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Journal ArticleDOI

Mutation Analysis in Hereditary Hemochromatosis

TLDR
The DNA of 147 patients of European origin clinically diagnosed with idiopathic hemochromatosis and 193 controls was examined for mutations of the HLA-H gene at nt 845 and nt 187, suggesting the presence of as yet undiscovered mutations existing in trans with 845A and in linkage disequilibrium with 187G.
Abstract
The DNA of 147 patients of European origin clinically diagnosed with idiopathic hemochromatosis and 193 controls was examined for mutations of the HLA-H gene at nt 845 and nt 187. One hundred twenty-one (82.3%) of the hemochromatosis patients were homozygous and 10 (6.8%) heterozygous for the 845A (C282Y) mutation. All of the homozygous patients were also homozygous for nt 187C, and all 845A heterozygotes had at least one copy of 187C. Thus, the nt 845 and nt 187 mutations were in complete linkage disequilibrium; nt 187 was a C on all chromosomes with the 845A mutation. Eight of the 10 heterozygotes for 845A were heterozygous for 187G(H63D). The excess of heterozygotes at both nt 187 and nt 845 suggested either the presence of as yet undiscovered mutations existing in trans with 845A and in linkage disequilibrium with 187G, or that the 187G itself is a deleterious mutation, which in concert with the 845A can give rise to hemochromatosis. None of the 193 normal controls were homozygous for 845A and 29/193 (15%) were heterozygous for 845A. Although 47/193 (24.3%) of normal controls were heterozygous for the 187G mutation only two of these carried the 845A mutation. If the 187G mutation complemented the 845A mutation with high penetrance in causing hemochromatosis, then the population frequency of the two genes would require that a high proportion of patients with hemochromatosis be heterozygous for 845A and 187G. Instead, the frequency of homozygotes for the 845A mutation was much higher than that of the 845A/187G genotype. Based on our data, the penetrance of the 845A/187G genotype is only 1.5% and based on the data of Feder et al. only 0.5%. In contrast, the penetrance of the homozygous 845A/845A genotype seems to be very high. Thus, screening for this genotype should be very useful.

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Citations
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Journal ArticleDOI

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22

TL;DR: A homozygous nonsense mutation in the gene encoding transferrin receptor-2 (TFR2) is found in people with haemochromatosis that maps to HFE3 and a new locus (HFE3) is reported on 7q22.
Journal ArticleDOI

Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

TL;DR: The normal age distribution of people with the haemochromatosis genotype, and the lack of symptoms in patients of all ages, indicate that the penetrance of hereditary haemosynthesis is much lower than generally thought.
Journal ArticleDOI

Global prevalence of putative haemochromatosis mutations.

TL;DR: The distribution of the C282Y mutation coincides with that of populations in which haemochromatosis has been reported and is consistent with the theory of a north European origin for the mutation.
Journal ArticleDOI

A Population-Based Study of the Clinical Expression of the Hemochromatosis Gene

TL;DR: Eight of the 16 homozygous subjects had clinical findings that were consistent with the presence of hereditary hemochromatosis, such as hepatomegaly, skin pigmentation, and arthritis, in a population of white adults of northern European ancestry.
Journal ArticleDOI

Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis

TL;DR: The Cys282Tyr mutation is responsible for most of the mild iron overload found in NASH and thus has a significant association with hepatic damage in these patients, which cannot always be considered benign.
References
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Journal Article

A novel MHC class-I-like gene is mutated in patients with hereditary haemochromatosis

John N. Feder
- 01 Jan 1996 - 
TL;DR: Using linkage–disequilibrium and full haplotype analysis, a region more than 3 megabases telomeric of the major histocompatibility complex (MHC) that is identical–by–descent in 85% of patient chromosomes is identified, containing a gene related to the MHC class I family, termed HLA–H, containing two missense alterations.
Journal ArticleDOI

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

TL;DR: The value of population screening is demonstrated in these studies by the detection of homozygotes before clinical manifestations of hemochromatosis occur, and the efficacy of transferrin saturation as a screening tool for hemochROMatosis is determined.
Journal ArticleDOI

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis.

M. Simon, +3 more
- 01 May 1976 - 
TL;DR: This finding strongly supports the suggestion that idiopathic haemochromatosis is a genetic disease and suggests that the gene(s) responsible for the disease may be linked to the histocompatibility genes.
Journal ArticleDOI

beta2 knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism

TL;DR: Results indicate beta2m-associated proteins are involved in the control of intestinal Fe absorption, and predicted that mice which have altered expression of class I gene products, the beta2-microglobulin knockout mice, would develop Fe overload, were confirmed.
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