Results 31 to 40 of about 4,451 (219)
Rehabilitation of an attrited dentition is one of the most challenging task faced by a prosthodontist which requires a systematic, phase wise approach. Hobo’s techniques and Pankey Mann Schuyler’s philosophy are widely used and documented for full mouth ...
Amina +4 more
doaj +2 more sources
Dentinogenesis imperfecta type II dentin: nanostructural mechanics analysis [PDF]
Jia G +10 more
europepmc +3 more sources
Full Mouth Rehabilitation of Two Siblings with Dentinogenesis Imperfecta Type II Using Different Treatment Modalities. [PDF]
Alrashdi M +3 more
europepmc +3 more sources
Personalized Bonding Approach for Full‐Mouth Adhesive Rehabilitation in Dentinogenesis Imperfecta [PDF]
ABSTRACT Dentinogenesis imperfecta is a rare genetic disorder impacting dentin structure, with an incidence of 1 in 6000 to 1 in 8000 individuals. This condition alters the tooth's color and structure, affecting patients aesthetically, functionally, and socially.
Clark C, Kérourédan O, Massé L.
europepmc +2 more sources
Dentinogénesis imperfecta tipo II: Reporte de un caso
La Dentinogénesis Imperfecta es un desorden genético de carácter hereditario autosómico dominante, que se caracteriza por defectos en la dentina de ambas denticiones.
Magdalena San Martín +3 more
doaj +1 more source
A cephalometric method to diagnosis the craniovertebral junction abnormalities in osteogenesis imperfecta patients [PDF]
Osteogenesis imperfecta (OI) is a hereditary bone fragility disorder that in most patients is caused by mutations affecting collagen type I. Their typical oral and craneofacial characteristics (Dentinogenesis imperfecta type I and class III malocclusion),
de Nova García, Joaquín +6 more
core +4 more sources
Dental management of a child with a rare bone disorder: a case report with a six-year follow up
Osteogenesis imperfecta is a rare genetic disorder involving abnormal type I collagen composition that compromises bone and collagen-rich tissues. Individuals with Osteogenesis imperfecta exhibit oral and systemic abnormalities, including dentinogenesis ...
Suélen Alves TEIXEIRA +5 more
doaj +1 more source
Odontochondrodysplasia (ODCD, OMIM #184260) is a rare, non-lethal skeletal dysplasia characterized by involvement of the spine and metaphyseal regions of the long bones, pulmonary hypoplasia, short stature, joint hypermobility, and dentinogenesis ...
Burcu Yeter +3 more
doaj +1 more source
Minimally invasive orthodontics: elastodontic therapy in a growing patient affected by Dentinogenesis Imperfecta [PDF]
AIM: The aim of the study was to report the use of an elastodontic therapy in a growing patient affected by Dentinogenesis Imperfecta, second class malocclusion, deep bite and lower arch crowding from the deciduous dentition to permanent one. CASE
IERARDO, GAETANO +4 more
core +1 more source

