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Coronary Artery Involvement of Williams Syndrome in Infants and Surgical Revascularization Strategy
Duccio Federici1, Arianna Ranghetti2, Maurizio Merlo1
1Cardiac Surgery Unit, "Papa Giovanni XXIII" Hospital, Bergamo, Italy.
Insights
Williams syndrome (WS), a genetic disorder affecting elastin, can cause severe coronary artery disease after surgery for supravalvular aortic stenosis. This case highlights successful revascularization in an infant with WS.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Pediatric Surgery
Background:
- Williams syndrome (WS) is a genetic disorder characterized by elastin deficiency, leading to diverse somatic and cardiovascular abnormalities.
- Coronary artery disease is a common complication in WS, especially with supravalvular aortic stenosis.
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.
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