Inherited haemochromatosis with C282Y mutation in a patient with alpha-thalassaemia: a treatment dilemma
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DOI: 10.1136/bcr-2017-222700
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… read more here.
Keywords: alpha thalassaemia; treatment; iron; haemochromatosis ... See more keywords
A Review of Nutrients and Compounds, Which Promote or Inhibit Intestinal Iron Absorption: Making a Platform for Dietary Measures That Can Reduce Iron Uptake in Patients with Genetic Haemochromatosis
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DOI: 10.1155/2020/7373498
Abstract: Objective To provide an overview of nutrients and compounds, which influence human intestinal iron absorption, thereby making a platform for elaboration of dietary recommendations that can reduce iron uptake in patients with genetic haemochromatosis. Design… read more here.
Keywords: iron uptake; reduce iron; haemochromatosis; iron ... See more keywords