A rare, autosomal dominant inherited bilateral form of superficial corneal dystrophy, marked by symmetrical reticular opacities, and with the progressive impairment of vision. Corneal erosions manifest during childhood. The erosions develop in a honeycomb-like pattern in people in their 20s and 30s.

Also Known As

  • CDRB
  • Corneal Dystrophy Geographic
  • Corneal Dystrophy of Bowman Layer Type 1
  • Corneal Dystrophy Reis Bucklers Type
  • Reis Bucklers Dystrophy
  • Reis-Bucklers' Corneal Dystrophy
  • Granular Corneal Dystrophy Type III