Hyperferritinaemia in the absence of iron overload

Background—Serum ferritin is normally a marker of iron overload. Ferritin genes are sited at chromosomes 19 and 11. Regulation of ferritin synthesis involves an interaction between an iron regulatory protein (IRP) and part of the ferritin mRNA designated the iron regulatory element (IRE). A disorder...

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Veröffentlicht in:	Gut 1997-09, Vol.41 (3), p.408-410
Hauptverfasser:	Arnold, J D, Mumford, A D, Lindsay, J O, Hegde, U, Hagan, M, Hawkins, J R
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Case Report cataract Cataract - blood Cataract - genetics Cataracts Chromosomes, Human, Pair 19 Deoxyribonucleic acid DNA Errors of metabolism Female ferritin Ferritins - blood Ferritins - genetics Gastroenterology Genes Genes, Dominant Genetic testing hereditary haemochromatosis Humans hyperferritinaemia In Situ Hybridization Iron - blood Iron Metabolism Disorders - blood Iron Metabolism Disorders - genetics iron overload Medical sciences Metabolic diseases Mutation Pedigree Point Mutation Polymerase Chain Reaction Proteins Proteins and glycoproteins Transferrin - metabolism
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