Abstract
A newborn diagnosed with severe aortic coarctation underwent surgical repair but developed re-coarctation and pulmonary artery narrowing. Persistent eyelid oedema and dysmorphic features led to a suspicion of Williams Syndrome, confirmed through genetic testing. This syndrome, caused by a chromosome 7 microdeletion, involves cardiovascular and multivessel abnormalities and necessitates close monitoring and prompt intervention.
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