Diabetic AngiopathiesSyndromeDiabetes Mellitus, Type 1Diabetes MellitusDiabetes Mellitus, Type 2Ehlers-Danlos SyndromeUsher SyndromesOrofaciodigital SyndromesDiabetes Mellitus, ExperimentalPolyendocrinopathies, AutoimmuneDiabetic RetinopathyDiabetic NephropathiesReflex Sympathetic DystrophyDiabetes ComplicationsWaardenburg SyndromeCrigler-Najjar SyndromeMucopolysaccharidosis IIIHermanski-Pudlak SyndromeBlood GlucoseCongenital Disorders of GlycosylationDiabetic FootPregnancy in DiabeticsMetabolic Syndrome XPhosphotransferases (Phosphomutases)InsulinHemoglobin A, GlycosylatedPedigreeHypoglycemic AgentsStreptozocinAbnormalities, MultipleDown SyndromeMutationAddison DiseaseDiabetes, GestationalRetinitis PigmentosaLong QT SyndromeHearing Loss, SensorineuralHyperglycemiaBartter SyndromeRisk FactorsCardio-Renal SyndromeMannose-6-Phosphate IsomeraseLanger-Giedion SyndromePhenotypeAdaptor Protein Complex beta SubunitsDNA Mutational AnalysisDeafnessPiebaldismNephrotic SyndromeDiabetic CardiomyopathiesMice, Inbred NODSjogren's SyndromeDisease Models, AnimalDiabetic DietAlbuminuriaHypopigmentationTime FactorsCausalgiaIslets of LangerhansMutation, MissenseDiabetes InsipidusPigmentation DisordersInsulin ResistanceGlucose Tolerance TestTreatment OutcomeObesityAdaptor Protein Complex 3HomozygoteHeterozygoteMolecular Sequence DataLoeys-Dietz SyndromeFollow-Up StudiesPrevalenceGenotypeExonsGlucoseAcetylglucosaminidaseCollagen Type IIIGenetic LinkageProcollagenShort Rib-Polydactyly SyndromeAutoantibodiesCohort StudiesTurner SyndromeBase SequenceNeurophysiological MonitoringPrediabetic StateCase-Control StudiesAllelesSOXE Transcription FactorsProspective StudiesConsanguinityCodon, NonsenseGenetic Predisposition to DiseaseInsulin-Secreting CellsBody Mass IndexHaplotypesReference ValuesBiological MarkersSkin