Corneal Dystrophy, Juvenile Epithelial of Meesmann
MESHD053559
An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder.
Synonyms
- Corneal Dystrophy, Meesmann Epithelial
- Meesmann Corneal Dystrophy
- Corneal Dystrophy, Meesmann
- Corneal Dystrophies, Meesmann
- Dystrophies, Meesmann Corneal
- Meesmann Corneal Dystrophies
- Meesmann Epithelial Corneal Dystrophy
- Juvenile Hereditary Epithelial Dystrophy
- Meesmann Corneal Epithelial Dystrophy
Source last updated 2026-05-24T15:24:51.397Z