| Literature DB >> 25193816 |
Arda Ozyuksel1, Cihangir Ersoy1, Emir Canturk1, Atif Akcevin1.
Abstract
Singleton Merten Syndrome is an autosomal dominant disorder of unknown origin. Patients often present with muscular weakness, failure to thrive, abnormal dentition, glaucoma, psoriatic skin lesions, aortic calcification and musculoskeletal abnormalities. In this case, we present a young girl with a history of aortic root replacement, who had an unusual progressive supra-aortic stenosis managed with urgent surgery during the course of the syndrome. Cardiovascular involvement needs special attention, since it is the major cause of mortality along with rhythm disturbances in the course of Singleton Merten Syndrome. 2014 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2014 PMID: 25193816 PMCID: PMC4158224 DOI: 10.1136/bcr-2014-205985
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X