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Meesmannova juvenilná epitelová dystrofia rohovky
Subject h. Meesmannova juvenilná epitelová dystrofia rohovky Subject h. Corneal Dystrophy, Juvenile Epithelial of Meesmann Entry terms dystrofia rohovky, juvenilná epitelová Meesmannova Scope note in English 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. 
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