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WBS is a rare disorder caused by mutations in the chromosomal sub‐band 7q11.23 involving the elastin gene. The clinical features (craniofacial, developmental, and cardiovascular abnormalities) are variable. The association with cardiac anomalies is a well‐recognized feature, and SVAS is the most common cardiac defect found. End‐stage ischemic heart disease is unusual in this setting but when it occurs,...
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