Vacterl Association with Caudal Regression Syndrome and Complex CHD
Abstract: A rare case of a 1 year 7 months old boy presenting with multiple congenital anomalies including anorectal malformation, double outlet right ventricle with pulmonary atresia, bilateral hydronephrosis, and limb defects. The child fulfilled criteria for VACTERL association and also demonstrated features of caudal regression syndrome. He underwent multiple surgical interventions during infancy including staged anorectal reconstruction, PDA stenting, and colostomy closure. Despite ongoing supportive management, the child continued to experience cyanosis, recurrent urinary tract infections, and developmental delay. This report underscores the challenges of diagnosis and multidisciplinary care in children with overlapping syndromic anomalies.
Keywords: VACTERL, caudal regression syndrome, anorectal malformation, congenital heart disease, limb anomaly
How to Cite?: M. Kavimani, K. Girija, "Vacterl Association with Caudal Regression Syndrome and Complex CHD", Volume 14 Issue 10, October 2025, International Journal of Science and Research (IJSR), Pages: 231-232, https://www.ijsr.net/getabstract.php?paperid=SR251004115202, DOI: https://dx.doi.org/10.21275/SR251004115202