Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2002-3-11
pubmed:abstractText
The hemochromatosis gene, HFE, is located on chromosome 6 in close proximity to the HLA-A locus. Most Caucasian patients with hereditary hemochromatosis (HH) are homozygous for HLA-A3 and for the C282Y mutation of the HFE gene, while a minority are compound heterozygotes for C282Y and H63D. The prevalence of these mutations in non-Caucasian patients with HH is lower than expected. The objective of the present study was to evaluate the frequencies of HLA-A antigens and the C282Y and H63D mutations of the HFE gene in Brazilian patients with HH and to compare clinical and laboratory profiles of C282Y-positive and -negative patients with HH. The frequencies of HLA-A and C282Y and H63D mutations were determined by PCR-based methods in 15 male patients (median age 44 (20-72) years) with HH. Eight patients (53%) were homozygous and one (7%) was heterozygous for the C282Y mutation. None had compound heterozygosity for C282Y and H63D mutations. All but three C282Y homozygotes were positive for HLA-A3 and three other patients without C282Y were shown to be either heterozygous (N = 2) or homozygous (N = 1) for HLA-A3. Patients homozygous for the C282Y mutation had higher ferritin levels and lower age at onset, but the difference was not significant. The presence of C282Y homozygosity in roughly half of the Brazilian patients with HH, together with the findings of HLA-A homozygosity in C282Y-negative subjects, suggest that other mutations in the HFE gene or in other genes involved in iron homeostasis might also be linked to HH in Brazil.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0100-879X
pubmed:author
pubmed:issnType
Print
pubmed:volume
35
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
329-35
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11887210-Adult, pubmed-meshheading:11887210-Age of Onset, pubmed-meshheading:11887210-Aged, pubmed-meshheading:11887210-Amino Acid Substitution, pubmed-meshheading:11887210-Base Sequence, pubmed-meshheading:11887210-Brazil, pubmed-meshheading:11887210-Genetic Testing, pubmed-meshheading:11887210-HLA Antigens, pubmed-meshheading:11887210-HLA-A Antigens, pubmed-meshheading:11887210-Hemochromatosis, pubmed-meshheading:11887210-Heterozygote, pubmed-meshheading:11887210-Histocompatibility Antigens Class I, pubmed-meshheading:11887210-Homozygote, pubmed-meshheading:11887210-Humans, pubmed-meshheading:11887210-Male, pubmed-meshheading:11887210-Membrane Proteins, pubmed-meshheading:11887210-Middle Aged, pubmed-meshheading:11887210-Mutation, pubmed-meshheading:11887210-Prevalence
pubmed:year
2002
pubmed:articleTitle
Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
pubmed:affiliation
Hospital Português de Salvador, Salvador, BA, Brasil. plbbr@uol.com.br
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't