Asociación inusual en el síndrome de Brachmann-de Lange

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Brachmann-de Lange syndrome is a low incidence multiple congenital anomaly syndrome that includes a wide range of congenital heart diseases. We present a patient diagnosed with aortic coarctation during adulthood, who was subjected to surgical closure of ductus arteriosus and pulmonary valvotomy during the neonatal period. To our knowledge the combination of patent ductus arteriosus, pulmonary stenosis, and aortic coarctation in Brachmann-de Lange syndrome has not been previously described.