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The purpose of this study was to report the association of phenotypic features characteristic of lattice corneal dystrophy (LCD) with a monoclonal gammopathy of undetermined significance (MGUS) after exclusion of a coding region mutation in transforming growth factor beta-induced (TGFBI) gene.

Classic Lattice Corneal Dystrophy Associated With Monoclonal Gammopathy After Exclusion of a TGFBI Mutation