Análisis de los polimorfismos G199A, Ncol del gen ANK1 y Memphis I del gen SLC4A1 en Individuos sanos y pacientes mexicanos con esferocitosis hereditaria

background. in mexico, hereditary spherocytosis (hs) is the main cause of hereditary hemolytic anemia, due to mutations of one or more genes involved in the erythrocyte membrane, making it difficult to identify the primary gene. objective. with the purpose of estimating the use of the polymorphisms g199a and ncol of ankl gene, and memphis i of slc4a1 gene, as genetic markers to screen this disease, we searched the allelic and genotypic frequencies in 45 dna samples of hs patients and 28 from healthy individuals. results. allelic and genotypic frequencies were similar in both studied groups for the g199a and memphis i polymorphisms, with low frequency of heterozygosis showing its limited use as a genetic marker. the allelic and genotypic frequencies of the ncol polymorphism were also similar in both groups, however a higher heterozygote frequency was observed (0.49 and 0.43 in patients and healthy individuals), a feature that may turn it into a useful genetic marker. conclusions. since there are other genes implicated in the molecular pathology of the hs, we consider it necessary to continue analyzing other polymorphisms of the genes involved in hereditary spherocytosis among the mexican population,