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  1. May 19, 2022 · Overview. What is hereditary spherocytosis? Hereditary spherocytosis is an inherited blood disorder that causes hemolytic anemia. This anemia happens when your red blood cells break down faster than normal.

  2. Jul 4, 2023 · Hereditary spherocytosis, a type of congenital hemolytic anemia, is the most prevalent cause of hemolytic anemia due to an abnormal red cell membrane. These atypical erythrocytes are unable to maintain their normal biconcave shape due to genetic mutations in the membrane/cytoskeletal proteins that play a role in structural morphologic stability.

    • Edgar A. Zamora, Catherine A. Schaefer
    • 2023/07/04
  3. Feb 14, 2024 · Hereditary spherocytosis is a genetic disorder in which the red blood cells (RBCs) are fragile and burst easily. These disc-shaped cells, which have a lifespan of 120 days, contain hemoglobin and...

  4. Oct 25, 2023 · INTRODUCTION. Although relatively rare, hereditary spherocytosis (HS) is the most common cause of hemolytic anemia due to a red cell membrane defect.

  5. Mar 6, 2023 · Hereditary or congenital spherocytosis is an inherited condition where the red blood cells are spherical instead of the usual disk shape. It can lead to jaundice, hemolytic anemia, and an...

  6. Jan 1, 2024 · Hereditary spherocytosis (HS) is an inherited condition of red blood cells. The disease can be mild and go unrecognised in some people. In others there may be severe anaemia requiring regular blood transfusions. Some people with hereditary spherocytosis may be offered surgery to remove their spleen.

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  8. Aug 5, 2019 · Hereditary spherocytosis (HS) is an inherited disease that affects the red blood cells. Characteristic symptoms of HS are the destruction of red blood cells in the spleen and their removal from the blood stream (hemolytic anemia), a yellow tone to the skin (jaundice), and an enlarged spleen (splenomegaly).