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Congenital genetic condition
- Hereditary spherocytosis is a congenital genetic condition. This means that it is present at birth and that mutations in genes cause it. There is no evidence that anything that happens after birth can result in this condition. A deficiency in at least one protein that gives red blood cells their shape leads to this condition.
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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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Hereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells ( anemia ), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly).
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
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,...
Feb 16, 2022 · Spherocytosis is a red blood cell disorder that is usually inherited. It is a lifelong disease that causes red blood cells to be susceptible to excessive hemolysis (breakdown) due to a defect in the membranes of the red blood cells.
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.
2 days ago · Hereditary spherocytosis is an inherited abnormality of the red blood cell, caused by defects in structural membrane proteins. It is the most common form of inherited haemolytic anaemia in the US and northern Europe.