Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations

Br J Dermatol. 2014 Sep;171(3):675-8. doi: 10.1111/bjd.12951. Epub 2014 Aug 4.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Child
  • Erythromelalgia / genetics*
  • Hair Diseases / genetics
  • Humans
  • Hyperhidrosis / genetics
  • Keratoderma, Palmoplantar / genetics*
  • Keratosis / genetics*
  • Male
  • Mutation, Missense / genetics*
  • Syndrome
  • TRPV Cation Channels / genetics*

Substances

  • TRPV Cation Channels
  • TRPV3 protein, human