These findings are similar to those commonly noted in hereditary spherocytosis and do not conform to either the Type 1 or the Type 2 pattern of congenital nonspherocytic hemolytic anemia.

Hereditary spherocytosis (HS) is a genetic condition that leads to hemolytic anemia, a disorder where red blood cells are destroyed faster than they can be made. This condition is characterized by ...

Deficient activity of erythrocyte and leukocyte glucosephosphate isomerase was found in three siblings with hereditary hemolytic anemia who were unrelated to the single patient previously described.

These tests may include genetic tests or diagnostic procedures ... In some cases, blood transfusions may benefit people who have hemolytic anemia. Blood transfusions can restore a normal RBC ...

Expresses differences in erythrocyte size in an individual specimen Used to detect anisocytosis. Increased in immune hemolytic anemia, SS and SC disease, and hereditary spherocytosis ...

"By linking specific genetic variants ... they encounter a case with anemia and abnormal iron profile suggestive of iron ...

Favism is a sex-linked, inherited condition that results from ... when affected individuals eat fava beans, they develop hemolytic anemia, a condition in which red blood cells break apart and ...

Children with sickle cell disease, a chronic hemolytic anemia, present with a wide variety ... Sickle cell disease (SCD) is a group of recessively inherited hemoglobinopathies common among people ...