Delayed Onset of Lattice Corneal Dystrophy Type IIIA Due to a Novel T621P Mutation in TGFBI

J Refract Surg. 2016 May 1;32(5):356. doi: 10.3928/1081597X-20160225-01.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Cornea / diagnostic imaging
  • Cornea / pathology
  • Corneal Dystrophies, Hereditary / diagnosis
  • Corneal Dystrophies, Hereditary / genetics*
  • DNA Mutational Analysis
  • Exons / genetics
  • Extracellular Matrix Proteins / genetics*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pedigree
  • Point Mutation*
  • Proline / genetics
  • Threonine / genetics
  • Tomography, Optical Coherence
  • Transforming Growth Factor beta / genetics*
  • Visual Acuity

Substances

  • Extracellular Matrix Proteins
  • Transforming Growth Factor beta
  • betaIG-H3 protein
  • Threonine
  • Proline

Supplementary concepts

  • Corneal Dystrophy, Lattice Type IIIA