Bilirubin tests: A high level of unconjugated bilirubin compared to levels of conjugated bilirubin suggest hemolytic jaundice. Full blood count (FBC), or complete blood count (CBC): This measures levels of red blood cells, white blood cells, and platelets.

Treatment of the condition is specific to the cause of hemolysis, but intense phototherapy and exchange transfusion can be used to help the patient excrete accumulated bilirubin.

How is Jaundice diagnosed? To diagnose jaundice, your doctor will take your child’s medical history and conduct a physical exam. A diagnostic blood test may also be performed to check for hepatitis virus antibodies, bilirubin levels, abnormal red blood cells and other substances that indicate liver function.

Diagnosis of Hemolytic Anemia. Hemolysis is suspected in patients with anemia and reticulocytosis. If hemolysis is suspected, a peripheral smear is examined and serum bilirubin, LDH, haptoglobin, and ALT are measured. The peripheral smear and reticulocyte count are the most important tests to diagnose hemolysis.

To diagnose hemolytic anemia, your doctor will do a physical exam and order blood tests. Additional tests may include a urine test, a bone marrow test, or genetic tests.

Hemolytic jaundice, congenital: Known also as hereditary spherocytosis (HS), this is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen). In HS the red cells are smaller, rounder, and more fragile than normal.

Infants with HDN may be treated with: Feeding often and receiving extra fluids. Light therapy (phototherapy) using special blue lights to convert bilirubin into a form which is easier for the baby’s body to get rid of.

Urinalysis (urine testing) that’s positive for bilirubin shows that the patient has conjugated jaundice. The findings of urinalysis should be confirmed by serum testing. The serum testing will include a complete blood count (CBC) and bilirubin levels.

Hemolytic jaundice, congenital: Known also as hereditary spherocytosis (HS), this is a genetic disorder of the red blood cell membrane clinically characterized by anemia, jaundice (yellowing) and splenomegaly (enlargement of the spleen). In HS the red cells are smaller, rounder, and more fragile than normal.

Signs and Symptoms of 6 Types of Anemia Blood Disease Pernicious Anemia (PA) Hemolytic Anemia (HA) Sickle Cell Anemia (SCA) Aplastic Anemia (AA) Fanconi Anemia (FA) Bone Marrow Disease Anemia

High total bilirubin that is mostly unconjugated (indirect) may be caused by: Strenuous exercise can increase your bilirubin levels. Anemia. Cirrhosis. A reaction to a blood transfusion. Gilbert syndrome — a common, inherited condition in which there is a deficiency of an enzyme that helps to break down bilirubin.

Acute hepatitis c. Acute Hepatitis C is a liver inflammation caused by Hepacivirus C.