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Table 3 The frequency of chromatid and chromosome breaks in young mothers with DS children and control mothers

From: The demographic data and the high frequency of chromosome/chromatid breaks as biomarkers for genome integrity have a role in predicting the susceptibility to have Down syndrome in a cohort of Egyptian young-aged mothers

Cytogenetic defect

DS mothers

Control mothers

OR (95% CI)

P value

Chromatid breaks

    

 Frequency

34/50 (68%)

10/50 (20%)

8.50 (3.411–21.17)

< 0.001*

 Mean ± SD

3.68 ± 2.54

1.29 ± 0.84

  

Chromosome breaks

    

 Frequency

18/50 (36%)

6/50 (12%)

3.93 (1.40–11.05)

0.009*

 Mean ± SD

2.45 ± 3.32

0.86 ± 0.69

  
  1. *Statistically significant at P ≤ 0.05