Sale!

F9 Gene Thrombophilia X-Linked Due to Factor IX Defect Genetic Test Cost

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

-21%

The “F9 Gene Thrombophilia X-Linked Due to Factor IX Defect Genetic Test” is a specialized diagnostic assessment offered by DNA Labs UAE. This test is designed to detect mutations in the F9 gene, which is responsible for producing Factor IX, a crucial protein for blood clotting. Thrombophilia due to a Factor IX defect is an X-linked condition, meaning it predominantly affects males, though female carriers may also experience symptoms. Mutations in the F9 gene can lead to either an increased risk of bleeding (hemophilia B) or, in rare cases, an increased risk of thrombosis.

At a cost of 4400 AED, the test provides a comprehensive analysis for individuals who have a family history of Factor IX deficiency or have experienced symptoms related to abnormal clotting. By identifying specific genetic alterations in the F9 gene, the test enables healthcare providers to tailor treatment and management plans to the individual’s genetic profile, enhancing the effectiveness of therapy and preventive measures. Conducted at the state-of-the-art facilities of DNA Labs UAE, this genetic test is a critical tool for the accurate diagnosis and management of thrombophilia linked to the F9 gene defect.

Description

F9 Gene Thrombophilia X-linked due to factor IX defect Genetic Test

Genetic testing plays a crucial role in identifying and diagnosing various genetic disorders. One such disorder is F9 Gene Thrombophilia X-linked due to factor IX defect. This disorder affects the blood clotting process and is caused by a defect in the F9 gene.

The F9 gene provides instructions for making a protein called factor IX, which is involved in the clotting cascade. When this gene is defective, it can lead to abnormal blood clotting, increasing the risk of complications such as deep vein thrombosis and pulmonary embolism.

To diagnose F9 Gene Thrombophilia X-linked, a genetic test is conducted using Next-Generation Sequencing (NGS) technology. NGS is a high-throughput DNA sequencing method that allows for the rapid sequencing of large amounts of genetic material. This test analyzes the F9 gene and identifies any mutations or defects that may be present.

The F9 Gene Thrombophilia X-linked genetic test is available at DNA Labs UAE for a cost of AED 4400.0. The test can be performed using a blood sample or extracted DNA. Alternatively, a single drop of blood on an FTA Card can also be used for the test.

The test results are typically delivered within 3 to 4 weeks. Once the results are obtained, they are reviewed by a hematologist, who specializes in the study and treatment of blood disorders. The test is conducted in the genetics department of the lab.

Before undergoing the F9 Gene Thrombophilia X-linked genetic test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by F9 Gene Thrombophilia X-linked. This helps in understanding the inheritance pattern and identifying individuals who may be at risk.

The F9 Gene Thrombophilia X-linked genetic test is not only useful for diagnosing individuals at risk of abnormal blood clotting but also for carrier testing in females. Females who carry the defective gene can pass it on to their children, making carrier testing an important consideration.

Early detection and diagnosis through genetic testing can significantly impact the treatment and management options for individuals with F9 Gene Thrombophilia X-linked. By identifying the presence of mutations or defects, healthcare professionals can develop personalized treatment plans to reduce the risk of complications and improve the overall quality of life for patients.

Genetic testing at DNA Labs UAE provides a comprehensive and accurate assessment of F9 Gene Thrombophilia X-linked due to factor IX defect. The use of NGS technology ensures precise results, enabling healthcare professionals to make informed decisions regarding treatment and management.

Test Name	F9 Gene Thrombophilia X-linked due to factor IX defect 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	Hematology
Doctor	Hematologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for F9 Gene Thrombophilia, X-linked, due to factor IX defect NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F9 Gene Thrombophilia, X-linked, due to factor IX defect NGS Genetic DNA Test gene F9
Test Details	F9 Gene Thrombophilia, X-linked, due to factor IX defect is a genetic disorder that affects the blood clotting process. It is caused by a defect in the F9 gene, which provides instructions for making a protein called factor IX. This protein is involved in the clotting cascade, which helps to stop bleeding by forming blood clots. NGS Genetic Test refers to Next-Generation Sequencing, a high-throughput DNA sequencing technology that can rapidly sequence large amounts of genetic material. In the context of F9 Gene Thrombophilia, X-linked, NGS Genetic Test can be used to analyze the F9 gene and identify any mutations or defects that may be present. The NGS Genetic Test for F9 Gene Thrombophilia, X-linked can help diagnose individuals who may be at risk of developing abnormal blood clotting. It can also be used for carrier testing in females who may pass the defective gene to their children. Early detection and diagnosis through genetic testing can help guide treatment and management options for individuals with this condition.