Hereditary spherocytosis medical therapy: Difference between revisions
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Revision as of 19:13, 23 June 2016
Hereditary spherocytosis Microchapters |
Differentiating Hereditary spherocytosis from other Diseases |
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Hereditary spherocytosis medical therapy On the Web |
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Risk calculators and risk factors for Hereditary spherocytosis medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Medical Therapy
As in non-hereditary spherocytosis, acute symptoms of anemia and hyperbilirubinemia indicate treatment with blood transfusions or exchanges and chronic symptoms of anemia and splenomegaly indicate dietary supplementation of iron and splenectomy, the surgical removal of the spleen.
Experimental gene therapy exists to treat hereditary spherocytosis in lab mice; however, this treatment has not yet been tried on humans and because of the risks involved in human gene therapy, it may never be.