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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Postoperative morbidity and health-related quality of life in children with delayed reconstruction of esophageal atresia: a nationwide Swedish study

Fig. 2

Symptom prevalence and treatments at follow up in children aged 2–7 (Fig. 2a) and in children aged 8–18 (Fig. 2b) with delayed reconstruction of esophageal atresia compared to children with esophageal atresia Gross type C who underwent primary anastomosis. The statistical comparison was performed using Fisher’s exact test. Significant level was p < 0.05. Significant p-values are marked with bold text

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