Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification. Abnormalities in different genes can cause a single phenotype, whereas different defects in a single gene can cause different phenotypes. Some disorders termed corneal dystrophies do not appear to have a genetic basis. Purpose: The purpose of this study was to develop a new classification system for corneal dystrophies, integrating up-to-date information on phenotypic description, pathologic examination, and genetic analysis. Methods: The International Committee for Classification of Corneal Dystrophies (IC3D) was created to devise a current and accurate nomenclature. Results: This anatomic classification continues to organize dystrophies according to the level chiefly affected. Each dystrophy has a template summarizing genetic, clinical, and pathologic information. A category number from 1 through 4 is assigned, reflecting the level of evidence supporting the existence of a given dystrophy. The most defined dystrophies belong to category 1 (a welldefined corneal dystrophy in which a gene has been mapped and identified and specific mutations are known) and the least defined belong to category 4 (a suspected dystrophy where the clinical and genetic evidence is not yet convincing). The nomenclature may be updated over time as new information regarding the dystrophies becomes available. Conclusions: The IC3D Classification of Corneal Dystrophies is a new classification system that incorporates many aspects of the traditional definitions of corneal dystrophies with new genetic, clinical, and pathologic information. Standardized templates provide key information that includes a level of evidence for there being a corneal dystrophy. The system is user-friendly and upgradeable and can be retrieved on the website www.corneasociety.org/ic3d. Copyright

Corneal dystrophy, Corneal histopathology, Epithelial basement membrane dystrophy, Epithelial recurrent erosion dystrophy, Eponym, Gene, Genetic corneal disease, Inherited corneal disease, Key reference, Mutation, Subepithelial mucinous corneal dystrophy
dx.doi.org/10.1097/ICO.0b013e31817780fb, hdl.handle.net/1765/61436
Cornea: the journal of cornea and external disease
Department of Ophthalmology

Weiss, J.S, Møller, H.U, Lisch, W, Kinoshita, E, Aldave, A.J, Belin, M.W, … Klintworth, G.K. (2008). The IC3D classification of the corneal dystrophies. Cornea: the journal of cornea and external disease, 27(SUPPL. 2). doi:10.1097/ICO.0b013e31817780fb