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NPHP3 Gene Nephronophthisis Type 3 Genetic Test Cost

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

-21%

The NPHP3 gene nephronophthisis type 3 genetic test is a specialized diagnostic procedure designed to identify mutations in the NPHP3 gene, which are implicated in causing nephronophthisis type 3, a rare genetic disorder. Nephronophthisis is a form of kidney disease that primarily affects children and young adults, leading to chronic kidney failure. The disease is characterized by inflammation and scarring (fibrosis) in the kidneys.

This genetic test is crucial for the accurate diagnosis of nephronophthisis type 3, enabling healthcare providers to tailor treatment plans effectively and offer genetic counseling to families. The test involves analyzing the patient’s DNA to look for specific mutations in the NPHP3 gene that are known to cause the disorder.

Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test ensures high accuracy and reliability. The cost of the NPHP3 gene nephronophthisis type 3 genetic test is 4400 AED, reflecting the comprehensive analysis and expertise required to conduct this specialized diagnostic procedure. By opting for this test, patients and their families can gain valuable insights into the genetic basis of nephronophthisis type 3, facilitating better management of the condition and informed decision-making regarding family planning.

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NPHP3 Gene Nephronophthisis type 3 Genetic Test

Welcome to DNA Labs UAE, where we offer the NPHP3 Gene Nephronophthisis type 3 Genetic Test. This test is designed to detect and analyze mutations or variants in the NPHP3 gene, which is associated with a genetic disorder called nephronophthisis type 3 (NPHP3).

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

Prior to undergoing the NPHP3 Gene Nephronophthisis type 3 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 with the NPHP3 gene. This information will help in understanding the inheritance pattern and assessing the risk of developing nephronophthisis type 3.

Test Details

NPHP3 is a rare autosomal recessive disorder that primarily affects the kidneys and can lead to chronic kidney disease and end-stage renal disease. Our NGS genetic testing utilizes Next-Generation Sequencing technology, which allows for the simultaneous analysis of multiple genes, including the NPHP3 gene. This comprehensive analysis enables the identification of mutations or variants in the NPHP3 gene, aiding in the confirmation of a diagnosis and understanding the underlying cause of the disease.

NGS technology is capable of sequencing a large number of DNA fragments in parallel, providing a detailed analysis of the entire gene or multiple genes at once. The results of the NPHP3 Gene Nephronophthisis type 3 Genetic Test can provide valuable information for treatment and management options, as well as offering guidance for the patient and their family.

Please note that NGS genetic testing for NPHP3 is typically performed in a clinical setting by healthcare professionals with expertise in genetics. It is crucial to interpret and discuss the results with a healthcare provider or genetic counselor to fully comprehend the implications and potential impact on the individual and their family.

Test Name NPHP3 Gene Nephronophthisis 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 NPHP3 Gene Nephronophthisis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NPHP3 Gene Nephronophthisis type 3 NGS Genetic DNA Test gene NPHP3
Test Details

The NPHP3 gene is associated with a genetic disorder called nephronophthisis type 3 (NPHP3). NPHP3 is a rare autosomal recessive disorder that affects the kidneys and can lead to chronic kidney disease and end-stage renal disease.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the NPHP3 gene. NGS technology enables the sequencing of a large number of DNA fragments in parallel, providing a comprehensive analysis of the entire gene or multiple genes at once.

NGS genetic testing for NPHP3 can be used to identify mutations or variants in the NPHP3 gene that may be causing or contributing to the development of nephronophthisis type 3. This information can help in confirming a diagnosis, understanding the underlying cause of the disease, and providing guidance for treatment and management options.

It is important to note that NGS genetic testing for NPHP3 is typically performed in a clinical setting by healthcare professionals with expertise in genetics. The results of the test should be interpreted and discussed with a healthcare provider or genetic counselor to fully understand the implications and potential impact on the individual and their family.