Results 31 to 40 of about 2,474 (180)

Dentinogénesis imperfecta tipo II: Reporte de un caso

Revista de Odontopediatria Latinoamericana, 2021
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, Leonie Lamothe, Paula Drexler, Raúl Casamayou   +3 more
doaj   +1 more source

Full Mouth Rehabilitation of Two Siblings with Dentinogenesis Imperfecta Type II Using Different Treatment Modalities. [PDF]

Int J Environ Res Public Health, 2020
Alrashdi M, Schoener J, Contreras CI, Chen S.   +3 more
europepmc   +3 more sources

Dentinogenesis imperfecta type 3 [PDF]

, 2020
INSERM
openaire   +2 more sources

Dental management of a child with a rare bone disorder: a case report with a six-year follow up

RGO: Revista Gaúcha de Odontologia, 2020
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, Mariana Oliveira GUIMARÃES, Natália Mendes De Matos CARDOSO, Raiane Machado MAIA, Natália Cristina Ruy CARNEIRO, Ana Cristina BORGES-OLIVEIRA   +5 more
doaj   +1 more source

A Novel Mutation in the TRIP11 Gene: Diagnostic Approach from Relatively Common Skeletal Dysplasias to an Extremely Rare Odontochondrodysplasia

JCRPE, 2022
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, Ayca Dilruba Aslanger, Gözde Yeşil, Nursel H. Elçioğlu   +3 more
doaj   +1 more source

A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review

Indian Journal of Dental Research, 2019
Dentinogenesis Imperfecta and dentin dysplasia are genetic oral diseases inherited in a simple autosomal dominant mode, with high penetrance and a low mutation rate.
Nikita Gulati, Saurabh Juneja, Akriti Singh, Iqbal Singh   +3 more
doaj   +1 more source

Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities. [PDF]

PLoS ONE, 2012
Inherited dentin defects are classified into three types of dentinogenesis imperfecta (DGI) and two types of dentin dysplasia (DD). The genetic etiology of DD-I is unknown.
Shih-Kai Wang, Hui-Chen Chan, Igor Makovey, James P Simmer, Jan C-C Hu   +4 more
doaj   +1 more source

Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families. [PDF]

Mol Genet Genomic Med, 2018
Taleb K, Lauridsen E, Daugaard-Jensen J, Nieminen P, Kreiborg S.   +4 more
europepmc   +3 more sources

Sequentially Functional And Asthetic Restoration Of Severe Dentin Dysplasia

International Dental Journal
Introduction: This case report introduced sequentially functional and aesthetic restoration on a patient with dentin dysplasia type II (DD-II) accompanied by severe tooth wear. Case description: An eight-year-old girl with severe tooth wear presented for
Xuemei Liu, Xu Chen
doaj   +1 more source

A Case of Dentinogenesis Imperfecta Treated with Submerged Root Technique [PDF]

Journal of Clinical and Diagnostic Research, 2015
Dentinogenesis imperfecta (DGI), an autosomal dominant trait, is one of the most common hereditary disorders affecting both the formation and mineralization of dentin. Either or both primary and permanent dentition is affected by it.
Ginjupally Uday, Bhanu Chandar, J. Srilakshmi, Tanya Khaitan, B. Balaji Babu   +4 more
doaj   +1 more source