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 ...

Hereditary spherocytosis (HS) is an inherited condition that affects the red blood cells. The cells are damaged as they pass through the spleen and do not survive as long as normal blood cells.

Hereditary spherocytosis is a rare congenital disorder passed from parents to children. It is usually diagnosed early in life, from infancy to around age 8, when signs of the disease develop.

Examples of cytoskeletal abnormalities include hereditary spherocytosis and elliptocytosis. Anemia occurs when a person has a low number of healthy RBCs. This may happen due to changes in the cell ...

This batch provided an answer: He had hereditary spherocytosis, a disease in which the red blood cells were tiny spheres rather than the usual biconcave discs. This shape makes them much easier to ...

Two conditions that can cause this to happen are called thalassemia and hereditary spherocytosis (HS). These conditions cause the red blood cells to be more likely to break and become a smaller size.

Both she and her father have hereditary spherocytosis and are categorised as being clinically extremely vulnerable, external, making them eligible to get the jab. The World Health Organisation ...

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 ...

Hereditary spherocytosis (HS) is a disorder of the surface, called the membrane, of your red blood cells. It causes your red blood cells to be shaped like spheres instead of flattened discs that ...