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.

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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 ...

Thalassemia is a rare, inherited blood disorder with limited ... by the FDA in 2022 as the first medicine to treat hemolytic anemia in adults with PK deficiency. Besides this use, the company ...

Background Sickle cell disease (SCD) comprises a heterogeneous group of inherited hemolytic disorders that increases the ... RBC transfusions are commonly used in SCD to treat severe anemia and to ...

Accumulation of clots causes some of the most severe symptoms of sickle cell disease, including strokes, kidney failure, ...

The largest study to date to analyze millions of both genetic and patient records on the long-term health conditions of later ...

July 25, 2024 — In a rigorous medical records study covering tens of thousands of patients, researchers conclude that some patients with preoperative anemia have better outcomes if they get iron ...

At the age of 20, Prince Karim Al-Hussaini inherited the reins of a Shia Muslim lineage and used his entrepreneurship to become one of the world’s richest hereditary rulers. By Alan Cowell The ...

Among the immediate complications of transfusion, the most common and serious are intravascular hemolytic transfusion reactions because of ABO incompatibility caused by giving the wrong blood to a ...