Abstract
Skeletal anomalies are seen in 1.6–55 % of cases of esophageal atresia or tracheoesophageal fistula, usually in the context of the VACTERL association, and may be divided into limb and spinal anomalies. The most common limb anomaly is radial defect/hypoplasia. Congenital spine anomalies may lead to scoliosis, although deformity may also result iatrogenically after thoracotomy. Life expectancy mainly depends on the degree of nonskeletal involvement. Associated skeletal anomalies are typically non-life-threatening, and treatment of such may thus be delayed until medical stabilization is performed and a better understanding of overall prognosis is obtained. For patients with minimal symptoms or limitations secondary to nonskeletal anomalies, the results of treatment of their skeletal anomalies are dependent on the degree of involvement and type of malformation and are expected to be the same as if they occurred in isolated fashion.
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Sembrano, J.N., Truong, W.H., Ledonio, C.G.T., Polly, D.W. (2017). Skeletal Anomalies Associated with Esophageal Atresia. In: Till, H., Thomson, M., Foker, J., Holcomb III, G., Khan, K. (eds) Esophageal and Gastric Disorders in Infancy and Childhood. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-11202-7_11
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DOI: https://doi.org/10.1007/978-3-642-11202-7_11
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