HFE gene mutations in patients with altered iron metabolism in Argentina
Hereditary Hemochromatosis (HH) is an iron overload syndrome caused by increased duodenal iron absorption, which leads to excesive iron deposition in parenchymal cells of the liver and mayor organs, causing cirrhosis, diabetes, cardiac failure, endocrine complications and arthritis. There are 6 type...
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2009
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paper:paper_01455680_v55_n2_p31_Rossetti2023-06-08T15:12:28Z HFE gene mutations in patients with altered iron metabolism in Argentina Rossetti, María Victoria Mendez, Manuel Afonso, Susana Graciela Gerez, Esther Noemí Batlle, Alcira María del Carmen Parera, Victoria Estela Hereditary hemochromatosis HFE gene Iron metabolism Mutations iron Argentina article autosomal recessive inheritance female gene gene mutation hemochromatosis heterozygosity HFE gene human iron blood level iron metabolism major clinical study male prevalence Adolescent Adult Age of Onset Aged Argentina Child Female Gene Frequency Genotype Hemochromatosis Heterozygote Histocompatibility Antigens Class I Homozygote Humans Iron Male Membrane Proteins Middle Aged Polymorphism, Single Nucleotide Prevalence Young Adult Hereditary Hemochromatosis (HH) is an iron overload syndrome caused by increased duodenal iron absorption, which leads to excesive iron deposition in parenchymal cells of the liver and mayor organs, causing cirrhosis, diabetes, cardiac failure, endocrine complications and arthritis. There are 6 types of HH related to mutations in the genes that encode proteins of iron metabolism. HH Type I is inherited as an autosomal recessive trait of mutations in HFE gene. We investigate the prevalence of C282Y, H63D and S65C mutations in 95 individuals (77 males, 18 females) bearing iron metabolism alterations to establish an early diagnosis of HH. Among this population, 58% carried mutations in the HFE gene (45 males, 10 females). H63D mutation was found in 32.6% of the subjects (29.5% in heterozygocity, 3.15% in homozygocity). S65C mutation was only detected in the heterozygous form (5.3% of the patients), 2 of them carried also H63D mutation. C282Y in heterozygocity was found in 15.8% of the individuals; but only 4.15% carried this mutation in homozygocity. Our findings are in agreement with the prevalence of the Mediterranean origin of most of our patients, where C282Y mutation is not as common as H63D mutation. Copyright © 2009 C.M.B. Edition. Fil:Rossetti, M.V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Méndez, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Afonso, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Gerez, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Batlle, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Parera, V.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2009 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v55_n2_p31_Rossetti http://hdl.handle.net/20.500.12110/paper_01455680_v55_n2_p31_Rossetti |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
Hereditary hemochromatosis HFE gene Iron metabolism Mutations iron Argentina article autosomal recessive inheritance female gene gene mutation hemochromatosis heterozygosity HFE gene human iron blood level iron metabolism major clinical study male prevalence Adolescent Adult Age of Onset Aged Argentina Child Female Gene Frequency Genotype Hemochromatosis Heterozygote Histocompatibility Antigens Class I Homozygote Humans Iron Male Membrane Proteins Middle Aged Polymorphism, Single Nucleotide Prevalence Young Adult |
| spellingShingle |
Hereditary hemochromatosis HFE gene Iron metabolism Mutations iron Argentina article autosomal recessive inheritance female gene gene mutation hemochromatosis heterozygosity HFE gene human iron blood level iron metabolism major clinical study male prevalence Adolescent Adult Age of Onset Aged Argentina Child Female Gene Frequency Genotype Hemochromatosis Heterozygote Histocompatibility Antigens Class I Homozygote Humans Iron Male Membrane Proteins Middle Aged Polymorphism, Single Nucleotide Prevalence Young Adult Rossetti, María Victoria Mendez, Manuel Afonso, Susana Graciela Gerez, Esther Noemí Batlle, Alcira María del Carmen Parera, Victoria Estela HFE gene mutations in patients with altered iron metabolism in Argentina |
| topic_facet |
Hereditary hemochromatosis HFE gene Iron metabolism Mutations iron Argentina article autosomal recessive inheritance female gene gene mutation hemochromatosis heterozygosity HFE gene human iron blood level iron metabolism major clinical study male prevalence Adolescent Adult Age of Onset Aged Argentina Child Female Gene Frequency Genotype Hemochromatosis Heterozygote Histocompatibility Antigens Class I Homozygote Humans Iron Male Membrane Proteins Middle Aged Polymorphism, Single Nucleotide Prevalence Young Adult |
| description |
Hereditary Hemochromatosis (HH) is an iron overload syndrome caused by increased duodenal iron absorption, which leads to excesive iron deposition in parenchymal cells of the liver and mayor organs, causing cirrhosis, diabetes, cardiac failure, endocrine complications and arthritis. There are 6 types of HH related to mutations in the genes that encode proteins of iron metabolism. HH Type I is inherited as an autosomal recessive trait of mutations in HFE gene. We investigate the prevalence of C282Y, H63D and S65C mutations in 95 individuals (77 males, 18 females) bearing iron metabolism alterations to establish an early diagnosis of HH. Among this population, 58% carried mutations in the HFE gene (45 males, 10 females). H63D mutation was found in 32.6% of the subjects (29.5% in heterozygocity, 3.15% in homozygocity). S65C mutation was only detected in the heterozygous form (5.3% of the patients), 2 of them carried also H63D mutation. C282Y in heterozygocity was found in 15.8% of the individuals; but only 4.15% carried this mutation in homozygocity. Our findings are in agreement with the prevalence of the Mediterranean origin of most of our patients, where C282Y mutation is not as common as H63D mutation. Copyright © 2009 C.M.B. Edition. |
| author |
Rossetti, María Victoria Mendez, Manuel Afonso, Susana Graciela Gerez, Esther Noemí Batlle, Alcira María del Carmen Parera, Victoria Estela |
| author_facet |
Rossetti, María Victoria Mendez, Manuel Afonso, Susana Graciela Gerez, Esther Noemí Batlle, Alcira María del Carmen Parera, Victoria Estela |
| author_sort |
Rossetti, María Victoria |
| title |
HFE gene mutations in patients with altered iron metabolism in Argentina |
| title_short |
HFE gene mutations in patients with altered iron metabolism in Argentina |
| title_full |
HFE gene mutations in patients with altered iron metabolism in Argentina |
| title_fullStr |
HFE gene mutations in patients with altered iron metabolism in Argentina |
| title_full_unstemmed |
HFE gene mutations in patients with altered iron metabolism in Argentina |
| title_sort |
hfe gene mutations in patients with altered iron metabolism in argentina |
| publishDate |
2009 |
| url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v55_n2_p31_Rossetti http://hdl.handle.net/20.500.12110/paper_01455680_v55_n2_p31_Rossetti |
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