ⓘ Dentin dysplasia

                                     

ⓘ Dentin dysplasia

Dentin dysplasia is a rare genetic developmental disorder dentine production of the teeth, commonly exhibiting an autosomal dominant inheritance that causes malformation of the root. It affects both primary and permanent dentitions in approximately 1 in every 100.000 patients. It is characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology. Witkop in 1972 classified DD into two types which are Type I is the radicular type, and type II is the coronal type. DD-1 has been further divided into 4 different subtypes based on the radiographic features.

                                     
  • mapping of the human dentin sialophosphoprotein DSPP gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci Eur
  • genetic disorder of tooth development. This condition is a type of dentin dysplasia that causes teeth to be discolored most often a blue - gray or yellow - brown
  • especially evident in coronal dentin near the DEJ, and in certain dental anomalies, such as in dentin dysplasia Secondary dentin is formed after root formation
  • Dentatorubral - pallidoluysian atrophy Dentin dysplasia sclerotic bones Dentin dysplasia coronal Dentin dysplasia radicular Dentinogenesis imperfecta
  • association with pulpal calcifications. Several genetic diseases such as dentin dysplasia and dentinogenesis imperfecta are also accompanied by pulpal calcifications
  • Dentin hypersensitivity DH, DHS is dental pain which is sharp in character and of short duration, arising from exposed dentin surfaces in response to
  • Ectrodactyly ectodermal dysplasia cleft syndrome, or EEC, and also referred to as EEC syndrome and split hand split foot ectodermal dysplasia cleft syndrome is
  • defect of dentin formation, and the teeth may be discolored yellow - brown, deep amber or blue - grey with increased translucency. Dentinal dysplasia is another
  • is a condition in which dentin does not form properly and is sometimes associated with osteogenesis imperfecta. Dentin dysplasia is a disorder in which
  • functional odontoblast cells and is likely to function as a regulator of dentin mineralization. FAM20C is a secretory kinase, responsible for the phosphorylation
  • on a tooth root. It is a feature of conditions such as cleidocranial dysplasia and hypophosphatasia. Ireland R 25 March 2010 A Dictionary of Dentistry
  • anodontia MeSH C07.650.800.250 - - - dens in dente MeSH C07.650.800.260 - - - dentin dysplasia MeSH C07.650.800.270 - - - dentinogenesis imperfecta MeSH C07.650.800