Schöpf-Schulz-Passarge syndrome

Br J Dermatol. 1992 Jul;127(1):33-5. doi: 10.1111/j.1365-2133.1992.tb14822.x.

Abstract

Three siblings, the children of a marriage between first cousins, are reported with the characteristic ophthalmological and cutaneous changes of the Schöpf-Schulz-Passarge syndrome. There have been only eight reported cases of this disorder, and it has not previously been described in Great Britain.

Publication types

  • Case Reports

MeSH terms

  • Cysts / epidemiology
  • Cysts / genetics*
  • Ectodermal Dysplasia / epidemiology
  • Ectodermal Dysplasia / genetics*
  • Eyelid Diseases / epidemiology
  • Eyelid Diseases / genetics*
  • Facial Expression
  • Family
  • Female
  • Humans
  • Hypotrichosis / epidemiology
  • Hypotrichosis / genetics
  • Male
  • Middle Aged
  • Nails, Malformed*
  • Syndrome
  • United Kingdom / epidemiology