Corneal OpacityCorneal Dystrophies, HereditaryFuchs' Endothelial DystrophyCorneaCorneal Dystrophy, Juvenile Epithelial of MeesmannMuscular DystrophiesCollagen Type VIIIMyotonic DystrophyKeratoplasty, PenetratingEyelashesCorneal StromaCorneal DiseasesMuscular Dystrophy, DuchenneTrichiasisPedigreeKeratan SulfateCataractHair RemovalDescemet MembraneCorneal KeratocytesPhotorefractive KeratectomyCorneal TransplantationKeratin-12Visual AcuityLecithin Acyltransferase DeficiencyExtracellular Matrix ProteinsEndothelium, CornealBowman MembraneEye DiseasesMuscular Dystrophy, AnimalBlindnessEntropionSurgery, PlasticGraft SurvivalTrachomaEyelid DiseasesKeratoconusTattooingLasers, ExcimerDNA Mutational AnalysisAmyloidosis, FamilialEpithelium, CornealKeratoconjunctivitisPupil DisordersEye BurnsBurns, ChemicalEstheticsMutationCorneal PachymetryMicroscopy, AcousticCurrent Procedural TerminologyRetinal DystrophiesTransforming Growth Factor betaDimethylallyltranstransferaseCorneal NeovascularizationMuscular Dystrophy, FacioscapulohumeralEye AbnormalitiesKeratitisKeratin-3Mutation, MissenseGraft Occlusion, VascularVision, LowDystrophinCorneal EdemaExonsHeterozygoteAnterior Eye SegmentSulfotransferasesPhenotypeLens Nucleus, CrystallineChromosomes, Human, Pair 5Keratitis, HerpeticLens Cortex, CrystallineVision DisordersGenes, DominantEye ProteinsGenetic LinkageMuscular Dystrophy, Emery-DreifussMice, Inbred mdxHomozygoteBase SequenceContact LensesCorneal TopographyEyeNeuroaxonal DystrophiesPolymerase Chain ReactionChromosomes, Human, Pair 20AmyloidosisMolecular Sequence DataAsian Continental Ancestry GroupSarcoglycansMicroscopy, Confocal