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 2024/04/19
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.