Article

Advancing precision medicine in the Cardiac Intensive Care Unit using universal whole-genome sequencing

2026-05-14

Abstract excerpt

Congenital heart defects (CHD) are a common congenital anomaly and a leading cause of neonatal mortality. Even in ostensibly isolated cases, genetic testing can reveal monogenic causes of isolated CHD or identify syndromic conditions before additional features become clinically apparent. A timely and accurate genetic diagnosis can inform medical management and surveillance, reduce the need for unnecessary investig...

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Literature Corpus work: 809500d0-63f0-5252-8ea0-653767ae5827
DOI: 10.64898/2026.05.11.26352916

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