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. 2022 Nov 24;9(12):1814. doi: 10.3390/children9121814

Table 2.

Overview of associated anomalies.

Type of Anomaly Total N = 112 (%) Atresia N = 41 Annular Pancreas N = 34 Web/Membrane N = 37
Number of associated anomalies 53 (47%) 17 (42%) 14 (41%) 22 (60%)
Single 33 (68%) 9 (53%) 8 (57%) 16 (73%)
Multiple 20 (32%) 8 (47%) 6 (43%) 6 (27%)
Cardiovascular 35 (31%) 8 (20%) 11 (32%) 16 (43%)
Atrial septal defect 7 (20%) 1 2 4
Ventricular septal defect 6 (17%) 2 2 2
Atrioventricular septal defect 13 (37%) 1 6 6
Tetralogy of Fallot 3 (9%) 1 1 1
Persistent ductus arteriosus 3 (9%) 1 0 2
Kommerell diverticula 1 (3%) 1 0 0
Isomerism of atrial appendages 2 (6%) 1 0 1
Vertebral 12 (11%) 5 (12%) 3 (9%) 4 (11%)
Scoliosis 4 (33%) 2 1 1
Sacral anomaly 3 (25%) 2 0 1
Anomaly of vertebrae 5 (42%) 3 1 1
Deviating amount of ribs 3 (25%) 0 2 1
Renal 6 (5%) 1 (2%) 4 (12%) 1 (3%)
Pelviureteric junction stenosis 1 (16.6%) 1 0 0
Mono kidney 1 (16.6%) 0 1 0
Horseshoe kidney 1 (16.6%) 0 1 0
Lobulated kidney 1 (16.6%) 0 1 0
Shriveled kidney 1 (16.6%) 0 1 0
Extra renal pyelum 1 (16.6%) 0 0 1
Genito-urinary tract 5 (5%) 1 (2%) 2 (6%) 2 (5%)
Hypospadia 2 (40%) 0 1 1
Uretral obstruction 1 (20%) 0 0 1
Neurogenic bladder in ARM 2 (40%) 1 1 0
Eye, ear and neck 7 (6%) 1 (2%) 1 (3%) 5 (13%)
Hearing loss 6 (86%) 1 1 4
Nystagmus 1 (14%) 0 0 1
Esophageal 3 (3%) 3 (7%) 0 (0%) 0 (0%)
Esophageal atresia with fistula 3 (100%) 3 0 0
Respiratory tract 10 (9%) 3 (7%) 2 (6%) 5 (14%)
Tracheomalacia 3 (30%) 1 0 2
Bronchomalacia 4 (40%) 1 1 2
Tracheobronchomalacia 2 (20%) 0 1 1
Pulmonary hypertension 1 (10%) 1 0 0
Anus 5 (5%) 3 (7%) 1 (3%) 1 (3%)
Anorectal malformation 5 (100%) 3 1 1
Limbs 10 (9%) 4 (10%) 3 (9%) 3 (8%)
Syndactyly 1 (10%) 1 0 0
Clinodactyly 1 (10%) 1 0 0
Anomaly of the thumb 3 (30%) 0 2 1
Hypoplasia forearm 2 (20%) 1 1 0
Clubfoot 2 (20%) 0 0 2
Cleft, lip and palate 1 (1%) 0 (0%) 0 (0%) 1 (3%)
Palatoschisis 1 (100%) 0 0 1
Nervous system 2 (2%) 1 (2%) 0 (0%) 1 (3%)
Microcephaly 2 (100%) 1 0 1
Other 2 (2%) 1 (2%) 0 (0%) 1 (3%)
Polysplenia 2 (100%) 1 0 1
Genetics 42 (38%) 10 (24%) 14 (41%) 19 (50%)
Trisomy 21 35 (85.6%) 9 13 15
Fanconi syndrome 1 0 0 1
Feingold syndrome 1 1 0 0
Cornelia de Lange syndrome 1 0 1 0
22q11 microdeletion 1 0 0 1
Heterotaxie syndrome 1 0 0 1
MCT1 gene defect 1 0 0 1
VACTERL association 4 (4%) 2 (5%) 1 (3%) 1 (3%)
STRICT-VACTERL 1 (25%) 1 0 0
VACTERL-LIKE 3 (75%) 1 1 1
VACTERL-PLUS 0 (0%) 0 0 0

N = Number. ARM = anorectal malformation. VACTERL = vertebral anomalies, anal atresia, cardiac anomalies, tracheo-esophageal fistula, renal anomalies, limb abnormalities [10].