Results 1 to 10 of about 2,117 (162)

Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children [PDF]

open access: yesDentistry Journal, 2021
Osteogenesis imperfecta (OI) is a genetic disorder characterized by increased bone fragility and low bone mass, caused mainly by mutations in collagen type I encoding genes.
Van Khanh Tran   +2 more
exaly   +4 more sources

Dentinogenesis imperfecta in a 6-year-old male neutered Labrador retriever: Case report with atypical clinical presentation and treatment review [PDF]

open access: yesFrontiers in Veterinary Science
This case report details the diagnosis and treatment of dentinogenesis imperfecta in a 6-year-old neutered male Labrador, presenting without concurrent osteogenesis imperfecta.
Cynthia Bell
exaly   +4 more sources

Dentinogenesis Imperfecta in Primary Dentition: Case Report [PDF]

open access: yesReports
Background and Clinical Significance: Dentinogenesis imperfecta is a hereditary dentin disorder that compromises tooth structure, esthetics, and function.
Līna Petrova   +2 more
doaj   +2 more sources

Regenerative Endodontic Treatment in Dentinogenesis Imperfecta-Induced Apical Periodontitis [PDF]

open access: yesCase Reports in Dentistry
Pulp involvement of immature permanent teeth with dentinogenesis imperfecta is challenging and could lead to extraction. A case of dentinogenesis imperfecta-induced periapical periodontitis of an immature permanent tooth was treated with regenerative ...
Ying Liao, Ting Pan, Xianghui Xing
doaj   +2 more sources

Dentinogenesis imperfecta associated with osteogenesis imperfecta

open access: yesDental Research Journal, 2012
This paper presents a case with dentinogenesis imperfecta (DI) associated with osteogenesis imperfecta. Systemic and dental manifestations of OI and its medical and dental treatments are discussed in this paper.
Mina Biria   +3 more
doaj   +3 more sources

Osteogenesis imperfecta and dentinogenesis imperfecta: Clinical features and dental management

open access: yesCurrent Medicine Research and Practice, 2022
Osteogenesis imperfecta (OI) is a rare congenital condition, marked by fragile bones, skeletal deformities and additional extra-skeletal symptoms. Depending upon the degree of seriousness, affected people can either carry on with a mostly unrestricted ...
Chetna Grover   +3 more
doaj   +2 more sources

Prosthodontic rehabilitation of dentinogenesis imperfecta

open access: yesContemporary Clinical Dentistry, 2011
Dentinogenesis imperfecta and its prosthodontic management is a challenging task. Treatment protocol varies according to clinical case. Although various reports in the literature suggest general guidelines for treatment planning, the present case report ...
Anil Goud, Saee Deshpande
doaj   +3 more sources

Dentinogenesis imperfecta: A case report

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2008
Dentinogenesis imperfecta is an autosomal dominant disorder of tooth development characterized by the presence of opalescent dentin, resulting in a dusky blue to brownish discoloration of the teeth.
Subramaniam P, Mathew S, Sugnani S
doaj   +3 more sources

Multidisciplinary Oral Rehabilitation in Osteogenesis Imperfecta: 18-Year-Old Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder characterized by bone fragility and Type I collagen defects. Although dentinogenesis imperfecta (DI) is a classic manifestation, patients with OI may experience significant dental deterioration even in its absence due to inherent dentinal weakness.
Mozafari PM   +3 more
europepmc   +2 more sources

Splicing mutation in DSPP causes dentinogenesis imperfecta and amelogenesis imperfecta [PDF]

open access: yesBMC Oral Health
Background Dentin sialophosphoprotein (DSPP) is an extracellular matrix protein, which is highly expressed in odontoblasts and transiently expressed in presecretory ameloblasts.
Zhenwei Zhang   +7 more
doaj   +2 more sources

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