exon deletion pattern in duchene muscular dystrophy in north west of iran

how to cite this article: barzegar m, habibi p, bonyady m, topchizadeh v, shiva sh. exon deletion pattern in duchene muscular dystrophy in north west of iran. iran j child neurol. 2015 winter; 9(1): 42-48. abstract objective duchene and becker muscular dystrophy (dmd/ bmd) are x-linked disorders that both are the result of heterogeneous mutations in the dystrophin gene. the frequency and distribution of dystrophin gene deletions in dmd/ bmd patients show different patterns among different populations. this study investigates the deletion rate, type, and distribution of this gene in the azeri turk population of north west iran. materials &methods; in this study, 110 patients with dmd/ bmd were studied for intragenic deletions in 24 exons and promoter regions of dystrophin genes by using multiplex pcr. results deletions were detected in 63 (57.3%) patients, and around 83% localized in the mid-distal hotspot of the gene (on exons 44–52), 21 cases (33.3 %) with singleexon deletions, and 42 cases (66.6%) with multi-exonic deletions. the most frequent deleted exons were exon 50 (15 %) and exon 49 (14%). no deletion was detected in exon 3. conclusion this study suggests that the frequency and pattern of dystrophin gene deletions in dmd/ bmd in the azeri turk population of north west iran occur in the same pattern when compared with other ethnic groups. references emery ae. clinical and molecular studies in duchenne muscular dystrophy. prog clin biol res 1989; 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