Gelatinous drop-like corneal dystrophy is not one of the beta ig-h3-mutated corneal amyloidoses

Am J Ophthalmol. 1998 Dec;126(6):832-3. doi: 10.1016/s0002-9394(98)00186-x.

Abstract

Purpose: To discover if beta ig-h3 is mutated in gelatinous drop-like corneal dystrophy, as has been suggested.

Methods: Genomic DNA was isolated from unrelated individuals with lattice corneal dystrophy type I (n = 3), Avellino corneal dystrophy (n = 3), and gelatinous drop-like corneal dystrophy (n = 3) and used as a template for polymerase chain reaction to amplify all exons in beta ig-h3. The polymerase chain reaction product was then sequenced.

Results: Beta ig-h3 is mutated in lattice corneal dystrophy type I (Arg124Cys) and Avellino corneal dystrophy (Arg124His). In gelatinous drop-like corneal dystrophy, on the other hand, no mutation was detected in the entire coding region of beta ig-h3 (all 17 exons).

Conclusion: Unlike the amyloidotic corneal dystrophies lattice type I and Avellino, gelatinous drop-like corneal dystrophy is not likely to be caused by a mutation in beta ig-h3.

MeSH terms

  • Amyloidosis / genetics*
  • Cornea / pathology
  • Corneal Dystrophies, Hereditary / genetics*
  • Corneal Dystrophies, Hereditary / pathology
  • DNA Mutational Analysis
  • Exons / genetics
  • Extracellular Matrix Proteins*
  • Humans
  • Mutation*
  • Neoplasm Proteins / genetics*
  • Polymerase Chain Reaction
  • Transforming Growth Factor beta / genetics*

Substances

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