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F12 Gene Factor XII Deficiency Genetic Test

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

-21%

The F12 Gene Factor XII Deficiency Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the F12 gene, which is responsible for the production of Factor XII, a critical component in the blood clotting process. Factor XII deficiency, also known as Hageman factor deficiency, is a rare genetic disorder that can lead to an increased risk of bleeding or, paradoxically, form blood clots in some cases.

This test is crucial for individuals who have a family history of clotting disorders or have experienced unexplained symptoms related to abnormal clotting or bleeding. By analyzing a sample of the patient’s DNA, the test can confirm the presence of mutations in the F12 gene, providing essential information for the diagnosis, treatment, and management of the condition.

The cost of the F12 Gene Factor XII Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the F12 gene. Patients undergoing this test at DNA Labs UAE can expect comprehensive support, from sample collection through to the interpretation of results, ensuring they receive the most accurate and helpful information regarding their genetic health.

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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F12 Gene Factor XII deficiency Genetic Test

Are you concerned about Factor XII deficiency? DNA Labs UAE offers a comprehensive and accurate F12 gene Factor XII deficiency genetic test using Next-Generation Sequencing (NGS) technology. This test can help identify mutations or variations in the F12 gene that may be associated with Factor XII deficiency.

Test Components and Price

  • Test Name: F12 Gene Factor XII deficiency Genetic Test
  • Price: 4400.0 AED

Sample Condition and Report Delivery

You can provide a blood sample, extracted DNA, or even one drop of blood on an FTA card for this test. The report will be delivered to you within 3 to 4 weeks.

Method and Test Type

We use NGS technology for the F12 gene Factor XII deficiency genetic test. This technology allows us to analyze multiple genes simultaneously, making it a powerful tool for genetic testing. The test falls under the Hepatology, Nephrology, and Endocrinology Disorders category.

Test Department and Doctor

  • Test Department: Genetics
  • Doctor: General Physician

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who will undergo the F12 gene Factor XII deficiency NGS genetic DNA test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the F12 gene Factor XII deficiency.

Test Details

The F12 gene Factor XII deficiency NGS genetic test analyzes the F12 gene for mutations or variations that may be associated with Factor XII deficiency. This rare genetic disorder is characterized by a deficiency or dysfunction of factor XII, a blood clotting protein. The test helps identify any disruptions in the production or function of factor XII due to mutations in the F12 gene.

The NGS genetic test for F12 gene Factor XII deficiency provides valuable information for diagnosis, risk assessment, and genetic counseling. It can detect both known and novel mutations in the gene, enabling healthcare professionals to make informed decisions regarding patient management and treatment.

It is important to note that the F12 gene Factor XII deficiency NGS genetic test should be ordered and interpreted by a qualified healthcare professional or genetic counselor. They will consider the individual’s clinical presentation, family history, and other relevant factors to determine the appropriate genetic testing strategy and provide appropriate counseling and support.

Test Name F12 Gene Factor XII deficiency 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 F12 Gene Factor XII deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with F12 Gene Factor XII deficiency NGS Genetic DNA Test gene F12
Test Details

F12 gene factor XII deficiency NGS genetic test is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the F12 gene for mutations or variations that may be associated with factor XII deficiency.

Factor XII deficiency is a rare genetic disorder characterized by a deficiency or dysfunction of factor XII, a blood clotting protein. This deficiency can lead to an increased risk of abnormal blood clotting or bleeding episodes.

The F12 gene provides instructions for making factor XII. Mutations in this gene can disrupt the production or function of factor XII, leading to factor XII deficiency.

The NGS genetic test for F12 gene factor XII deficiency involves sequencing the DNA of an individual to identify any variations or mutations in the F12 gene. This test can detect both known and novel mutations in the gene, providing valuable information for diagnosis, risk assessment, and genetic counseling.

NGS technology allows for the analysis of multiple genes simultaneously, making it a powerful tool for genetic testing. It provides a comprehensive and accurate assessment of the F12 gene, enabling healthcare professionals to make informed decisions regarding patient management and treatment.

It is important to note that the F12 gene factor XII deficiency NGS genetic test should be ordered and interpreted by a qualified healthcare professional or genetic counselor. They will consider the individual’s clinical presentation, family history, and other relevant factors to determine the appropriate genetic testing strategy and provide appropriate counseling and support.