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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Detalles Bibliográficos
Autores principales: Rossetti, M.V., Méndez, M., Afonso, S., Gerez, E., Batlle, A., Muñoz, A., Parera, V.E.
Formato: JOUR
Materias:
Hereditary hemochromatosis
HFE gene
Iron metabolism
Mutations
iron
Argentina
article
autosomal recessive inheritance
female
gene
gene mutation
hemochromatosis
heterozygosity
human
iron blood level
iron metabolism
major clinical study
male
prevalence
Adolescent
Adult
Age of Onset
Aged
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
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_01455680_v55_n2_p31_Rossetti
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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