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Table 1 Median incidence of common chromosomal anomalies in omphalocele

From: Omphalocele: a review of common genetic etiologies

No.

% CA

Trisomy 18

Trisomy 13

Trisomy 21

Triploidy

TS

KS

Others

Authors

90

48.9 (44/90)

33

5

1

2

1

-

2

Brantberg et al., 2005 [9]

26

38 (10/26)

4

4

1

-

1

-

-

Nyberg et al., 1989 [25]

67

39 (26/67)

21

2

1

-

1

-

1

Fratelli et al., 2007 [26]

35

34 (12 /35)

10

2

0

-

-

-

-

Emer et al., 2015 [28]

35

54 (19/35)

17

-

-

1

-

1

-

Chen et al., 2007 [29]

18

67 (12/18)

10

1

-

1

-

-

-

Chen et al., 2007 [29]

271

(n = 123) 45.4

9577.2%

1411.4%

32.4%

43.25%

32.4%

10.8%

32.4%

 
  1. No., number of omphalocele; CA, chromosomal abnormalities; n, number of CA; S, syndrome; T, Turner; K, Klinefelter