2009, Number 5
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Rev Invest Clin 2009; 61 (5)
Types and frequencies of hemoglobin disorders in the pacific coast of four states of Mexico
Cobián JG, Sánchez-López JY, Magaña MT, Chávez ML, Perea FJ, Ibarra B
Language: English
References: 39
Page: 399-404
PDF size: 73.10 Kb.
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 (β6
Glu→Lys), Fannin-Lubbock I (β119 Gly→Asp) and Colima
(β49 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 α
3.7 (-thal) allele (0.066%), and 6 heterozygotes
for β-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.
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