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THBD Gene Hemolytic Uremic Syndrome Genetic Test Cost

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

-21%

The THBD Gene Hemolytic Uremic Syndrome Genetic Test is a specific diagnostic tool available at DNA Labs UAE, designed to identify mutations in the THBD gene, which are associated with an increased risk of developing Hemolytic Uremic Syndrome (HUS). HUS is a rare but severe condition characterized by the triad of acute renal failure, microangiopathic hemolytic anemia, and thrombocytopenia. This condition often arises following an infection, particularly by certain strains of E. coli, but when linked to genetic factors like mutations in the THBD gene, it can present without a preceding infection, leading to atypical HUS.

The test, priced at 4400 AED, involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory to detect any genetic anomalies in the THBD gene. The outcome of this test can significantly influence the management and treatment plan for individuals at risk of or presenting with symptoms of HUS. Early detection through genetic testing allows for timely intervention, potentially mitigating severe complications associated with the disease. DNA Labs UAE offers this specialized genetic test as part of its comprehensive suite of diagnostic services, employing state-of-the-art technology and expertise to ensure accurate and reliable results.

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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THBD Gene Hemolytic Uremic Syndrome Genetic Test

Test Name: THBD Gene Hemolytic Uremic Syndrome Genetic Test

Components: Thrombomodulin protein

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

Test Details

The THBD gene is responsible for encoding the thrombomodulin protein, which plays a crucial role in regulating blood coagulation and preventing abnormal clot formation. Hemolytic uremic syndrome (HUS) is a rare condition characterized by the destruction of red blood cells, kidney failure, and low platelet count.

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of HUS, NGS genetic testing can be used to identify mutations or variations in the THBD gene that may be associated with the development of the condition. This information can help in diagnosing individuals with HUS and potentially guide treatment decisions.

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

The THBD gene is responsible for encoding the thrombomodulin protein, which plays a crucial role in regulating blood coagulation and preventing abnormal clot formation. Hemolytic uremic syndrome (HUS) is a rare condition characterized by the destruction of red blood cells, kidney failure, and low platelet count.

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the context of HUS, NGS genetic testing can be used to identify mutations or variations in the THBD gene that may be associated with the development of the condition. This information can help in diagnosing individuals with HUS and potentially guide treatment decisions.