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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. In hereditary spherocytosis, your red blood cells lose their characteristic disk-like shape, becoming round, or spherical cells (spherocytes), that can’t function like normal red ...

  2. 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 ...

  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] 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
  4. 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 enlarged ...

  5. Jan 1, 2024 · Hereditary spherocytosis (HS) is an inherited condition that affects your red blood cells. The red blood cells are those that carry oxygen around the body. Their shape (like a slightly elongated saucer) helps them carry oxygen effectively. In HS there is a defect in the outer layer of the red blood cell. This means the cell is not the usual shape.

  6. Mar 15, 2023 · Hereditary spherocytosis is the predominant cause of spherocytosis and is caused by several genetic mutations that lead to membrane abnormalities of red blood cells. The disease usually is inherited as an autosomal dominant trait; although a few people with hereditary spherocytosis may develop it secondary to new mutations.

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  8. 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. This abnormal shape interferes with the cells' ability to flex during blood circulation ...

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