Sickle Cell Anemia

Sickle Cell Anemia

TL;DR Sickle cell anemia is a hereditary chronic hemolytic anemia caused by the production of Hb S (a qualitative hemoglobin defect due to a β-globin gene codon 6 mutation [glutamic acid → valine]). Pathophysiology ▾: Sickle cell anemia is a...
Beta Thalassemia

Beta Thalassemia

TL;DR Beta thalassemia is a hereditary hemoglobin disorder due to reduced or absence of beta-globin chain production leading to ineffective erythropoiesis and anemia. It is predominantly an autosomal recessive gene disorder. Classifications CharacteristicBeta...
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