48+ Hereditary Spherocytosis Vs Sickle Cell Anemia PNG
48+ Hereditary Spherocytosis Vs Sickle Cell Anemia PNG. The splenic hypofunction and fibrosis as a result of sickling has ameliorated the clinical course of the 35 year old father. Most individuals with hs have moderate disease.
Following thalassemia syndrome and sickle cell disease (scd), hereditary spherocytosis (hs) is the most common form of congenital hemolytic anemia with an incidence of approximately 1:2000 and a table 2.indications for splenectomy in hereditary spherocytosis based on severity of disease*.
Defects in specific cause of hemolytic anemia. This shortage of erythrocytes results in hemolytic anemia. A splenectomy was performed, and following surgery the hemoglobin concentration was maintained between 9 and 11 g/dl without further transfusion requirements. Stomatocytosis and anemia caused by hypophosphatemia.
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