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CFHR3 Gene Hemolytic Uremic Syndrome Genetic Test Cost

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

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The CFHR3 Gene Hemolytic Uremic Syndrome Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the CFHR3 gene, which can be linked to atypical hemolytic uremic syndrome (aHUS), a rare, life-threatening condition. aHUS is characterized by the triad of hemolytic anemia, thrombocytopenia, and acute renal failure. It is distinguished from typical HUS by its lack of association with infections caused by certain strains of E. coli. Instead, aHUS results from uncontrolled activation of the complement system, a part of the body’s immune response, which can be triggered by genetic factors such as mutations in the CFHR3 gene.

The test, which costs 4400 AED, is available at DNA Labs UAE, a leading facility in genetic and molecular diagnostics. By analyzing a patient’s DNA sample, usually obtained from blood, this test can identify specific genetic variations in the CFHR3 gene that are known to increase the risk of developing aHUS. Early identification of these mutations can be crucial for affected individuals and their families, as it allows for timely intervention and management of the condition. It also aids in the understanding of the genetic basis of the disease, facilitating personalized treatment approaches that can significantly improve patient outcomes.

DNA Labs UAE employs state-of-the-art technology and follows rigorous protocols to ensure the accuracy and reliability of the test results. The facility is staffed by experienced professionals who are dedicated to providing comprehensive support and guidance throughout the testing process.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CFHR3 Gene Hemolytic Uremic Syndrome Genetic Test

At DNA Labs UAE, we offer the CFHR3 Gene Hemolytic Uremic Syndrome Genetic Test at a cost of AED 4400.0. This test is used to diagnose and identify genetic variations or mutations associated with Hemolytic Uremic Syndrome (HUS).

Test Components

The CFHR3 Gene Hemolytic Uremic Syndrome Genetic Test includes:

  • 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 the CFHR3 Gene Hemolytic Uremic Syndrome 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 by the CFHR3 Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test gene CFHR3.

Test Details

The CFHR3 gene is associated with Hemolytic Uremic Syndrome (HUS), a rare disorder characterized by the destruction of red blood cells, low platelet count, and kidney failure. HUS is usually caused by an infection, such as certain strains of E. coli bacteria.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously in order to identify genetic variations or mutations that may be associated with a particular condition. In the case of Hemolytic Uremic Syndrome, NGS genetic testing can help identify mutations or variations in the CFHR3 gene that may contribute to the development of the condition.

By analyzing the CFHR3 gene, NGS genetic testing can aid in the diagnosis of Hemolytic Uremic Syndrome and provide information about the genetic factors that may be contributing to the condition. This information can be valuable in determining appropriate treatment and management strategies for individuals with HUS.

Test Name CFHR3 Gene Hemolytic uremic 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 CFHR3 Gene Hemolytic uremic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFHR3 Gene Hemolytic uremic syndrome NGS Genetic DNA Test gene CFHR3
Test Details

The CFHR3 gene is associated with a condition called Hemolytic Uremic Syndrome (HUS). HUS is a rare disorder characterized by the destruction of red blood cells, low platelet count, and kidney failure. It is usually caused by an infection, such as certain strains of E. coli bacteria.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of Hemolytic Uremic Syndrome, NGS genetic testing can be used to identify mutations or variations in the CFHR3 gene that may contribute to the development of the condition.

By analyzing the CFHR3 gene, NGS genetic testing can help in the diagnosis of Hemolytic Uremic Syndrome and provide information about the genetic factors that may be contributing to the condition. This information can be useful in determining the appropriate treatment and management strategies for individuals with HUS.

SKU: TEST-3642 Category:

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