Table 3 VACTERL-type and non-VACTERL-type malformations in three clusters of our cohort
From: Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?
Anomalies | Full phenotype | Partial phenotype | Non-VACTERL associated anomalies | |||
|---|---|---|---|---|---|---|
(15) | (6) | (4) | ||||
V | 10 | 66,6% | 1 | 16,6% | 0 | 0% |
A | 7 | 50% | 1 | 16,6% | 0 | 0% |
C | 10 | 71,4% | 3 | 50% | 0 | 0% |
TE | 14 | 100% | 6 | 100% | 4 | 100% |
R | 3 | 21,4% | 0 | 0% | 0 | 0% |
L | 6 | 42,8% | 1 | 16,6% | 0 | 0% |
SUA | 3 | 21,4% | 1 | 16,6% | 1 | 0% |
Duodenal atresia | 1 | 7% | 1 | 16,6% | 1 | 25% |
Cleft lip and palate | 2 | 14,2% | 0 | 0% | 0 | 0% |
Genital anomalies | 2 | 14,2% | 0 | 0% | 0 | 0% |
Hypothyroidism | 0 | 0% | 0 | 0% | 2 | 50% |
Vascular anomalies | 1 | 7% | 1 | 16,6% | 1 | 25% |
Nervous system anomalies | 3 | 21,4% | 1 | 16,6% | 0 | 0% |
Anomalies of toes | 2 | 14,2% | 2 | 33,3% | 0 | 0% |
Lower limb anomalies | 1 | 7% | 0 | 0% | 0 | 0% |