2018
DOI: 10.1136/bcr-2017-222700
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Inherited haemochromatosis with C282Y mutation in a patient with alpha-thalassaemia: a treatment dilemma

Abstract: A Caucasian 24-year-old female patient suffers from two hereditary disorders: alpha-thalassaemia, which is prevalent in Asia and rare in Europe, and haemochromatosis, which is prevalent among northern Europe and rare in Asia. The clinical presentation and management of one of these diseases is controversial for the other. She presented 5 years ago with a clinical picture of refractory iron-deficiency anaemia secondary to menorrhagia. On treating her with the standard iron therapy, her anaemia persists although… Show more

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