Patent ductus arteriosus (PDA) and coarctation of the aorta (CoA) are relatively common congenital heart defects. Pathogenic variants in PRDM6, which encodes a smooth-muscle-cell-specific transcription factor, have now been etiologically associated with non-syndromic PDA. We present three patients with PDA and CoA found to harbor PRDM6 variants, including a novel, likely-pathogenic variant.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/ajmg.a.63500 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!