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Revista Romana de PEDIATRIE | Volumul LX, Nr. 4, An 2011
ISSN 1454-0398  |  e-ISSN 2069-6175
ISSN-L 1454-0398
DOI: 10.37897/RJP

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Hemochromatosis assesment in β thalassaemia major

and

ABSTRACT

β thalassaemia major is a severe anaemia which requires lifetime transfusional treatment, without it the patient would not survive. The chronic transfusional regimen causes an iron overload which needs a regular monitoring for establishing an effective iron chelation therapy.

Key words: β thalassaemia major, iron overload

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