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Table 3 Detection rates of chromosomal abnormalities in fetuses with CHD plus additional structural anomalies

From: Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study

CHD with additional structural anomalies

n

Chromosomal abnormalities

Total

Aneuploidy

pCNV

CHD with single additional structural anomaly

36

12

6

6

Central nervous system

3

2

1

1

Gastrointestinal system

2

1

1

0

Urinary tract system

4

1

0

1

Respiratory system

2

0

0

0

Skeletal system

10

4

3

1

Face

8

3

1

2

Cystic hygroma

6

1

0

1

Abdominal wall

1

0

0

0

CHD with multiple additional structural anomalies

8

3

2

1

  1. Bold indicates a major category