Table 3.

Proportions of VACTERL association in the EUROCAT database compared to those reported by Carter et al3 (i.e., only anomalies within the spectrum reported by Carter, et al with at least one record in the EUROCAT antiepileptic dataset).

Carter, et alEUROCAT Database
EUROCAT Subgroups*Major Congenital Anomalies without ChromosomalsProportion (%)All VACTERL Records without ChromosomalsProportion (%)Prevalence per 10,000 births
Total number in group3186,290
Nervous system13.281729.521.0
Neural tube defects13.236794.39.5
Anencephalus13.212701.53.3
Eye13.214271.73.7
Congenital cataract13.23390.40.9
Congenital heart disease722.626,65030.968.7
  Ventricular septal defect††13.211,97114.930.8
  Atrial septal defect††26.585099.922.0
  Tetralogy of Fallot††13.210031.22.6
Respiratory26.517232.04.4
Orofacial cleft13.260337.015.5
Cleft palate13.223692.76.2
Digestive system39.755016.414.2
  Esophageal atresia, ††13.29071.12.3
  Ano-rectal atresia and stenosis , ††13.210861.32.8
  Hirschsprung’s disease††13.23370.40.9
Urinary412.911,2011328.9
Genital39.770228.118.1
Hypospadia39.754906.414.1
Limb26.516,66219.343.0
Clubfoot without spina bifida13.238824.510.0
Musculoskeletal13.232393.88.3
  • * Only those subgroups in which Carter, et al had one or more congenital anomalies.

  • Anomaly belonging specifically to the VACTERL definition.

  • †† Subgroups of the main group of anomalies.