[No authors listed]
BACKGROUND:Hirschsprung disease (HSCR, aganglionic megacolon) is the most frequent genetic cause of congenital intestinal obstruction. DSCAM was identified as associated to HSCR with Down Syndrome (DS-HSCR) in European population,but failed to replicate in the non-syndromic HSCR patients. We aim to further investigate the relationship of DSCAM with non-sydromic HSCR in a South Chinese cohort, the largest case-control study so far. METHOD:We analyzed 1394 HSCR patients and 973 healthy controls. Two polymorphisms (rs2837770 Aâ>âG, rs8134673 Aâ>âG) on DSCAM were genotyped using Sequenom Massarray platform. RESULTS:Both SNPs were confirmed as associated with non-syndromic HSCR in the South Chinese population (Pâ=â1.69E-03, ORâ=â1.29 for SNP rs2837770 and Pâ=â3.00E-03, ORâ=â1.27 for SNP rs8134637). Of note, we demonstrated the associated SNPs were more likely to affect a subgroup of patients with short-segment aganglionosis (S-HSCR) (Pâ=â3.06E-03,ORâ=â1.21 for SNP rs2837770 and Pâ=â3.33E-03,ORâ=â1.21 for SNP rs8134637). CONCLUSION:There is an association between DSCAM polymorphisms and non-syndromic HSCR in South Chinese population.
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