Congenital heart disease presentations in the 15q11.2 microdeletion syndrome

Congenital heart disease presentations in the 15q11.2 microdeletion syndrome

Congenital heart disease (CHD) is the most common type of birth defect and results from anomalies in the cardiogenesis process. There are multiple genetic mechanisms contributing to CHD, including copy number variants (CNVs). One such CNV is the 15q11.2 (BP1-BP2) microdeletion, which contains four e...

Full description

Saved in:
Bibliographic Details
Main Authors: Claudia-Ioana Fifirig, Sabu Abraham, Bernard Keavney, Kathryn E. Hentges
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Genetics
Subjects:
congenital heart disease
genetics
development
BP1-BP2/15q11.2 deletion syndrome
copy number variant
phenotypic heterogeneity
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2025.1535732/full
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2025.1535732/full

Similar Items