Yahoo Web Search

Search results

  1. May 19, 2022 · Hereditary spherocytosis is a rare inherited disorder that requires lifelong medical care. Healthcare providers can treat the sometimes-serious medical conditions that hereditary spherocytosis causes. They cant cure the blood disorder, though. It’s not always easy to have a chronic illness or care for someone who does.

  2. Feb 14, 2024 · Hereditary spherocytosis is a disorder in which the red blood cells are abnormal and fragile. Learn about the causes, symptoms, and treatment options for this disorder today.

  3. 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...

  4. 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. Symptoms, generally milder in hereditary elliptocytosis, include variable degrees of anemia, jaundice, and splenomegaly.

  5. Mar 15, 2023 · The treatment for hereditary spherocytosis is individualized and may require transfusions, folic acid administration, full or partial splenectomy, and/or cholecystectomy. Complications of spherocytosis may include megaloblastic crisis, low folic acid levels, splenomegaly, and/or gallbladder problems.

  6. Aug 5, 2019 · Suspicion for HS is based on clinical features and a family history of spherocytosis or related symptoms. Diagnosis is confirmed based on blood tests. Surgical removal of the spleen (splenectomy) is used as a cure for HS in the case of severe anemia. Other treatments include extra folate (folate supplementation) and blood transfusions.

  7. People also ask

  8. Mar 22, 2023 · Splenectomy is the definitive treatment for HS. Except in the unusual autosomal recessive variant of HS, splenectomy usually eliminates hemolysis and the associated signs and symptoms.

  1. People also search for