HPFH (HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN) 5 DELETION / EDTA BLOOD

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This test detects specific genetic deletions responsible for Hereditary Persistence of Fetal Hemoglobin (HPFH), a condition in which elevated levels of fetal hemoglobin continue into adulthood. It is particularly useful in evaluating unexplained high HbF levels, differentiating HPFH from beta-thalassemia, and assisting in family and reproductive counseling. The test is performed using molecular genetic techniques for precise identification of the 5 common HPFH deletions. Metropolis Healthcare offers highly accurate genetic analysis to support diagnosis and clinical management in individuals with suspected hemoglobin disorders

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Price: Rs. 13,650.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: H0317

Frequently Asked Questions (FAQ's):

What does the HPFH 5 Deletion test detect?
It detects specific genetic deletions linked to Hereditary Persistence of Fetal Hemoglobin.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced molecular genetic methods to identify targeted HPFH deletions accurately.

Who should consider taking this test?
Individuals with elevated HbF levels, suspected hemoglobinopathies, or a family history of thalassemia or related disorders.

What type of sample is required?
A blood sample collected in an EDTA tube.

Do I need to fast before this test?
No fasting or special preparation is required.

Why is this test clinically important?
It helps differentiate HPFH from thalassemia major or intermedia, aiding treatment and counseling decisions.

How long does Metropolis Healthcare take to provide results?
Reports are usually available within 10–14 days depending on analysis complexity.

Is this test helpful for family planning?
Yes, it supports genetic counseling to assess carrier risk in couples planning pregnancy

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