RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164069017 T1 Epidermolysis Bullosa T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164069017 RD 2024/10/07 AB It is defined as a group of genetically inherited connective tissue disorders characterized by cutaneous blistering of the skin and mucosal membranes after minor trauma. The lesions heal with severe scarring. It results from a membrane defect located between the epidermis and the dermis as a result of external shearing forces applied to the skin, such as simple friction. Its severity ranges from mild to lethal.