A case of hypophosphataemic osteomalacia secondary to deferasirox therapy

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Abstract

Patients with beta-thalassemia major require iron-chelation therapy to avoid the complication of iron overload. Until recently, deferoxamine (DFO) was the major iron chelator used in patients requiring chronic hypertransfusion therapy, but DFO required continuous subcutaneous therapy. The availability of deferasirox (Exjade(R)), an orally active iron chelator, over the past 4 years represented a necessary alternative for patients requiring chelation therapy. However, there have been increasing reports of proximal renal tubular dysfunction and Fanconi Syndrome associated with deferasirox in the literature. We report a case of hypophosphataemic osteomalacia secondary to deferasirox therapy. (c) 2012 American Society for Bone and Mineral Research.
Original languageEnglish
Pages (from-to)219 - 222
Number of pages4
JournalJournal of Bone and Mineral Research
Volume27
Issue number1
DOIs
Publication statusPublished - 2012

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