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F2 Gene Dysprothrombinemia Genetic Test Cost

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

-21%

The F2 Gene Dysprothrombinemia Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the F2 gene, which is responsible for the production of prothrombin (factor II) – a protein crucial for blood clotting. Dysprothrombinemia is a rare coagulation disorder characterized by abnormal blood clotting, which can lead to either excessive bleeding or thrombosis, depending on the nature of the mutation. The test is crucial for individuals with a family history of coagulation disorders or those exhibiting symptoms related to abnormal clotting. It involves analyzing the patient’s DNA to detect specific genetic variations associated with the condition, providing valuable information for diagnosis, management, and treatment planning. The cost of the F2 Gene Dysprothrombinemia Genetic Test at DNA Labs UAE is 4400 AED, reflecting the comprehensive nature of the analysis and the expertise required to interpret the results accurately.

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F2 Gene Dysprothrombinemia Genetic Test

Welcome to the DNA Labs UAE blog! Today, we will be discussing the F2 Gene Dysprothrombinemia Genetic Test, its cost, symptoms, diagnosis, and other important details.

Test Name: F2 Gene Dysprothrombinemia Genetic Test

Components: This test analyzes the F2 gene for mutations associated with dysprothrombinemia.

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: Hematology

Doctor: Hematologist

Test Department: Genetics

Pre Test Information

Prior to taking the F2 Gene Dysprothrombinemia NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by F2 Gene Dysprothrombinemia.

Test Details

The F2 gene dysprothrombinemia NGS genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the F2 gene for mutations associated with dysprothrombinemia. Dysprothrombinemia is a rare inherited blood disorder characterized by abnormal clotting factors in the blood.

The F2 gene, also known as the prothrombin gene, plays a crucial role in blood clotting. Mutations in the F2 gene can result in dysprothrombinemia, leading to either increased or decreased levels of prothrombin.

The NGS genetic test examines the DNA sequence of the F2 gene to identify any mutations or variations. This test aids in the diagnosis of dysprothrombinemia and determines the specific genetic cause of the condition.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive genetic profile. This test is beneficial for individuals with a family history of dysprothrombinemia or those experiencing symptoms related to the condition. It can also be used for carrier testing in individuals who may be at risk of passing the condition on to their children.

In summary, the F2 gene dysprothrombinemia NGS genetic test offers valuable information about the genetic basis of dysprothrombinemia. It assists in diagnosis, risk assessment, and genetic counseling.

Test Name F2 Gene Dysprothrombinemia 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 F2 Gene Dysprothrombinemia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F2 Gene Dysprothrombinemia NGS Genetic DNA Test gene F2
Test Details

F2 gene dysprothrombinemia NGS genetic test is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the F2 gene for mutations associated with dysprothrombinemia.

Dysprothrombinemia is a rare inherited blood disorder characterized by abnormal clotting factors in the blood. The F2 gene, also known as the prothrombin gene, provides instructions for making a protein called prothrombin, which is involved in blood clotting. Mutations in the F2 gene can lead to dysprothrombinemia, causing either increased or decreased levels of prothrombin.

The NGS genetic test analyzes the DNA sequence of the F2 gene to identify any mutations or variations that may be present. This can help diagnose dysprothrombinemia and determine the specific genetic cause of the condition.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive genetic profile. This test can be useful for individuals with a family history of dysprothrombinemia or those who have symptoms suggestive of the condition. It can also be used for carrier testing in individuals who may be at risk of passing the condition on to their children.

Overall, the F2 gene dysprothrombinemia NGS genetic test provides valuable information about the genetic basis of dysprothrombinemia, aiding in diagnosis, risk assessment, and genetic counseling.

SKU: TEST-3897 Category:

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