| Literature DB >> 22981642 |
E Gok1, O S Goksel, U Alpagut, E Dayioglu.
Abstract
The Ehlers-Danlos Syndrome (EDS) is a rare connective tissue disorder characterised by fragility of the soft connective tissues and widespread manifestations in skin, ligaments, joints, blood vessels and internal organs. We report a case of a 12-year-old boy, previously diagnosed with kyphoscoliosis-type EDS (type VI), presenting with a left brachial artery pseudo-aneursym with history of multiple spontaneous and post-traumatic arterial ruptures. Surgical management of this patient was performed successfully by primary repair of brachial artery lesion.Entities:
Mesh:
Year: 2012 PMID: 22981642 DOI: 10.1016/j.ejvs.2012.08.004
Source DB: PubMed Journal: Eur J Vasc Endovasc Surg ISSN: 1078-5884 Impact factor: 7.069