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PLCE1 Gene Nephrotic Syndrome Type 3 Genetic Test Cost

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

-21%

The PLCE1 Gene Nephrotic Syndrome Type 3 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the PLCE1 gene, which are associated with Nephrotic Syndrome Type 3. This condition, also known as familial steroid-resistant nephrotic syndrome, is characterized by significant proteinuria, hypoalbuminemia, hyperlipidemia, and edema. It is a rare genetic disorder that affects the kidneys’ filtering system, leading to a loss of protein in the urine and reduced ability to regulate water and salt levels in the body.

The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost of the test is 4400 AED. This investment in testing is crucial for families with a history of the condition or for individuals showing symptoms of nephrotic syndrome, as early detection can significantly influence the management and treatment options for affected individuals. The results from this genetic test can provide valuable information for healthcare providers to develop a personalized treatment plan, potentially involving medication, dietary adjustments, and in some cases, consideration of genetic counseling for the family.

Understanding the genetic basis of Nephrotic Syndrome Type 3 through the PLCE1 gene test is an essential step in advancing patient care and improving outcomes for those affected by this challenging condition.

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PLCE1 Gene Nephrotic Syndrome Type 3 Genetic Test

At DNA Labs UAE, we offer the PLCE1 Gene Nephrotic Syndrome Type 3 Genetic Test to help diagnose and determine the best course of treatment for individuals with nephrotic syndrome. This genetic test analyzes the PLCE1 gene, which is associated with nephrotic syndrome type 3.

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

Before undergoing the PLCE1 Gene Nephrotic Syndrome Type 3 Genetic Test, it is important 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 PLCE1 gene.

Test Details

Nephrotic syndrome is a kidney disorder characterized by protein in the urine, low levels of protein in the blood, high cholesterol levels, and swelling in various parts of the body. The PLCE1 gene is specifically associated with nephrotic syndrome type 3. Our NGS genetic testing uses advanced sequencing technologies to analyze multiple genes simultaneously.

For nephrotic syndrome type 3, the NGS genetic test can identify mutations or variations in the PLCE1 gene that may contribute to the development of the condition. This test aids in diagnosing nephrotic syndrome type 3 and determining the most effective treatment plan. It can also be used for genetic counseling and assessing the risk of passing on the condition to future generations.

It is crucial to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor. They can provide appropriate guidance and support based on the test results.

Test Name PLCE1 Gene Nephrotic syndrome type 3 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 PLCE1 Gene Nephrotic syndrome type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PLCE1 Gene Nephrotic syndrome type 3 NGS Genetic DNA Test gene PLCE1
Test Details

The PLCE1 gene is associated with a form of nephrotic syndrome called nephrotic syndrome type 3. Nephrotic syndrome is a kidney disorder characterized by the presence of protein in the urine, low levels of protein in the blood, high cholesterol levels, and swelling (edema) in various parts of the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of nephrotic syndrome type 3, NGS genetic testing can be used to identify mutations or variations in the PLCE1 gene that may be responsible for the development of the condition.

By identifying these genetic variations, NGS genetic testing can help in diagnosing nephrotic syndrome type 3 and determining the best course of treatment for affected individuals. It can also be used for genetic counseling and to assess the risk of passing on the condition to future generations.

It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the results.