Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals

J Invest Dermatol. 2010 Jun;130(6):1741-6. doi: 10.1038/jid.2010.23. Epub 2010 Feb 18.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Blister / genetics
  • Blister / pathology
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Diagnosis, Differential
  • Epidermolysis Bullosa / diagnosis*
  • Epidermolysis Bullosa / genetics*
  • Epidermolysis Bullosa / pathology
  • Erythema / genetics
  • Erythema / pathology
  • Humans
  • Infant
  • Infant, Newborn
  • Mutation, Missense / genetics*
  • Skin / pathology
  • Skin Aging / genetics
  • Skin Aging / pathology
  • Skin Diseases / diagnosis*
  • Skin Diseases / genetics*
  • Skin Diseases / pathology
  • Syndrome
  • Transglutaminases / genetics*
  • Young Adult

Substances

  • transglutaminase 5
  • Transglutaminases