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Table 5 Genotype distribution of MTHFR in DSM and neonatal jaundice in the DS child

From: MTHFR gene polymorphism and associated nutritional deficiency in the etiology and pathogenesis of Down syndrome

Genotype DSM group
No neonatal jaundice
n, f(%)
Neonatal jaundice
n, f(%)
OR (CI) p value
CC 31 (26.2) 11 (9.3) Reference Reference
CT 45 (38.1) 31 (26.2) 1.9 (0.8 to 4.4) p = 0.1128NS
  1. n number of genotype, f frequency, OR odds ratio, CI 95% confidence interval, NS not significant