Treating iron overload in patients with non‐transfusion‐dependent thalassemia
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چکیده
منابع مشابه
Treating iron overload in patients with non-transfusion-dependent thalassemia
Despite receiving no or only occasional blood transfusions, patients with non-transfusion-dependent thalassemia (NTDT) have increased intestinal iron absorption and can accumulate iron to levels comparable with transfusion-dependent patients. This iron accumulation occurs more slowly in NTDT patients compared to transfusion-dependent thalassemia patients, and complications do not arise until la...
متن کاملEndocrine Dysfunctions in Iron Overload in Patients with Major Thalassemia
Abstract Background The aim of the present study was to determine the endocrine dysfunction in patients with major thalassemia, who receive hyper transfusion. Materials and Methods This cross sectional study was performed during one year, which included 65 major thalassemia patients (31 females and 34 males), aged between 14 month to 27 years old (median 10,3). Growth assessment was measur...
متن کاملendocrine dysfunctions in iron overload in patients with major thalassemia
abstract background the aim of the present study was to determine the endocrine dysfunction in patients with major thalassemia, who receive hyper transfusion. materials and methods this cross sectional study was performed during one year, which included 65 major thalassemia patients (31 females and 34 males), aged between 14 month to 27 years old (median 10,3). growth assessment was measured by...
متن کاملTreating thalassemia major-related iron overload: the role of deferiprone
Over the last 20 years, management for thalassemia major has improved to the point where we predict that patients' life expectancy will approach that of the normal population. These outcomes result from safer blood transfusions, the availability of three iron chelators, new imaging techniques that allow specific organ assessment of the degree of iron overload, and improvement in the treatment o...
متن کاملMyocardial iron overload in sickle/thalassemia patients of Italian origin
Background Sickle-thalassemia is an inherited hemoglobin disorder resulting from the combined heterozygosity for sicklecell and b-thalassemia genes. Myocardial iron overload in patients with sickle-thalassemia has been poorly studied; however, a report has shown no evidence of cardiac iron in a small group (n=10) of multitransfused Arab patients. The current study aims to further evaluate cardi...
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 2013
ISSN: 0361-8609,1096-8652
DOI: 10.1002/ajh.23405