John Libbey Eurotext

European Journal of Dermatology

CarpeDIEM – Dermatological Indications for Electron Microscopy: Ehlers Danlos Syndrome Volume 21, numéro 6, November-December 2011

ejd.2011.1607 Auteur(s) : Emmanuella Guenova1, Martin Schaller1 1 Department of Dermatology, Eberhard Karls University Tübingen, 72076 Tübingen, Germany Ehlers Danlos Syndrome is a group of rare inherited connective tissue disorders, comprising six major and several minor types of the disease. Common clinical symptoms of Ehlers Danlos Syndrome include easy bruising, excessive scarring, and poor wound healing. Furthermore, pathologically increased mobility of the joints, joint dislocation, and...