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May 19, 2022 · Hereditary spherocytosis is an inherited blood disorder that causes hemolytic anemia. Learn about the symptoms, causes and how doctors diagnose this condition with blood tests and other methods.
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What is the differential diagnosis for hereditary spherocytosis?
What is hereditary spherocytosis?
What tests are required to diagnose hereditary spherocytosis (HS)?
Jul 4, 2023 · The differential diagnosis for patients with hereditary spherocytosis is broad and includes other red blood cell disorders including elliptocytosis and its variants, hereditary stomatocytosis, pyropoikilocytosis, and ovalocytosis.
- Edgar A. Zamora, Catherine A. Schaefer
- 2023/07/04
Oct 25, 2023 · Learn about the causes, symptoms, and diagnosis of hereditary spherocytosis (HS), the most common inherited red cell membrane defect. HS is caused by mutations in five genes that affect RBC membrane proteins and cytoskeleton.
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...
Diagnosis of Spherocytosis. Doctors have several ways to test for spherocytosis, such as blood tests and checking the spleen. Due to the hereditary nature of spherocytosis, parents with a family history should have their children tested. Some babies with hereditary spherocytosis can have jaundice, often at birth.
Oct 24, 2021 · Hereditary spherocytosis (HS) is a hereditary hemolytic anemia caused by the mutations in the genes encoding erythrocyte membrane proteins and is mostly inherited in an autosomal dominant manner. 1, 2, 3 HS is classified into four types according to the severity of the disease: trait, mild, moderate, and severe. Commonly, there is heterogeneity ...
Jun 20, 2023 · Learn about the symptoms, diagnosis and treatment of hereditary spherocytosis, an inherited abnormality of the red blood cell that causes haemolytic anaemia. Find out how to perform blood tests, genetic analysis, and splenectomy for patients with different severity of the disorder.
