Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve.

ABSTRACT:

Background

Bicuspid aortic valve (BAV) is the most common congenital heart defect in adults, often leading to complications such as thoracic aortic aneurysms and aortic stenosis. While BAV is frequently associated with 22q11.2 deletion syndrome (22q11.2DS), the contribution of rare copy number variants (CNVs) in this region to non-syndromic BAV is less clear. This study is aimed to assess the role of rare 22q11.2 CNVs in patients with early-onset BAV (EBAV) and to determine whether these variants are linked to an increased risk of complications.

Methods

Whole genome microarray genotyping was conducted on 272 patients with BAV with early onset valve or aortic disease (EBAV) and 272 biological relatives. CNVs were detected using three independent algorithms, focusing on the 22

SUBMITTER: DiGregorio H 

PROVIDER: S-EPMC11821425 | biostudies-literature | 2025 Feb

REPOSITORIES: biostudies-literature