HB Electrophoresis is a diagnostic test that separates and identifies different types of hemoglobin in the blood to diagnose hemoglobin disorders.

This test is used to diagnose conditions like sickle cell disease and thalassemia, monitor disease progression, and screen for hemoglobin disorders.

No special preparation is needed. You can eat and drink normally, but inform your healthcare provider about any medications or health conditions.

Results are typically available within 2 to 3 days after the test.

The results provide information on the different types of hemoglobin present and their quantities, helping to diagnose and manage hemoglobin disorders and genetic conditions.

The procedure typically lasts between 4 to 6 hours, depending on the complexity of the surgery and the number of electrodes implanted.

Symptoms may include confusion, fatigue, weakness, and in severe cases, coma.

Treatment involves reducing ammonia levels through medications and dietary changes.

Yes, certain medications, especially those metabolised by the liver, can influence ammonia levels.

Liver disease, kidney dysfunction, and urea cycle disorders can impact ammonia metabolism.

A blood sample is drawn from a vein in the arm and sent to a laboratory for analysis.