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. 2021 Mar 18;16(3):e0248894. doi: 10.1371/journal.pone.0248894

Table 5. Prevalence of extracardiac anomalies by type of congenital heart disease (live birth only).

No Type N ECM a Chromosomal anomaly b 22q11.2 microdeletion b ECA c
1 Heterotaxy, including isomerism and mirror-imagery 19 8 (42.1) 0/12 (0) 0/7 (0) 8 (42.1)
2 Anomalies of the venous return 14 3 (21.4) 0/3 (0) 0/0 3 (21.4)
3 Anomalies of the atria and interatrial communications 25 6 (24.0) 2/8 (25.0) 0/3 (0) 8 (32.0)
4 Anomalies of the atrioventricular junctions and valves 37 10 (27.0) 4/17 (23.5) 0/5 (0) 12 (32.4)
5 Complex anomalies of atrioventricular connections 5 0 (0) 0/2 (0) 0/0 0 (0)
6 Functionally univentricular hearts 31 5 (16.1) 2/17 (11.8) 0/12 (0) 5 (16.1)
7 Ventricular septal defects 47 12 (25.5) 3/21 (14.3) 0/7 (0) 14 (29.8)
8 Anomalies of the ventricular outflow tracts 169 43 (25.4) 10/107 (9.3) 3/76 (3.9) 50 (29.6)
9 Anomalies of the extrapericardial arterial trunks 63 17 (27.0) 1/30 (3.3) 3/19 (15.8) 17 (27.0)
10 Other unclassified anomalies 10 4 (40.0) 0/2 (0) 0/0 4 (40.0)
Total 420 108 (25.7) 22/219 (10.0) 6/129 (4.7) 121 (28.8)

Data are shown in number (%).

ECM, extracardiac malformations; ECA, extracardiac anomalies.

a extracardiac malformations, defined as extracardiac structural malformation.

b denominators were those who underwent the examination during either prenatal or postnatal periods.

c extracardiac anomalies, defined as having any ECM or chromosomal anomaly or 22q11.2 microdeletion.