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F5 Gene Budd-Chiari Syndrome Genetic Test

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

-21%

The F5 Gene Budd-Chiari Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the F5 gene, which have been associated with an increased risk of Budd-Chiari Syndrome (BCS). BCS is a rare vascular disorder characterized by the obstruction of the hepatic veins, which can lead to liver damage, and in severe cases, liver failure. The condition is complex, with genetic factors playing a crucial role in its development alongside environmental influences.

This genetic test is crucial for individuals with a family history of BCS or those exhibiting symptoms related to liver dysfunction, as it can provide valuable insights into their risk of developing this condition. Early detection through genetic testing allows for timely intervention and management strategies to mitigate the risk of severe complications associated with BCS.

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 F5 Gene Budd-Chiari Syndrome Genetic Test is 4400 AED. Given the specialized nature of this test and its potential to significantly impact patient care, it represents a valuable investment in one’s health, particularly for those at increased risk of this syndrome.

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F5 Gene Budd-Chiari Syndrome Genetic Test

Cost: AED 4400.0

Symptoms, Diagnosis, and Test Details

The F5 Gene Budd-Chiari Syndrome Genetic Test is a diagnostic test that uses next-generation sequencing (NGS) technology to detect mutations in the F5 gene associated with Budd-Chiari syndrome. Budd-Chiari syndrome is a rare disorder characterized by the obstruction of the hepatic veins, which can lead to liver damage and failure.

The F5 gene encodes for the coagulation factor V, which is involved in blood clotting. Mutations in the F5 gene can increase the risk of blood clots, contributing to the development of Budd-Chiari syndrome. The NGS technology used in this test allows for the simultaneous analysis of multiple genes, including the F5 gene, in a single test, providing a more comprehensive evaluation of genetic risk factors for Budd-Chiari syndrome.

The F5 Gene Budd-Chiari Syndrome Genetic Test is recommended for individuals with a family history of Budd-Chiari syndrome or those who have experienced unexplained liver damage or blood clots. The results of this test can help guide medical management and treatment decisions.

Test Components and Price

  • Test Name: F5 Gene Budd-Chiari Syndrome Genetic Test
  • 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for F5 Gene Budd-Chiari Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F5 Gene Budd-Chiari Syndrome.

Test Name F5 Gene Budd-Chiari syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for F5 Gene Budd-Chiari syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with F5 Gene Budd-Chiari syndrome
Test Details

The F5 gene Budd-Chiari syndrome NGS genetic test is a diagnostic test that uses next-generation sequencing (NGS) technology to detect mutations in the F5 gene that are associated with Budd-Chiari syndrome. Budd-Chiari syndrome is a rare disorder characterized by the obstruction of the hepatic veins, which can lead to liver damage and failure.

The F5 gene encodes for the coagulation factor V, which is involved in blood clotting. Mutations in the F5 gene can lead to an increased risk of blood clots, which can contribute to the development of Budd-Chiari syndrome.

The NGS technology used in this test allows for the simultaneous analysis of multiple genes, including the F5 gene, in a single test. This can provide a more comprehensive evaluation of genetic risk factors for Budd-Chiari syndrome.

The F5 gene Budd-Chiari syndrome NGS genetic test may be recommended for individuals with a family history of Budd-Chiari syndrome or those who have experienced unexplained liver damage or blood clots. The results of this test can help guide medical management and treatment decisions.