| Literature DB >> 20425839 |
Shobhit Madan1, Suneeta Madan-Khetarpal, Sang C Park, Urvashi Surti, Ariel L Bailey, Juliann McConnell, Sameh S Tadros.
Abstract
We report on a 22-year-old male carrying a presumptive clinical diagnosis of Dubowitz-like phenotype who has been followed-up by cardiology for bicuspid aortic valve with ascending aorta and aortic root dilatation. Cardiac magnetic resonance imaging (CMRI) confirmed these findings, along with an incidental finding of left ventricular non-compaction (LVNC). Genetic workup revealed the diagnosis of 22q11.2 distal deletion encompassing the BCR gene. This is the first time LVNC has been reported in a patient with 22q11.2 distal deletion. Copyright 2010 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2010 PMID: 20425839 DOI: 10.1002/ajmg.a.33367
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802