New England Journal of Medicine · 1979 · 300 citations · 8 references
MedicineGeneticsHematologyHuman GeneticsIron Metabolism DisordersMedical GeneticsAnemiaClinical HematologyGenetic DisordersHereditary HemochromatosisLiver DiseaseEarly DiagnosisEarly Disease DetectionEarly Disease ScreeningHepatic Iron AccumulationHepatic Iron Overload AssessmentHepatic Iron StorageHereditary Hemochromatosis TreatmentTransferrin Deficiency
Previous studies have shown that hemochromatosis is an inherited, autosomal-recessive disease and that the gene is closely linked to the HLA locus on chromosome 6. We obtained a lod score for linkage of +9.8 for a recombination fraction of 0.0 and a gene frequency of 0.056, the frequency estimated in this population. We studied the phenotypic expression of the disease in 261 members of 10 pedigrees. In heterozygotes over 20 years of age, there was an intermediate increase in transferrin saturation and a limited increase in hepatic iron but no clinical manifestations. In male heterozygotes, the average amount of iron in the liver increased from about 0.2 to 1.3 g. Abnormal homozygotes accumulated iron progressively with time, with men accumulating about 18 g in the liver. All measurements of iron status were increased in abnormal homozygotes. Hemochromatosis is inherited as an autosomal-recessive disease, with partial biochemical expression in heterozygotes.
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IDIOPATHIC HEMOCHROMATOSIS, AN IRON STORAGE DISEASE
Stuart C. Finch, Clement A. Finch · Medicine · 1955 · 582 citations
M. K. Simon, M Bourel, B Genetet et al. · New England Journal of Medicine · 1977 · 362 citations
Medicine, Hematology, Pathology +11
Corwin Q. Edwards, Michael P. Carroll, Paul Bray et al. · New England Journal of Medicine · 1977 · 141 citations
Medicine, Genetics, Hematology +16