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CFHR5 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 CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test is a specialized diagnostic procedure designed to identify mutations in the CFHR5 gene, which are associated with a rare form of Hemolytic Uremic Syndrome (HUS). HUS is a serious condition characterized by the triad of hemolytic anemia, acute kidney failure, and low platelet count, often triggered by an infection. However, the variant linked to the CFHR5 gene is typically atypical, meaning it does not follow the common infection-related pathway and has a genetic underpinning.

This test is particularly valuable for individuals who have a family history of HUS or present symptoms suggestive of the condition, as it can provide definitive genetic evidence of the CFHR5 mutation. Early detection through genetic testing allows for timely intervention and management of the disease, potentially preventing severe renal damage and other complications.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test is 4400 AED. Given the complexity and the specialized nature of this genetic test, the price reflects the intricate processes involved in isolating, analyzing, and interpreting the genetic data to provide a clear diagnosis. This test represents a critical step forward in the personalized care and management of patients at risk of or suffering from this rare genetic form of HUS.

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CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test

At DNA Labs UAE, we offer the CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test. This test helps in diagnosing hemolytic uremic syndrome (HUS), a rare condition characterized by the breakdown of red blood cells, kidney damage, and low platelet count.

Test Components

The CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test includes:

  • NGS Technology

Price

The cost of the CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test is AED 4400.0.

Sample Condition

The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The test report will be delivered within 3 to 4 weeks.

Method

The CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test is performed using NGS (Next-Generation Sequencing) technology.

Test Type

This test is categorized under Hepatology, Nephrology, and Endocrinology Disorders.

Referring Doctor

The CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test can be requested by a General Physician.

Test Department

This test is conducted in the Genetics department.

Pre Test Information

Prior to taking the CFHR5 Gene Hemolytic Uremic Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by CFHR5 Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test gene CFHR5.

Test Details

The CFHR5 gene is associated with hemolytic uremic syndrome (HUS). NGS genetic testing allows for the analysis of an individual’s DNA sequence. In the context of HUS, this test can identify mutations or variations in the CFHR5 gene that may contribute to the development of the condition. This information is valuable for diagnosing HUS, determining the risk of developing the condition in family members, and guiding treatment decisions.

Test Name CFHR5 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 CFHR5 Gene Hemolytic uremic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFHR5 Gene Hemolytic uremic syndrome NGS Genetic DNA Test gene CFHR5
Test Details

The CFHR5 gene is associated with hemolytic uremic syndrome (HUS), a rare condition characterized by the breakdown of red blood cells, kidney damage, and low platelet count. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. In the context of HUS, NGS genetic testing can identify mutations or variations in the CFHR5 gene that may contribute to the development of the condition. This information can be useful in diagnosing HUS, determining the risk of developing the condition in family members, and guiding treatment decisions.

SKU: TEST-3644 Category:

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