Mutations of the HFE gene among Turkish hereditary hemochromatosis patients

Simsek H., Balaban Y., Yilmaz E., Sumer H., Buyukasik Y., Cengiz C., ...Daha Fazla

ANNALS OF HEMATOLOGY, cilt.84, sa.10, ss.646-649, 2005 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 84 Konu: 10
  • Basım Tarihi: 2005
  • Doi Numarası: 10.1007/s00277-005-1048-y
  • Sayfa Sayıları: ss.646-649


Since the discovery of the HFE gene, C282Y and H63D mutations have been reported as significantly correlated with clinically manifested hereditary hemochromatosis (HH). As the other genes involved in iron metabolism have been described, non-HFE cases of HH have been identified. Since in the general Turkish population, the C282Y mutation is not found and the H63D mutation is of high frequency, we aimed to determine mutations in the HFE genes in our patients with HH. The HFE gene of the five patients with HH were sequenced. C282Y mutation was absent, and all HH patients were heterozygote for H63D mutation. No other mutation was found in HFE gene by sequencing. Although the higher allele frequency of the H63D mutation in Turkish HH patients than in the general population implies a role of the H63D mutation in iron overload, there is a strong possibility that Turkish HH patients have non-HFE hemochromatosis.