Diseases [C] » Eye Diseases [C11] » Corneal Diseases » Corneal Dystrophies, Hereditary » Corneal Dystrophy, Juvenile Epithelial of Meesmann
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Corneal Dystrophies, Hereditary » Corneal Dystrophy, Juvenile Epithelial of Meesmann
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Corneal Dystrophies, Hereditary » Corneal Dystrophy, Juvenile Epithelial of Meesmann
Description
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. MeSH
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