A case of complete form of pachydermoperiostosis with SLCO2A1 mutations

Eur J Dermatol. 2021 Apr 1;31(2):249-251. doi: 10.1684/ejd.2021.4003.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Heterozygote
  • Humans
  • Male
  • Mutation
  • Organic Anion Transporters / genetics*
  • Osteoarthropathy, Primary Hypertrophic / diagnosis*
  • Osteoarthropathy, Primary Hypertrophic / diagnostic imaging
  • Osteoarthropathy, Primary Hypertrophic / genetics*
  • Radiography

Substances

  • Organic Anion Transporters
  • SLCO2A1 protein, human