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

Authors
 Han Ki Park  ;  Jeffrey S. Heinle  ;  David L.S. Morales 
Citation
 ANNALS OF THORACIC SURGERY, Vol.94(1) : 289-291, 2012 
Journal Title
 ANNALS OF THORACIC SURGERY 
ISSN
 0003-4975 
Issue Date
2012
MeSH
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
Keywords
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
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.
Full Text
http://www.sciencedirect.com/science/article/pii/S0003497511028190
DOI
22734998
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Thoracic and Cardiovascular Surgery (흉부외과학교실) > 1. Journal Papers
Yonsei Authors
Park, Han Ki(박한기) ORCID logo https://orcid.org/0000-0002-7472-7822
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/89567
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