Short Description

Hereditary persistence of fetal hemoglobin (HPFH) is performed using End Point PCR methodology. Sample that have to be given is Amniotic fluid / Chorionic villi / Cord blood in Sterile container / Sterile Normal Saline Container / EDTA Vacutainer (2ml) for this test. You can expect results in 7-8 days

PreTest Information

Hereditary persistence of fetal hemoglobin (HPFH) can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.

Detail Description

Understanding Hereditary Persistence of Fetal Hemoglobin (HPFH)

Hereditary Persistence of Fetal Hemoglobin (HPFH) is a rare genetic condition that affects the production of hemoglobin. Hemoglobin is a protein found in red blood cells that carries oxygen throughout the body. In individuals with HPFH, the production of fetal hemoglobin (HbF) continues into adulthood, instead of being replaced by adult hemoglobin (HbA) as it normally would. This results in higher levels of HbF in the blood.

Symptoms of HPFH

Most individuals with HPFH do not experience any symptoms. However, in some cases, individuals may experience mild anemia or jaundice. Anemia is a condition in which there are not enough red blood cells to carry oxygen throughout the body. Jaundice is a condition in which the skin and eyes appear yellow due to high levels of bilirubin, a byproduct of the breakdown of red blood cells.

Diagnosis of HPFH

HPFH is typically diagnosed through a blood test that measures the levels of HbF in the blood. If the levels of HbF are higher than normal, genetic testing may be performed to confirm the diagnosis.

Treatment for HPFH

There is no cure for HPFH. Treatment is typically focused on managing any symptoms that may be present. In some cases, blood transfusions may be necessary to treat severe anemia.

The Cost of HPFH Testing in India

At DNA Labs India, we offer HPFH testing for a cost of INR 6000. Our testing is performed using the latest technology and equipment, ensuring accurate and reliable results.

Conclusion

HPFH is a rare genetic condition that affects the production of hemoglobin. While most individuals with HPFH do not experience any symptoms, some may experience mild anemia or jaundice. Diagnosis is typically performed through a blood test that measures the levels of HbF in the blood, with genetic testing used to confirm the diagnosis. Treatment is focused on managing any symptoms that may be present. At DNA Labs India, we offer HPFH testing for a cost of INR 6000, using the latest technology and equipment to ensure accurate and reliable results.

If you suspect that you or a loved one may have HPFH, we encourage you to speak with a healthcare professional to discuss testing options.

For more information on HPFH testing or any of our other genetic testing services, please contact DNA Labs India today.