PubMed:10942934
Annnotations
{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/10942934","sourcedb":"PubMed","sourceid":"10942934","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/10942934","text":"Juvenile hemochromatosis associated with B-thalassemia treated by phlebotomy and recombinant human erythropoietin.\nJuvenile hemochromatosis is a rare genetic disorder that causes iron overload. Clinical complications, which include liver cirrhosis, heart failure, hypogonadotropic hypogonadism and diabetes, appear earlier and are more severe than in HFE-related hemochromatosis. This disorder, therefore, requires an aggressive therapeutic approach to achieve iron depletion. We report here the case of a young Italian female with juvenile hemochromatosis who was unable to tolerate frequent phlebotomy because of coexistent ss-thalassemia trait. The patient was successfully iron-depleted by combining phlebotomy with recombinant human 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