Table 1
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Incidence of associated anomalies in neonates with esophageal atresia

AnomalyNumber of cases (%)
Congenital heart disease35 (39.8%)
Ventricular septal defect15 (17%)
Atrial septal defect12 (13.6%)
Musculoskeletal23 (26.1%)
Vertebral abnormality13 (14.8%)
Limb abnormality9 (10.2%)
Genitourinary26 (25%)
Renal abnormality21 (23.9%)
Genital/urinary abnormality5 (1.1%)
Intestinal7 (8%)
Imperforate anus5 (5.7%)
Atresia2 (2.3)
Intracranial/cranial facial9 (10.2%)
Craniofacial abnormality5 (5.7%)
Chromosomal8 (9.1%)
Trisomy 212 (2.3%)
VACTERL association11 (12.5%)
AnomalyNumber of cases (%)
Congenital heart disease35 (39.8%)
Ventricular septal defect15 (17%)
Atrial septal defect12 (13.6%)
Musculoskeletal23 (26.1%)
Vertebral abnormality13 (14.8%)
Limb abnormality9 (10.2%)
Genitourinary26 (25%)
Renal abnormality21 (23.9%)
Genital/urinary abnormality5 (1.1%)
Intestinal7 (8%)
Imperforate anus5 (5.7%)
Atresia2 (2.3)
Intracranial/cranial facial9 (10.2%)
Craniofacial abnormality5 (5.7%)
Chromosomal8 (9.1%)
Trisomy 212 (2.3%)
VACTERL association11 (12.5%)
Table 1
Open in new tab

Incidence of associated anomalies in neonates with esophageal atresia

AnomalyNumber of cases (%)
Congenital heart disease35 (39.8%)
Ventricular septal defect15 (17%)
Atrial septal defect12 (13.6%)
Musculoskeletal23 (26.1%)
Vertebral abnormality13 (14.8%)
Limb abnormality9 (10.2%)
Genitourinary26 (25%)
Renal abnormality21 (23.9%)
Genital/urinary abnormality5 (1.1%)
Intestinal7 (8%)
Imperforate anus5 (5.7%)
Atresia2 (2.3)
Intracranial/cranial facial9 (10.2%)
Craniofacial abnormality5 (5.7%)
Chromosomal8 (9.1%)
Trisomy 212 (2.3%)
VACTERL association11 (12.5%)
AnomalyNumber of cases (%)
Congenital heart disease35 (39.8%)
Ventricular septal defect15 (17%)
Atrial septal defect12 (13.6%)
Musculoskeletal23 (26.1%)
Vertebral abnormality13 (14.8%)
Limb abnormality9 (10.2%)
Genitourinary26 (25%)
Renal abnormality21 (23.9%)
Genital/urinary abnormality5 (1.1%)
Intestinal7 (8%)
Imperforate anus5 (5.7%)
Atresia2 (2.3)
Intracranial/cranial facial9 (10.2%)
Craniofacial abnormality5 (5.7%)
Chromosomal8 (9.1%)
Trisomy 212 (2.3%)
VACTERL association11 (12.5%)
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