Corneal Dystrophies, HereditaryCorneal OpacityFuchs' Endothelial DystrophyCorneal Dystrophy, Juvenile Epithelial of MeesmannMuscular DystrophiesCollagen Type VIIICorneaMyotonic DystrophyMuscular Dystrophy, DuchenneKeratoplasty, PenetratingPedigreeCorneal StromaDescemet MembraneKeratan SulfateKeratin-12Corneal DiseasesExtracellular Matrix ProteinsBowman MembraneMuscular Dystrophy, AnimalEndothelium, CornealCorneal TransplantationKeratoconusEyelashesAmyloidosis, FamilialDNA Mutational AnalysisCorneal KeratocytesPhotorefractive KeratectomyTrichiasisVisual AcuityCataractMutationLasers, ExcimerHair RemovalCorneal PachymetryEpithelium, CornealCurrent Procedural TerminologyRetinal DystrophiesEye DiseasesDimethylallyltranstransferaseTransforming Growth Factor betaMuscular Dystrophy, FacioscapulohumeralKeratin-3DystrophinMutation, MissenseLecithin Acyltransferase DeficiencyExonsBlindnessHeterozygoteSulfotransferasesEntropionCorneal EdemaPhenotypeChromosomes, Human, Pair 5Surgery, PlasticTrachomaEyelid DiseasesTattooingGenes, DominantKeratoconjunctivitisMuscular Dystrophy, Emery-DreifussGenetic LinkageEye ProteinsMice, Inbred mdxPupil DisordersHomozygoteEye BurnsBase SequenceBurns, ChemicalNeuroaxonal DystrophiesChromosomes, Human, Pair 20AmyloidosisEstheticsCorneal TopographyMicroscopy, AcousticPolymerase Chain ReactionSarcoglycansMolecular Sequence DataAsian Continental Ancestry GroupEye AbnormalitiesMicroscopy, ConfocalKeratitisVision, LowCorneal NeovascularizationAnion Transport ProteinsAmino Acid SubstitutionAnterior Eye SegmentPoint MutationTransforming Growth Factor beta1Muscular Dystrophy, OculopharyngealConsanguinityGenetic HeterogeneityDystroglycansCzech RepublicReflex Sympathetic DystrophyLens Nucleus, CrystallineKeratitis, HerpeticFrameshift MutationPolymorphism, Single-Stranded ConformationalGenetic Association StudiesUtrophin