What is hereditary spherocytosis diseases

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A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Hereditary spherocytosis. I was 37 when I was diagnosed. I had my spleen and gallbladder removed. The last two years I find myself getting really tired and fall asleep for a few minutes to . 6 days ago Hereditary spherocytosis is a condition that affects red blood cells. People with this condition Genetic and Rare Diseases Information Center.

Hereditary spherocytosis (HS) is a familial hemolytic disorder associated anemia (ie, HS), long periods of asymptomatic disease depend on a. Hereditary spherocytosis can range from mild to severe. Symptoms vary depending on the severity of the disease. Most individuals with HS. Hereditary spherocytosis makes the outer shell of red blood cells very fragile. Children's, we offer a full range of services to diagnose and treat this disease.

Hereditary spherocytosis (HS) is an inherited blood disease that results in anemia. If your child has HS, either parent may also have the disease; however. Clotting Disorders Overview · Blood Clot Formation (Thrombosis) · Inherited Causes of Disorders» Other Hematological Disorders» Hereditary Spherocytosis. Symptoms of the following disorders can be similar to those of Hereditary Hemolytic Spherocytic Anemia. Comparisons may. Hereditary spherocytosis is a conditions that is treated in the If there is no family history and the disease is mild, the diagnosis of HS may be delayed into.