A novel mutation in CDSN causes peeling skin disease in a patient from Morocco

Br J Dermatol. 2011 Nov;165(5):1152-5. doi: 10.1111/j.1365-2133.2011.10529.x.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Consanguinity
  • Dermatitis, Exfoliative / genetics*
  • Female
  • Frameshift Mutation / genetics*
  • Glycoproteins / deficiency
  • Glycoproteins / genetics*
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Pigmentation Disorders / genetics*
  • Polymorphism, Single Nucleotide
  • Skin Diseases / congenital

Substances

  • CDSN protein, human
  • Glycoproteins
  • Intercellular Signaling Peptides and Proteins

Supplementary concepts

  • Peeling skin syndrome, acral type