A syndrome of keratosis palmo-plantaris congenita, pes planus, onychogryphosis, periodontosis, arachnodactyly and a peculiar acro-osteolysis

Br J Dermatol. 1986 Aug;115(2):243-8. doi: 10.1111/j.1365-2133.1986.tb05725.x.

Abstract

A family with a symptom complex of pes planus, onychogryphosis, palmoplantar hyperkeratosis and periodontosis is reported. A detailed pedigree is given and the mode of inheritance is suggested.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Aggressive Periodontitis / genetics*
  • Bone Resorption / genetics*
  • Child
  • Child, Preschool
  • Female
  • Flatfoot / genetics*
  • Humans
  • Keratoderma, Palmoplantar / congenital*
  • Male
  • Marfan Syndrome / genetics*
  • Nail Diseases / genetics*
  • Osteolysis / genetics*
  • Pedigree
  • Periodontal Diseases / genetics*
  • Syndrome