Hereditary spherocytosis medical therapy: Difference between revisions

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Revision as of 21:01, 20 February 2018

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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 ==Overview==
 ==Medical Therapy==
-As in [[spherocytosis|non-hereditary spherocytosis]], acute symptoms of [[anemia]] and hyperbilirubinemia indicate treatment with [[blood transfusion]]s 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.
 ==References==
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 {{WH}}
 {{WS}}
 [[Category:Hematology]]
 [[Category:Pediatrics]]