Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation

Br J Ophthalmol. 2005 Nov;89(11):1538-40. doi: 10.1136/bjo.2005.073510.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Cornea / abnormalities*
  • Corneal Diseases / genetics*
  • Eye Diseases, Hereditary / genetics*
  • Eye Proteins / genetics
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Pedigree
  • Proteoglycans / genetics*

Substances

  • Eye Proteins
  • KERA protein, human
  • Proteoglycans