Please use this identifier to cite or link to this item:
Title: Types and frequencies of hemoglobin disorders in the pacific coast of four states of Mexico
Author: Cobian, J.G.
Sanchez-Lopez, J.Y.
Magana, M.T.
Chavez, M.L.
Perea, F.J.
Ibarra, B.
Issue Date: 2009
Abstract: Introduction. Hemoglobin disorders are classified into three main groups: structural variants, thalassemias (thal) and hereditary persistence of fetal hemoglobin (HPFH). Objective. This study describes the types and frequencies of hemoglobinopathies from four states of the Pacific coast of Mexico (Jalisco, Colima, Nayarit and Michoacan). Material and methods. We studied 1513 Mexican individuals by hematological and biochemical analysis following the conventional methods, DNA analysis was carried out in abnormal samples. Results. The frequency of hemoglobinopathies was 1.258%. Structural variants were the most common type (0.726%), with seven carriers (0.462%) and one homozygote (0.066%) for Hb S, and three heterozygotes of the following hemoglobins: C (?6 Glu-?Lys), Fannin-Lubbock I (?119 Gly-?Asp) and Colima (?49 Ser-?Cys), with a frequency of 0.066% each. We observed a frequency of 0.466% for the thalassemia group, with one homozygote for the ?3.7 (-thal) allele (0.066%), and 6 heterozygotes for ?-thal (0.40%), with the allele IVS1:110 G-?A in three subjects, and the alleles Cd 39, IVS1:5 G-?A and -28 A-?C in the three other. HPFH was detected in one subject (0.066%). Jalisco and Colima had the highest frequencies of hemoglobinopathies, 3.015% and 1.331% respectively, and the latter showed the most diversity of hemoglobin disorders. Conclusions. The observed heterogeneity of types and frequencies of hemoglobinopathies in the regions studied illustrate the importance of further investigation of these abnormalities in Mexico.
Appears in Collections:Producción científica UdeG

Files in This Item:
There are no files associated with this item.

Items in RIUdeG are protected by copyright, with all rights reserved, unless otherwise indicated.