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

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  3. 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]

    • Edgar A. Zamora, Catherine A. Schaefer
    • 2023/07/04
  4. Oct 25, 2023 · 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 lipid bilayer.

  5. Jun 9, 2018 · This breakdown process is called hemolytic anemia. A normal red blood cell can live for up to 120 days, but red blood cell with hereditary spherocytosis might live for as few as 10 to 30 days.

    • Carmella Wint
  6. Hereditary spherocytosis (HS) is a congenital hemolytic disorder wherein a genetic mutation coding for a structural membrane protein phenotype causes the red blood cells to be sphere-shaped (spherocytosis), rather than the normal biconcave disk shape.

  7. 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).

  8. Oct 24, 2021 · Hereditary spherocytosis (HS) is a hereditary hemolytic anemia caused by the mutations in the genes encoding erythrocyte membrane proteins and is mostly inherited in an autosomal dominant manner. , , HS is classified into four types according to the severity of the disease: trait, mild, moderate, and severe.

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