Meesmann Corneal Dystrophy

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant inherited corneal disorder caused by mutations in the KRT3 and KRT12 genes. It is characterized by the formation of multiple tiny cysts in the epithelial layer of the cornea. The cysts may rupture, causing pain, redness and light sensitivity. Vision usually is not affected.

**Synonyms:** - Juvenile Epithelial of Meesmann Corneal Dystrophy