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  1. May 19, 2022 · Hereditary spherocytosis is a rare inherited disorder that requires lifelong medical care. Healthcare providers can treat the sometimes-serious medical conditions that hereditary spherocytosis causes. They can’t cure the blood disorder, though. It’s not always easy to have a chronic illness or care for someone who does.

  2. Feb 14, 2024 · Hereditary spherocytosis is a disorder in which the red blood cells are abnormal and fragile. Learn about the causes, symptoms, and treatment options for this disorder today.

  3. Feb 16, 2022 · Treatment. Spherocytosis is a condition that causes a person’s red blood cells to be shaped like spheres (round balls) instead of their normal disk shape. It can cause symptoms of anemia (lack of healthy red blood cells) and an enlarged spleen (an organ that filters and stores blood). This condition is usually inherited.

  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. It is a result of heterogeneous alterations in one of five genes that encode red blood cell (RBC) membrane proteins involved in vertical associations that link the membrane cytoskeleton to the ...

  5. Jul 4, 2023 · Hereditary spherocytosis (HS) is the most prevalent cause of hemolytic anemia due to an abnormal red cell membrane and classifies as a type of congenital hemolytic anemia. Oskar Minkowsky first described it in the early 1900s.[1] Erythrocytes are unable to maintain their normal biconcave shape due to genetic mutations in membrane/cytoskeletal proteins that play a role in structural morphologic ...

    • Edgar A. Zamora, Catherine A. Schaefer
    • 2023/07/04
  6. Mar 6, 2023 · Spherocytosis increases the risk of certain serious symptoms, most notably hemolytic anemia. It is important to seek treatment for any new symptoms and consult with a doctor about strategies to ...

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  8. Mar 22, 2023 · Hereditary spherocytosis (HS) is a familial hemolytic disorder associated with a variety of mutations that lead to defects in red blood cell (RBC) membrane proteins. The morphologic hallmark of HS is the microspherocyte, which is caused by loss of RBC membrane surface area and has abnormal osmotic fragility in vitro.

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