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NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test Cost

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

-21%

The NPHS1 gene plays a crucial role in kidney function, and mutations in this gene are associated with Nephrotic Syndrome Type 2, a genetic disorder characterized by significant proteinuria, hypoalbuminemia, and edema. This condition can lead to severe kidney damage and failure if not diagnosed and managed appropriately. The genetic test for NPHS1 gene mutations is a crucial tool in the diagnosis and management of Nephrotic Syndrome Type 2. It helps in identifying the genetic cause of the condition, enabling personalized treatment plans and informing family planning decisions.

DNA Labs UAE offers a comprehensive genetic test for the NPHS1 gene to identify mutations associated with Nephrotic Syndrome Type 2. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately detect and interpret genetic variations. Conducted in a state-of-the-art laboratory by experienced geneticists, the test involves analyzing the patient’s DNA sample, usually obtained through a simple blood draw. Results from this test can provide valuable insights into the genetic basis of the condition, guiding treatment options and helping to predict the risk of passing the condition to future generations.

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NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test

Test Name: NPHS1 Gene Nephrotic Syndrome Type 2 Genetic Test

Components: NGS Technology

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 NPHS1 Gene Nephrotic Syndrome Type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NPHS1 Gene Nephrotic Syndrome Type 2 NGS Genetic DNA Test gene NPHS1

Test Details

The NPHS1 gene is associated with a genetic disorder called Nephrotic Syndrome Type 2. Nephrotic syndrome is a kidney disorder characterized by the presence of excessive protein in the urine, low levels of protein in the blood, high cholesterol levels, and swelling in various parts of the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously. In the context of Nephrotic Syndrome Type 2, NGS genetic testing can be used to identify mutations or variations in the NPHS1 gene that may be responsible for the development of the disorder.

By analyzing the entire coding region of the NPHS1 gene, NGS genetic testing can provide comprehensive and accurate results, helping to confirm a diagnosis of Nephrotic Syndrome Type 2 and guide appropriate treatment and management options.

Test Name NPHS1 Gene Nephrotic syndrome 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 NPHS1 Gene Nephrotic syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NPHS1 Gene Nephrotic syndrome type 2 NGS Genetic DNA Test gene NPHS1
Test Details

The NPHS1 gene is associated with a genetic disorder called Nephrotic syndrome type 2. Nephrotic syndrome is a kidney disorder characterized by the presence of excessive protein in the urine, low levels of protein in the blood, high cholesterol levels, and swelling in various parts of the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that analyzes multiple genes simultaneously. In the context of Nephrotic syndrome type 2, NGS genetic testing can be used to identify mutations or variations in the NPHS1 gene that may be responsible for the development of the disorder.

By analyzing the entire coding region of the NPHS1 gene, NGS genetic testing can provide comprehensive and accurate results, helping to confirm a diagnosis of Nephrotic syndrome type 2 and guide appropriate treatment and management options.