Hereditary spherocytosis
Hereditary spherocytosis
HD - Week 7
HD - Week 7
Blood components
Blood histology
Microcytic anemia: Pathology review
Iron deficiency anemia
Anemia of chronic disease
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Macrocytic anemia: Pathology review
Vitamin B12 deficiency
Non-hemolytic normocytic anemia: Pathology review
Aplastic anemia
Oxygen-hemoglobin dissociation curve
Alpha-thalassemia
Beta-thalassemia
Sickle cell disease (NORD)
Extrinsic hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Autoimmune hemolytic anemia
Warm autoimmune hemolytic anemia and cold agglutinin (NORD)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Disseminated intravascular coagulation
Thrombotic thrombocytopenic purpura
Hereditary spherocytosis
Paroxysmal nocturnal hemoglobinuria
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Key Takeaways
Hereditary spherocytosis (HS) is an autosomal dominant genetic disorder in which red blood cells are sphere-shaped instead of having the normal biconcave shape. These abnormal red blood cells break down prematurely, which can lead to anemia. Also, because of their abnormal shape, red blood cells in spherocytosis don't move through small blood cells efficiently as normal ones do, which can affect tissue oxygenation. People with hereditary spherocytosis can present with jaundice, splenomegaly, and features of anemia like pallor and fatigue.