CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test
Welcome to DNA Labs UAE, where we offer the CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test. This test is designed to diagnose and understand the underlying causes of hemolytic uremic syndrome (HUS), a rare disorder characterized by the destruction of red blood cells, low platelet count, and kidney failure.
Test Details
The CFHR1 gene is associated with HUS. Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously, helping us identify mutations or variations in the CFHR1 gene that may be contributing to the development of the condition. By understanding these genetic variations, our healthcare providers can develop targeted treatments or interventions.
Test Components and Price
Our CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test is priced at AED 4400.0. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. Our method utilizes NGS technology, ensuring accurate and reliable results.
Test Type and Doctor
The CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test falls under the categories of Hepatology, Nephrology, and Endocrinology Disorders. It is recommended to consult with a General Physician who specializes in Genetics.
Pre Test Information
Before undergoing the CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counseling session may be conducted to draw a pedigree chart of family members affected by the CFHR1 gene. This information will assist in accurate interpretation of the test results.
Please note that NGS genetic testing is a complex and specialized procedure that should be performed in specialized laboratories. It should be ordered by a healthcare provider who suspects a genetic cause for the patient’s condition. The results of the test should be interpreted by a qualified healthcare professional familiar with the patient’s medical history and clinical presentation.
At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule your CFHR1 Gene Hemolytic Uremic Syndrome Genetic Test.
| Test Name | CFHR1 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 CFHR1 Gene Hemolytic uremic syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFHR1 Gene Hemolytic uremic syndrome NGS Genetic DNA Test gene CFHR1 |
| Test Details |
The CFHR1 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 can be caused by genetic mutations, infections, or certain medications. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify mutations or variations 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 CFHR1 gene that may be contributing to the development of the condition. By identifying these genetic variations, healthcare providers can better understand the underlying cause of the disease and potentially develop targeted treatments or interventions. NGS genetic testing can also be used for diagnostic purposes, to confirm a suspected diagnosis of hemolytic uremic syndrome based on clinical symptoms. It is important to note that NGS genetic testing is a complex and specialized procedure that requires expertise in genetic analysis and interpretation. It is typically performed in specialized laboratories and may be ordered by a healthcare provider who suspects a genetic cause for a patient’s condition. The results of NGS genetic testing should be interpreted by a qualified healthcare professional familiar with the patient’s medical history and clinical presentation. |
