Williams syndrome and obstructed total anomalous pulmonary venous return: a previously unreported association

Han Ki Park; Jeffrey S Heinle; David L S Morales

doi:10.1016/j.athoracsur.2011.11.063

Williams syndrome and obstructed total anomalous pulmonary venous return: a previously unreported association

Ann Thorac Surg. 2012 Jul;94(1):289-91. doi: 10.1016/j.athoracsur.2011.11.063.

Authors

Han Ki Park¹, Jeffrey S Heinle, David L S Morales

Affiliation

¹ Division of Congenital Heart Surgery, Department of Surgery, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas 77030, USA.

PMID: 22734998
DOI: 10.1016/j.athoracsur.2011.11.063

Abstract

We report a case of a neonate who presented with obstructed mixed total anomalous pulmonary venous return (TAPVR) and Williams syndrome. After initial repair of TAPVR, his aortic wall continued to thicken, resulting in aortic arch hypoplasia and near atresia of the entire course of the left main coronary artery requiring a novel type of repair at 5 months of age. Cardiovascular abnormalities are frequently associated with Williams syndrome. This is a report of a rare patient with both Williams syndrome and obstructed TAPVR.

Publication types

Case Reports

MeSH terms

Humans
Infant, Newborn
Magnetic Resonance Imaging
Male
Scimitar Syndrome / complications*
Scimitar Syndrome / pathology
Scimitar Syndrome / surgery
Williams Syndrome / complications*
Williams Syndrome / pathology
Williams Syndrome / surgery