NPHS1 Gene Nephrosis Finnish Type Genetic Test sale cost 4400 AED
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NPHS1 Gene Nephrosis Finnish Type Genetic Test

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

-21%

The NPHS1 gene nephrosis Finnish type genetic test is a specialized diagnostic examination designed to identify mutations in the NPHS1 gene, which are known to cause congenital nephrotic syndrome of the Finnish type (CNF). This condition is a rare genetic disorder primarily affecting the kidneys and characterized by significant protein loss in the urine, leading to swelling and a range of other health issues. The test is crucial for early detection and management of the condition, particularly in populations where the mutation is prevalent or in families with a history of the disease.

Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, and analyzing it for specific genetic alterations in the NPHS1 gene. The outcome of this test can provide essential information for the diagnosis, treatment planning, and genetic counseling of affected individuals and their families.

The cost of the NPHS1 gene nephrosis Finnish type genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify the genetic mutations associated with the condition. For families and individuals considering this test, it’s an investment in obtaining a crucial understanding of their genetic health, potentially leading to early intervention and better management of congenital nephrotic syndrome of the Finnish type.

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NPHS1 Gene Nephrosis Finnish type Genetic Test

Are you concerned about Nephrosis, Finnish type? DNA Labs UAE offers the NPHS1 Gene Nephrosis Finnish type Genetic Test at a cost of AED 4400.0. This test can help diagnose and provide valuable information for genetic counseling. Read on to learn more about this test.

Test Name: NPHS1 Gene Nephrosis Finnish type 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

Before undergoing the NPHS1 Gene Nephrosis Finnish type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with NPHS1 Gene Nephrosis, Finnish type NGS Genetic DNA Test gene NPHS1.

Test Details

The NPHS1 gene is associated with a genetic disorder called Nephrosis, Finnish type. This disorder is characterized by proteinuria (excessive protein in the urine) and nephrotic syndrome, which includes symptoms such as swelling, high cholesterol levels, and low protein levels in the blood.

NGS (Next-Generation Sequencing) genetic testing is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of the NPHS1 gene nephrosis, Finnish type, the NGS genetic test involves sequencing the NPHS1 gene to identify any genetic variations or mutations.

This test can help confirm a diagnosis of Nephrosis, Finnish type and provide information about the specific genetic variant causing the condition. It can also determine the inheritance pattern of the condition and provide information about the risk of passing it on to future generations.

NGS genetic testing for NPHS1 gene nephrosis, Finnish type is valuable for diagnosis, prognosis, and genetic counseling. It can guide treatment decisions and provide important information for affected individuals and their families.

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

The NPHS1 gene is associated with a genetic disorder called Nephrosis, Finnish type. This disorder is characterized by proteinuria (excessive protein in the urine) and nephrotic syndrome, which is a group of symptoms including swelling, high cholesterol levels, and low protein levels in the blood.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technologies to rapidly sequence DNA samples and identify genetic variations.

The NGS genetic test for NPHS1 gene nephrosis, Finnish type involves sequencing the NPHS1 gene to identify any genetic variations or mutations that may be present. This test can help confirm a diagnosis of Nephrosis, Finnish type and provide information about the specific genetic variant causing the condition.

By identifying the specific genetic variant, NGS genetic testing can also help determine the inheritance pattern of the condition and provide information about the risk of passing the condition on to future generations.

Overall, NGS genetic testing for NPHS1 gene nephrosis, Finnish type can provide valuable information for diagnosis, prognosis, and genetic counseling. It can help guide treatment decisions and provide important information for affected individuals and their families.

SKU: TEST-3731 Category:

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