Dental Anomalies Part II Flashcards
what is amelogenesis imperfecta
- inherited genetic mutation
- isolate or syndromicc
- enamel is affected in all or nearly all teeth
what dentition is affected in amelogenesis imperfecta
primary and permanent
what is type 1 alemogenesis imperfecta
hypoplastic type: thinner but hard enamel
what is type 2 amelogenesis imperfecta
hypomaturation type: relatively hard but colored (not translucent)
what is type III amelogenesis imperfecta
hypomineralized or hypocalcified: softer rough colored undermineralized enamel
what is type IV amelogenesis imperfecta
hypoplastic- hypomature with taurodontism
describe the type 1 hypoplastic type amelogenesis imperfecta
- thin bur mineralized enamel. looks radiopaque
- quantitative enamel defect: failure during enamel matrix secretory stage (enamel agenesia is rare)
- generalized or localized, pits, striae, groove defects
- diffuse smooth or rough
- teeth appear white to yellow-brown, small, and square shaped
- open contacts “picket fence” appearance. flat occlusal surface, low cusps
- delayed eruption and increased impaction
describe type II amelogenesis imperfecta
- normal thickness of enamel. a qualitative defect
- soft enamel - as radiodense as dentin
- less translucid enamel: cloudy white, yellow or brown color
- hard and protective
describe type III amelogenesis imperfecta
- enamel of normal thickness but soft, porous and shedding easily from the dentin. normal shape at eruption
- these teeth are very sensitive even to physical contact with a toothbrush
- soft enamel that is less dense than dentin in radiographs
- grossly worn teeth to gingival level
- the color of enamel can range from white to creamy yellow-brown
describe dentinogenesis imperfecta
- primary dentition more severely affected
- amberlike translucency (yellow to blue-gray)
- enamel separates easily from dentin (faulty DEJ)
- accelerated attrition -> anterior open bite
- cervical constriction -> bulbous crown
- short and slender roots
- partial or complete obliteration of pulp chambers and canals
- types I, II and III
describe type I dentinogenesis imperfecta
- associated with osteogenesis imperfecta
- mutation in collagen synthesis genes
describe type II dentinogenesis imperfecta
- no skeletal defects
- enlarged pulp chambers in primary teeth (occasional)d
describe type III dentinogenesis imperfecta
- brandywine isolate
- found in people originating from southern maryland
- enlarged pulp chambers
- pulp exposure
what are the acquired abnormalities
- attrition
- abrasion
- erosion
- third molar impaction
what is attrition
physiologic wear of teeth