F13B Gene Factor XIIIB deficiency Genetic Test sale cost 4400 AED
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F13B Gene Factor XIIIB deficiency Genetic Test Cost

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

-21%

The F13B gene factor XIIIB deficiency genetic test is a specialized diagnostic procedure aimed at detecting deficiencies in the Factor XIII B subunit, a crucial protein involved in blood clotting. This test specifically examines the F13B gene for mutations or alterations that could lead to Factor XIII deficiency, a rare genetic disorder that can cause severe bleeding problems. The test is crucial for individuals who have a family history of the disorder or exhibit symptoms related to abnormal bleeding, as early detection can significantly improve management and treatment outcomes.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures accuracy and reliability through advanced genomic technologies. The cost of the test is 4400 AED, reflecting the sophisticated nature of the testing process and the specialized expertise required to interpret the results. By identifying specific genetic alterations in the F13B gene, this test plays a pivotal role in guiding clinical decisions, enabling personalized treatment plans, and providing valuable information for family planning to those affected by or at risk of Factor XIII B subunit deficiency.

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F13B Gene Factor XIIIB deficiency Genetic Test

Test Name: F13B Gene Factor XIIIB deficiency Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for F13B Gene Factor XIIIB deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Factor XIIIB deficiency.

Test Details

F13B gene factor XIIIB deficiency is a rare genetic disorder characterized by a deficiency of factor XIIIB, a blood clotting protein. This deficiency can lead to abnormal bleeding and clotting tendencies in affected individuals.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes. In the case of F13B gene factor XIIIB deficiency, NGS genetic testing can be used to identify any mutations or variations in the F13B gene that may be responsible for the deficiency. NGS testing involves sequencing the entire F13B gene or specific regions of interest to identify any genetic changes.

This can help in diagnosing individuals with factor XIIIB deficiency and also in identifying carriers of the gene mutation. NGS genetic testing can provide valuable information for affected individuals and their families, including a definitive diagnosis, risk assessment, and genetic counseling. It can also aid in the development of targeted treatment strategies and management plans for individuals with F13B gene factor XIIIB deficiency.

Test Name F13B Gene Factor XIIIB 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for F13B Gene Factor XIIIB deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Factor XIIIB deficiency
Test Details

F13B gene factor XIIIB deficiency is a rare genetic disorder characterized by a deficiency of factor XIIIB, a blood clotting protein. This deficiency can lead to abnormal bleeding and clotting tendencies in affected individuals.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes. In the case of F13B gene factor XIIIB deficiency, NGS genetic testing can be used to identify any mutations or variations in the F13B gene that may be responsible for the deficiency.

NGS testing involves sequencing the entire F13B gene or specific regions of interest to identify any genetic changes. This can help in diagnosing individuals with factor XIIIB deficiency and also in identifying carriers of the gene mutation.

NGS genetic testing can provide valuable information for affected individuals and their families, including a definitive diagnosis, risk assessment, and genetic counseling. It can also aid in the development of targeted treatment strategies and management plans for individuals with F13B gene factor XIIIB deficiency.

SKU: TEST-2303 Category:

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