MODY 3

This is the most common type of MODY in populations with European ancestry,[1] accounting for about 70% of all cases in Europe.This is the form of MODY which can most resemble diabetes mellitus type 1, and one of the incentives for diagnosing it is that insulin may be discontinued or deferred in favor of oral sulfonylureas.Some people treated with insulin for years due to a presumption of type 1 diabetes have been able to switch to oral medication and discontinue injections.Long-term diabetic complications can occur if blood glucose levels are not adequately controlled.High-sensitivity measurements of C-reactive protein may help to distinguish between HNF1A-MODY and other forms of diabetes [2] This article about an endocrine, nutritional, or metabolic disease is a stub.

maturity-onset diabetes of the youngHNF1-alphahomeoboxhuman chromosome 12beta cellsMODY 1diabetes mellitus type 1C-reactive proteinpancreasglucose metabolismDiabetestype 1type 2gestationalComplicationsblood glucoseHyperglycemiaOxyhyperglycemiaHypoglycemiaWhipple's triadInsulinInsulin resistanceHyperinsulinismCongenital hyperinsulinismRabson–Mendenhall syndromePancreatic beta cell functionInsulinomaInsulitisGenetic disorderstranscription factorFeingold syndromeSaethre–Chotzen syndromeTietz syndromeIntracellular receptorThyroid hormone resistanceAndrogen insensitivity syndromeKennedy's diseasePHA1AD pseudohypoaldosteronismEstrogen insensitivity syndromeX-linked adrenal hypoplasia congenitaFamilial partial lipodystrophy 3SF1 XY gonadal dysgenesisBarakat syndromeTricho–rhino–phalangeal syndromeGreig cephalopolysyndactyly syndromePallister–Hall syndromeDenys–Drash syndromeDuane-radial ray syndromeMODY 7MRX 89Townes–Brocks syndromeAcrocallosal syndromeMyotonic dystrophy 2Autoimmune polyendocrine syndrome type 1Ohtahara syndromeLissencephaly X2Currarino syndromeHOXD13SPD1 synpolydactylyMODY 4Nail–patella syndromeTooth and nail syndromeAxenfeld syndrome 1POU4F3DFNA15POU3F4Posterior polymorphous corneal dystrophyFuchs' dystrophy 3Mowat–Wilson syndromePapillorenal syndromeWaardenburg syndrome 1&3MODY 9Gillespie syndromeColoboma of optic nerveCongenital hypothyroidism 2STHAG3Axenfeld syndrome 3Iridogoniodysgenesis, dominant typeLymphedema–distichiasis syndromeBamforth–Lazarus syndromeAnterior segment mesenchymal dysgenesisACD/MPVEnlarged vestibular aqueductPremature ovarian failure 3Van der Woude syndromePopliteal pterygium syndromeHyperimmunoglobulin E syndromeHolt–Oram syndromeLi–Fraumeni syndromeUlnar–mammary syndromeCampomelic dysplasiaMODY 5SRY XY gonadal dysgenesisPremature ovarian failure 7Waardenburg syndrome 4cYemenite deaf-blind hypopigmentation syndromeCleidocranial dysostosisKabuki syndromePitt–Hopkins syndromeRapp–Hodgkin syndromeHay–Wells syndromeEctrodactyly–ectodermal dysplasia–cleft syndrome 3Limb–mammary syndromeTranscription coregulatorsCREBBPRubinstein–Taybi syndromeAtrichia with papular lesions