Olmsted syndrome in an Indian male with a new de novo mutation in TRPV3

Br J Dermatol. 2016 Jan;174(1):209-11. doi: 10.1111/bjd.13910. Epub 2015 Nov 8.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Heterozygote
  • Humans
  • Keratoderma, Palmoplantar, Diffuse / genetics*
  • Male
  • Mutation / genetics*
  • Pedigree
  • Syndrome
  • TRPV Cation Channels / genetics*

Substances

  • TRPV Cation Channels
  • TRPV3 protein, human