Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin

J Invest Dermatol. 2011 Mar;131(3):779-81. doi: 10.1038/jid.2010.363. Epub 2010 Dec 30.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Dermatitis, Exfoliative / diagnosis
  • Dermatitis, Exfoliative / genetics*
  • Diagnosis, Differential
  • Female
  • Glycoproteins / genetics*
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Male
  • Mutation / genetics
  • Netherton Syndrome / diagnosis
  • Netherton Syndrome / genetics
  • Pedigree
  • Polymorphism, Single Nucleotide / genetics*
  • Proteinase Inhibitory Proteins, Secretory / genetics
  • Serine Peptidase Inhibitor Kazal-Type 5

Substances

  • CDSN protein, human
  • Glycoproteins
  • Intercellular Signaling Peptides and Proteins
  • Proteinase Inhibitory Proteins, Secretory
  • SPINK5 protein, human
  • Serine Peptidase Inhibitor Kazal-Type 5