Results 91 to 100 of about 2,550 (192)
Oral rehabilitation of a child with dentinogenesis imperfecta – case report
eport the clinic case of a 5-yearold boy with presenting yellow-gray teeth and generalized severe tooth crown wear. Case report: After clinical and radiographic examination, he was diagnosed with dentinogenesis imperfecta.
Rayen Milanao Drugowick +4 more
core +1 more source
Compromised alveolar bone cells in a patient with dentinogenesis imperfecta caused by DSPP mutation
International audienceDentin sialophosphoprotein (DSPP) plays an important role in the mineralization of both dentin and bones. The Dspp null mice developed periodontal diseases. Patients with DSPP mutations have dentinogenesis imperfecta (DGI), but very
Thantrira Porntaveetus +19 more
core +1 more source
Dental Findings and Treatment in Osteogenesis Imperfecta: A Case Report
Osteogenesis imperfecta (OI) is a genetically inherited disease in which increased bone fragility, low bone mass, and connective tissue disorders are seen. In other words, 'glass bone disease'; has been associated with blue sclera, hearing problems, hand-
Yasemin İspir, Özge Anıl
doaj +1 more source
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 +1 more source
Osteogenesis imperfecta associated with dentinogenesis imperfecta
Objetivo: O presente trabalho tem como objetivo fazer uma revisão da literatura sobre as manifestações orais da Osteogênese Imperfeita. Metodologia: Revisão integrativa da literatura, qualitativa de cunho descritiva e foram utilizadas as bases de dados SciELO - Scientific Eletronic Library Online, a PubMed- National Library of Medicine e a Plataforma ...
Azevedo, Marcelle Jayne Santos +3 more
openaire +1 more source
Osteogenesis imperfecta, a case report
Introduction: osteogenesis imperfecta or crystal bones constitute the hereditary osteoporotic syndrome with the highest incidence in childhood. Case report: a 6-year and three-month-old school student admitted to the pediatric intensive care unit with a
Lázaro Raidel Moreira-Díaz +2 more
doaj
Morphological and Ultrastructural Collagen Defects: Impact and Implications in Dentinogenesis Imperfecta. [PDF]
Gadi LSA, Chau DYS, Parekh S.
europepmc +1 more source
Dentinogenesis imperfecta type II: Ultrastructure of teeth in sagittal sections
The morphological abnormalities of the teeth of patients affected by dentinogenesis imperfecta type 2 (DI-II) may underlie the difficulties with the clinical restoration of such teeth.
Loster, Jolanta; Jagiellonian University, Kraków, Poland +1 more
core +1 more source
Mouse Dspp frameshift model of human dentinogenesis imperfecta. [PDF]
Liang T +11 more
europepmc +1 more source

