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CFHR4 Gene Hemolytic Uremic Syndrome Genetic Test Cost

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

-21%

The CFHR4 Gene Hemolytic Uremic Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the CFHR4 gene that are associated with Hemolytic Uremic Syndrome (HUS). HUS is a rare but severe condition characterized by the destruction of red blood cells, failure of the kidneys, and low platelet count. This condition can lead to serious complications, including kidney failure and potentially life-threatening situations if not diagnosed and treated promptly.

The CFHR4 gene plays a crucial role in the regulation of the complement system, which is part of the body’s immune response. Mutations in this gene can disrupt the normal functioning of the complement system, leading to the development of HUS. By identifying these genetic mutations, the test provides critical information that can guide healthcare professionals in making accurate diagnoses, prognostic assessments, and decisions regarding the most appropriate treatment strategies for affected individuals.

The test is conducted at DNA Labs UAE, a state-of-the-art facility known for its advanced genetic testing services. The cost of the CFHR4 Gene Hemolytic Uremic Syndrome Genetic Test is 4400 AED. This investment includes the collection of a DNA sample, usually through a blood draw, followed by detailed genetic analysis to detect any mutations in the CFHR4 gene.

For patients suspected of having HUS, or for those with a family history of the condition, this test can be an invaluable tool in managing and understanding their health, potentially preventing serious outcomes by facilitating early and targeted interventions.

Description

CFHR4 Gene Hemolytic Uremic Syndrome Genetic Test

Test Name: CFHR4 Gene Hemolytic Uremic Syndrome Genetic Test

Components: CFHR4 gene analysis

Price: AED 4400.0

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 CFHR4 Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFHR4 Gene Hemolytic Uremic Syndrome NGS Genetic DNA Test gene CFHR4.

Test Details: The CFHR4 gene is one of the complement factor H-related genes. Hemolytic uremic syndrome (HUS) is a rare disorder characterized by the destruction of red blood cells, low platelet count, and kidney failure. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup. The CFHR4 gene is associated with atypical hemolytic uremic syndrome (aHUS), which is a form of HUS that is not caused by an infection. Mutations or variations in the CFHR4 gene can lead to abnormal complement regulation, which can trigger the immune system to attack and damage red blood cells, leading to HUS. NGS genetic testing for the CFHR4 gene can help identify mutations or variations in the gene that may contribute to the development of HUS. This information can be used for diagnosis, genetic counseling, and potentially guiding treatment decisions. However, it is important to note that genetic testing alone may not provide a complete picture of disease risk or prognosis, as other genetic and environmental factors can also influence the development and progression of HUS.

Test Name	CFHR4 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 CFHR4 Gene Hemolytic uremic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFHR4 Gene Hemolytic uremic syndrome NGS Genetic DNA Test gene CFHR4
Test Details	The CFHR4 gene is one of the complement factor H-related genes. Hemolytic uremic syndrome (HUS) is a rare disorder characterized by the destruction of red blood cells, low platelet count, and kidney failure. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup. The CFHR4 gene is associated with atypical hemolytic uremic syndrome (aHUS), which is a form of HUS that is not caused by an infection. Mutations or variations in the CFHR4 gene can lead to abnormal complement regulation, which can trigger the immune system to attack and damage red blood cells, leading to HUS. NGS genetic testing for the CFHR4 gene can help identify mutations or variations in the gene that may contribute to the development of HUS. This information can be used for diagnosis, genetic counseling, and potentially guiding treatment decisions. However, it is important to note that genetic testing alone may not provide a complete picture of disease risk or prognosis, as other genetic and environmental factors can also influence the development and progression of HUS.