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2008 | 49 | 1 |

Tytuł artykułu

Frequency of mutations related to hereditary haemochromatosis in northwestern Poland

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Hereditary haemochromatosis has been linked with C282Y and H63D mutations of the HFE gene. In Europe, frequencies of these mutations are the highest in Northern European countries and gradually decrease southwards. We analysed the prevalence of HFE mutations in 1517 DNA samples, including 1000 samples from the general population (subjects registered at general practitioner practices) in northwestern Poland, and 517 samples of cord blood from the same region. We identified 2 (0.13%) homozygotes and 117 (7.8%) heterozygotes for the C282Y mutation. As regards the H63D mutation (1505 DNA samples analysed), 38 (2.5%) samples were homozygotes and 380 (25%) were heterozygotes. Twenty-one (1.4%) compound heterozygotes were found. These results correspond well with data from other Central European countries and seem to confirm the hypothesis of North-South spread of the C282Y mutation.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

49

Numer

1

Opis fizyczny

p.105-107,ref.

Twórcy

  • Liver Unit, Department of Gastroenterology, Pomeranian Medical University, Unii Lubelskiej 1, 71-252 Szczecin, Poland
autor
  • International Hereditary Cancer Centre, Department of Genetics and Pathology,Pomeranian Medical University, Szczecin, Poland
autor
  • International Hereditary Cancer Centre, Department of Genetics and Pathology,Pomeranian Medical University, Szczecin, Poland
autor
  • Liver Unit, Department of Gastroenterology, Pomeranian Medical University, Unii Lubelskiej 1, 71-252 Szczecin, Poland
autor
  • International Hereditary Cancer Centre, Department of Genetics and Pathology,Pomeranian Medical University, Szczecin, Poland
autor
  • Liver Unit, Department of Gastroenterology, Pomeranian Medical University, Unii Lubelskiej 1, 71-252 Szczecin, Poland

Bibliografia

  • ArandaN, Viteri FE, Fernandez-Ballart J, Murphy M, Arija V, 2007. Frequency of the hemochromatosis gene (HFE) 282C-->Y, 63H-->D, and 65S-->C mutations in a general Mediterranean population from Tarragona, Spain. Ann Hematol 86: 17-21.
  • Campbell S, George DK, Robb SD, Spooner R, McDonagh TA, Dargie HJ, Mills PR, 2003. The prevalence of haemochromatosis gene mutations in the West of Scotland and their relation to ischaemic heart disease. Heart 89: 1023-1026.
  • Cimburova M, Putova I, Provazníkova H, Pinterova D, Horak J, 2005. S65C and other mutations in the haemochromatosis gene in the Czech population. Folia Biol (Praha) 51: 172-176.
  • Distante S, Berg JP, Lande K, Haug E, Bell H, 1999. High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression. Scand J Gastroenterol 34: 529-534.
  • Floreani A, Rizzotto ER, Basso D, Navaglia F, Zaninotto M, Petridis I, et al. 2007. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy. Aliment Pharmacol Ther 26: 577-586.
  • Jezequel P, Bargain M, Lellouche F, Geffroy F, Dorval I, 1998. Allele frequencies of hereditary hemochromatosis gene mutations in a local population of west Brittany. Hum Genet 102: 332-333.
  • Meier P, Schuff-Werner P, Steiner M, 2005. Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany. Clin Lab 51: 539-543.
  • Milman N, Pedersen P, Ovesen L, Melsen GV, Fenger K, 2004. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in 2501 ethnic Danes. Ann Hematol 83: 654-657.
  • Moczulski DK, Grzeszczak W, Gawlik B, 2001. Frequency of the hemochromatosis C282Y and H63D mutations in a Polish population of Slavic origin. Med Sci Monit 7: 441-443.
  • Potekhina ES, Lavrov AV, Samokhodskaya LM, Efimenko AY, Balatskiy AV, Baev AA, et al. 2005. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients. Blood Cells Mol Dis 35: 182-188.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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