Background. The prevalence of beta -thalassemia in Mexico is not known in d
etail.
Methods. Data of studies investigating abnormal hemoglobins between Septemb
er 1987 and November 2000 were analyzed; in addition, data of red-blood-cel
l indices and clinical features were analyzed in patients identified as car
riers of beta -thalassemia.
Results. In 1,639 prospective studies looking for abnormal hemoglobins, 429
disclosed some abnormality; of these, 319 cases displayed abnormally high
levels of hemoglobin A2, thus consistent with the diagnosis of beta -thalas
semia. This hemoglobin abnormality represented 74.2% of all abnormalities,
both quantitative and qualitative, of the molecule of hemoglobin. There wer
e 317 heterozygotes and only two homozygotes. We have previously shown that
the most frequent cause of anemia as the iatrotropic condition in Mexican
mestizos is iron deficiency. We found that iron deficiency is 11.5 times mo
re frequent than beta -thalassemia and that the latter is 1.3 times more fr
equent than macrocytic/megaloblastic anemia.
Conclusions. beta -thalassemia should not be considered as infrequent in Me
xico, and individuals with red blood cell microcytosis and/or hypochromia w
ith or without anemia should be screened for thalassemia. (C) 2001 IMSS. Pu
blished by Elsevier Science Inc.