Emerging genes implicated in human congenital heart disease: a 2023–2025 scoping review

Abstract excerpt

Background: Congenital heart disease (CHD) is the most common major congenital anomaly and a leading cause of infant morbidity and mortality. The rapid expansion of genomic technologies has accelerated the discovery of rare genetic variants implicated in CHD pathogenesis. However, most individuals with CHD still lack an identifiable molecular etiology. The purpose of this scoping review is to systematically charac...

Topics

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• Congenital heart defects research
• Congenital Heart Disease Studies
• Genomics and Rare Diseases

Identifiers and source

Literature Corpus work

302d5928-b1c6-5a7c-af36-591337c6c94c

DOI

10.21037/tp-2026-0487