HAEMOPHILIA A GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited   
The Haemophilia A Gene Panel by NGS is a specialized genetic test designed to detect mutations in the F8 gene, the primary cause of Haemophilia A. This inherited bleeding disorder leads to reduced Factor VIII activity, resulting in easy bruising, prolonged bleeding, and recurrent joint bleeds. The test is performed on an EDTA blood sample using advanced Next Generation Sequencing to ensure accurate identification of disease-causing variants. Metropolis Healthcare provides precise and dependable results that support diagnosis, treatment planning, and essential family counseling

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 19,950.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0119

Frequently Asked Questions (FAQ's):

What is Haemophilia A?
Haemophilia A is a genetic disorder caused by Factor VIII deficiency, leading to abnormal or prolonged bleeding.

Why is the F8 gene tested?
Mutations in the F8 gene cause Haemophilia A, making this gene essential for diagnostic confirmation and family screening.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-accuracy Next Generation Sequencing to identify mutations in the F8 gene.

What sample is required for this test?
An EDTA whole blood sample is needed.

Who should consider this test?
Individuals with a family history of Haemophilia A or those experiencing unexplained bleeding or frequent joint bleeds may benefit from this test.

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

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

How do the results help?
They confirm diagnosis, guide appropriate treatment strategies, and support genetic counseling for families

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