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  1. May 19, 2022 · Treatment varies depending on symptoms. For example, newborns who have severe anemia may receive blood transfusions and/or erythropoietin-stimulating agents (ESA) as soon as healthcare providers diagnose hereditary spherocytosis.

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  3. Feb 14, 2024 · What Is the Treatment for Hereditary Spherocytosis? Treatment for this disorder depends on its severity. If you have a mild form of hereditary spherocytosis, your doctor will likely recommend ...

  4. Mar 6, 2023 · Treatment. In most people, splenectomy — or removal of the spleen — can cure symptoms. However, this procedure can increase the risk of serious infections and pose other surgery-related risks...

  5. Aug 5, 2019 · Programs & Resources. Assistance Programs. Patient Organizations. More Information. RareCare ® Assistance Programs. Additional Assistance Programs. Learn about Hereditary Spherocytosis, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find.

  6. View Patient Education. Pathophysiology |. Symptoms and Signs |. Diagnosis |. Treatment. Hereditary spherocytosis and hereditary elliptocytosis are congenital red blood cell (RBC) membrane disorders that can cause a mild hemolytic anemia.

  7. 2 days ago · Splenectomy is the treatment of choice in patients with severe HS. This is best avoided until at least 6 years of age to reduce the risk of postsplenectomy sepsis.

  8. Health Library. Spherocytosis, Hereditary. Share. Print. What is Hereditary Spherocytosis? Spherocytosis, in most cases, is an inherited disease that changes the shape of and decreases the life of red blood cells. This destruction of the red blood cells leads to anemia. The shape of a normal red blood cell looks like a disk.