Details

Autor(en) / Beteiligte

• Leão, Gioconda Dias Rodrigues
• Freire, Juliana Mendonça
• Cunha Fernandes, Andrea Luciana Araújo
• Moura de Oliveira, Taissa Maria
• Leão, Nilma Dias
• Gil, Erica Aires
• de Vasconcelos, Roberto Chaves
• Azevedo, João Paulo da Silva
• de Farias Sales, Valéria Soraya
• de Araújo Moura Lemos, Telma Maria
• Leão, Marcos Dias
• do Nascimento Jr, Francisco Fernandes
• Maciel, James Farley Rafael
• de Freitas, Rodrigo Villar
• de Souza Paiva, Aldair
• Cavalcanti Jr, Geraldo Barroso

Titel

Analysis of HFE Genes C282Y, H63D, and S65D in Patients With Hyperferritinemia From Northeastern Brazil

Ist Teil von

• Journal of clinical laboratory analysis, 2014-05, Vol.28 (3), p.178-185

Ort / Verlag

United States: Blackwell Publishing Ltd

Erscheinungsjahr

2014

Link zum Volltext

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• Background Hereditary hemochromatosis (HH) is a genetic disease caused by the high absorption and deposition of iron in several organs. This accumulation results in several clinical complications such as cirrhosis, arthritis, cardiopathies, diabetes, sexual disorders, and skin darkening. The H63D and C282Y mutations are well defined in the HH etiology. The objective of this article is identification of the H63D and C282Y mutations in the HFE protein gene and the frequency assessment of these mutations in patients with persistent increase of serum ferritin in patients from Natal City from state of Rio Grande do Norte, located in northeastern Brazil. Results Of the 299 patients studied for C282Y and H63D, 48.49% showed absence of mutation and 51.51% showed some sort of mutation: heterozygous C282Y mutation in 4.35% patients, homozygous C282Y mutation in 2.67% patients, heterozygous H63D mutation in 31.44% patients, homozygous H63D mutation in 8.03% patients, and heterozygous for the mutation in both genes (C282Y/H63D) in 5.02% patients. The S65C mutation was studied in 112 patients and heterozygous mutation (S65D/WT) in 2.67% of patients and double mutation (H63D/S65C) in 1.78% of patients were observed. Conclusion Due to the high prevalence of hemochromatosis, its genetic diagnosis has become a challenge, especially in the high‐risk group.