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Ann Thorac Surg ; 101(1): 359-61, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26694280

ABSTRACT

Williams syndrome (WS) is a genetic disorder due to deficiency of elastin gene expression. It is characterized by typical somatic abnormalities and a wide range of cardiovascular malformations. Coronary artery involvement is a frequent finding of the syndrome, particularly in those patients with severe supravalvular aortic stenosis. We present the case of an 11-month-old infant affected by WS who developed severe coronary artery disease 2 months after the surgical repair of supravalvular aortic stenosis. The clinical picture and successful surgical revascularization strategy is also described.


Subject(s)
Coronary Artery Bypass/methods , Coronary Stenosis/etiology , Coronary Vessels/surgery , Williams Syndrome/complications , Coronary Stenosis/diagnosis , Coronary Stenosis/surgery , Echocardiography , Electrocardiography , Humans , Infant , Male , Tomography, X-Ray Computed , Williams Syndrome/surgery
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