings of the nephrotic syndrome in the patient, guiding healthcare providers in tailoring a more effective treatment plan. This may include adjustments in medication, consideration of genetic counseling for the family, and in some cases, preparation for kidney transplantation. Given the complexity and the potential severity of SRNS, the NPHS2 Gene Nephrotic Syndrome Genetic Test represents a critical step towards personalized medicine in nephrology.

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NPHS2 Gene Nephrotic Syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the NPHS2 Gene Nephrotic Syndrome Genetic Test. This test is designed to analyze the NPHS2 gene and identify any genetic variations or mutations that may be associated with nephrotic syndrome.

Test Details

The NPHS2 gene encodes for a protein called podocin, which is a crucial component of the filtration barrier in the kidneys. Mutations in this gene can lead to nephrotic syndrome, a kidney disorder characterized by excessive protein loss in the urine, low protein levels in the blood, high cholesterol levels, and swelling in various parts of the body.

Our NPHS2 Gene Nephrotic Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously, including the NPHS2 gene. This advanced genetic testing method involves sequencing the DNA of an individual to identify any genetic variations or mutations that may be present.

Test Components and Price

The NPHS2 Gene Nephrotic Syndrome Genetic Test is priced at 4400.0 AED. The test can be performed using a blood sample, extracted DNA, or just one drop of blood on an FTA card.

Report Delivery and Test Type

Once the sample is received, the report will be delivered within 3 to 4 weeks. The NPHS2 Gene Nephrotic Syndrome Genetic Test falls under the Hepatology, Nephrology, and Endocrinology Disorders category.

Referring Doctor and Test Department

This test can be requested by a General Physician and is conducted in our Genetics department.

Pre Test Information

Prior to undergoing the NPHS2 Gene Nephrotic Syndrome Genetic Test, it is important 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 NPHS2 Gene Nephrotic Syndrome NGS Genetic DNA Test gene NPHS2.

Benefits of the Test

The NPHS2 Gene Nephrotic Syndrome Genetic Test can help diagnose the underlying genetic cause of nephrotic syndrome, providing valuable information about the specific genetic mutation present in the NPHS2 gene. This information is essential for determining the appropriate treatment and management strategies for individuals with nephrotic syndrome. It can also aid in genetic counseling and predicting the risk of passing on the condition to future generations.

Test Name NPHS2 Gene Nephrotic syndrome 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 NPHS2 Gene Nephrotic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NPHS2 Gene Nephrotic syndrome NGS Genetic DNA Test gene NPHS2
Test Details

The NPHS2 gene is a gene that encodes for a protein called podocin. Podocin is an important component of the filtration barrier in the kidneys. Mutations in the NPHS2 gene can lead to a condition called nephrotic syndrome.

Nephrotic syndrome is a kidney disorder characterized by excessive protein loss in the urine, low levels of protein in the blood, high cholesterol levels, and swelling (edema) in various parts of the body. It can be caused by a variety of genetic and non-genetic factors.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can be used to analyze multiple genes simultaneously, including the NPHS2 gene. It involves sequencing the DNA of an individual to identify any genetic variations or mutations that may be associated with a particular condition, such as nephrotic syndrome.

NGS genetic testing can help in diagnosing the underlying genetic cause of nephrotic syndrome, providing information about the specific genetic mutation present in the NPHS2 gene. This information can be useful for determining the appropriate treatment and management strategies for individuals with nephrotic syndrome. It can also help in providing genetic counseling and predicting the risk of passing on the condition to future generations.

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