HAEMOPHILIA B (F9) GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited   
The Haemophilia B (F9) Gene Panel by NGS is a specialized genetic test designed to detect mutations in the F9 gene, which are responsible for Haemophilia B—an inherited bleeding disorder caused by reduced Factor IX activity. Affected individuals may experience prolonged bleeding, easy bruising, joint bleeds, and delayed clotting after injury or surgery. Using an EDTA blood sample, this test is performed through advanced Next Generation Sequencing for precise variant detection. Metropolis Healthcare offers accurate and reliable results to support diagnosis, treatment planning, and genetic counseling for families

  • 17 Crores+ Samples Processed
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  • Free Home Collection

Price: Rs. 19,950.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0120

Frequently Asked Questions (FAQ's):

What is Haemophilia B?
Haemophilia B is a genetic bleeding disorder caused by Factor IX deficiency, leading to prolonged or excessive bleeding.

Why is the F9 gene analyzed in this test?
Mutations in the F9 gene directly cause Haemophilia B, making genetic testing essential for confirmation and family screening.

How does Metropolis Healthcare conduct this test?
Metropolis Healthcare uses advanced NGS technology to identify mutations in the F9 gene with high accuracy.

What type of sample is needed?
An EDTA whole blood sample is required.

Who should consider this test?
Individuals with unexplained bleeding, a family history of Haemophilia B, or prolonged clotting issues may benefit from this test.

Is any preparation required before giving the sample?
No special preparation or fasting is needed.

How long do results take at Metropolis Healthcare?
Results are typically available within a few working days depending on laboratory workflow.

How will the results help?
They confirm diagnosis, guide treatment decisions, and support genetic counseling for affected families

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