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-12Lecithin Acyltransferase DeficiencyVisual AcuityExtracellular Matrix ProteinsBowman MembraneEye DiseasesEndothelium, CornealMuscular Dystrophy, AnimalBlindnessEntropionSurgery, PlasticTrachomaEyelid DiseasesKeratoconusTattooingLasers, ExcimerDNA Mutational AnalysisAmyloidosis, FamilialKeratoconjunctivitisEpithelium, CornealPupil DisordersEye BurnsBurns, ChemicalMutationEstheticsCorneal PachymetryMicroscopy, AcousticCurrent Procedural TerminologyRetinal DystrophiesDimethylallyltranstransferaseTransforming Growth Factor betaMuscular Dystrophy, FacioscapulohumeralEye AbnormalitiesCorneal NeovascularizationKeratin-3KeratitisMutation, MissenseVision, LowDystrophinCorneal EdemaExonsHeterozygoteAnterior Eye SegmentSulfotransferasesPhenotypeLens Nucleus, CrystallineChromosomes, Human, Pair 5Keratitis, HerpeticLens Cortex, CrystallineVision DisordersGenes, DominantEye ProteinsGenetic LinkageMuscular Dystrophy, Emery-DreifussMice, Inbred mdxHomozygoteBase SequenceContact LensesCorneal TopographyNeuroaxonal DystrophiesEyeChromosomes, Human, Pair 20AmyloidosisMolecular Sequence DataPolymerase Chain ReactionAsian Continental Ancestry GroupSarcoglycansMicroscopy, Confocal