CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test sale cost 4400 AED
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CFHR2 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 CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the CFHR2 gene that are associated with an increased risk of developing Hemolytic Uremic Syndrome (HUS). HUS is a rare but serious condition that primarily affects kidney function and can lead to acute kidney failure. It is characterized by the triad of hemolytic anemia, thrombocytopenia, and acute renal impairment.

The test is crucial for individuals with a family history of HUS or those exhibiting symptoms of the syndrome, as it can provide valuable information for early diagnosis and management of the condition. The testing process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the CFHR2 gene.

At DNA Labs UAE, the cost of the CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to accurately identify any mutations in the CFHR2 gene. Given the complexity and the specialized nature of this genetic test, the price reflects the meticulous attention to detail and the advanced technology employed to ensure accurate results.

For patients and families affected by HUS, the CFHR2 genetic test is an invaluable tool in the management and understanding of their condition, offering insights that can guide treatment decisions and potentially improve outcomes.

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CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering comprehensive genetic testing services. In this blog, we will discuss the CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test, including its components, cost, symptoms, diagnosis, and more.

Test Name: CFHR2 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:

Prior to undergoing the CFHR2 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 CFHR2 Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test gene CFHR2.

Test Details:

The CFHR2 gene plays a crucial role in regulating the complement system, which is responsible for defending against infections. Mutations in the CFHR2 gene have been associated with an increased risk of developing hemolytic uremic syndrome (HUS), a rare condition characterized by the destruction of red blood cells, kidney damage, and low platelet count.

NGS (Next-Generation Sequencing) genetic testing is a powerful method used to analyze multiple genes simultaneously and identify any mutations or variations that may be present. In the case of hemolytic uremic syndrome, NGS genetic testing can detect mutations in the CFHR2 gene, aiding in the diagnosis of the condition.

By identifying these mutations, healthcare professionals can provide a more accurate diagnosis, assess the risk of complications, and determine the most appropriate treatment and management options for individuals with HUS. Furthermore, genetic testing can also identify other family members who may be at risk of developing the condition, enabling early intervention and preventive measures.

At DNA Labs UAE, we are committed to providing high-quality genetic testing services. Our CFHR2 Gene Hemolytic Uremic Syndrome Genetic Test offers valuable insights into the risk and management of this rare condition. To learn more or schedule an appointment, please contact our team.

Test Name CFHR2 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 CFHR2 Gene Hemolytic uremic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFHR2 Gene Hemolytic uremic syndrome NGS Genetic DNA Test gene CFHR2
Test Details

The CFHR2 gene is involved in the regulation of the complement system, which is a part of the immune system that helps to defend against infections. Mutations in the CFHR2 gene have been associated with an increased risk of developing hemolytic uremic syndrome (HUS), a rare condition characterized by the destruction of red blood cells, kidney damage, and low platelet count.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify any mutations or variations that may be present. In the case of hemolytic uremic syndrome, NGS genetic testing can be used to detect mutations in the CFHR2 gene that may be contributing to the development of the condition.

By identifying these mutations, healthcare professionals can provide a more accurate diagnosis, assess the risk of complications, and determine the most appropriate treatment and management options for individuals with HUS. Additionally, genetic testing can also help identify other family members who may be at risk of developing the condition, allowing for early intervention and preventive measures.

SKU: TEST-3641 Category:

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