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Requisites
Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days for obtaining the report for the test Haemophilia (F8 & F9) Gene Panel is 14 days.

What are the prerequisites for the test Haemophilia (F8 & F9) Gene Panel

  • Patients must have a suspected or confirmed diagnosis of haemophilia.
  • Patients must have a family history of haemophilia.
  • Patients must not be on any anticoagulant therapy at the time of testing.
  • Patients must not have received any blood transfusions in the past 3 months.

What are the measure values for the test Haemophilia (F8 & F9) Gene Panel

  • F8 Gene Panel:
    • Factor VIII Activity (FVIII:C) - Normal Range: 50-150%
    • Factor VIII Antigen (FVIII:Ag) - Normal Range: 50-150%
    • F8 Gene Sequencing - Detection of mutations in the F8 gene
    • F8 Gene Deletion/Duplication Analysis - Detection of large deletions or duplications in the F8 gene
  • F9 Gene Panel:
    • Factor IX Activity (FIX:C) - Normal Range: 50-150%
    • Factor IX Antigen (FIX:Ag) - Normal Range: 50-150%
    • F9 Gene Sequencing - Detection of mutations in the F9 gene
    • F9 Gene Deletion/Duplication Analysis - Detection of large deletions or duplications in the F9 gene

What does this test Haemophilia (F8 & F9) Gene Panel identify?

  • This test identifies mutations in the F8 gene and F9 gene, which are responsible for causing Haemophilia A and B, respectively.
  • Haemophilia A is a genetic disorder caused by mutations in the F8 gene, leading to a deficiency in clotting factor VIII.
  • Haemophilia B is caused by mutations in the F9 gene, resulting in a deficiency of clotting factor IX.
  • By analyzing the F8 and F9 genes, this test can identify specific mutations that may be causing the Haemophilia phenotype in an individual.

Why is this test Haemophilia (F8 & F9) Gene Panel taken?

Haemophilia (F8 & F9) Gene Panel test is taken to diagnose and confirm the presence of mutations in the F8 and F9 genes, which are responsible for causing hemophilia A and hemophilia B respectively. Hemophilia is a genetic disorder that impairs the body's ability to control blood clotting, leading to excessive bleeding and bruising.

By analyzing the F8 and F9 genes, healthcare providers can identify specific mutations that may be causing the hemophilia and tailor treatment plans accordingly. This test is particularly important for individuals with a family history of hemophilia or those who exhibit symptoms such as prolonged bleeding after injury or surgery.

Overall, the Haemophilia (F8 & F9) Gene Panel test helps in the accurate diagnosis, management, and genetic counseling of individuals affected by hemophilia, ultimately improving their quality of life and reducing the risk of complications associated with the disorder.

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