Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children [PDF]
Dentistry 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.
Huong Thi Thu Nguyen +6 more
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Regenerative Endodontic Treatment in Dentinogenesis Imperfecta-Induced Apical Periodontitis [PDF]
Case Reports in DentistryPulp 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
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Dentinogenesis imperfecta in a 6-year-old male neutered Labrador retriever: Case report with atypical clinical presentation and treatment review [PDF]
Frontiers in Veterinary ScienceThis case report details the diagnosis and treatment of dentinogenesis imperfecta in a 6-year-old neutered male Labrador, presenting without concurrent osteogenesis imperfecta.
Karolina Maria Piekos +4 more
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Personalized Bonding Approach for Full-Mouth Adhesive Rehabilitation in Dentinogenesis Imperfecta. [PDF]
Clin Case RepABSTRACT 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.
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Osteogenesis imperfecta and dentinogenesis imperfecta: Clinical features and dental management
Current 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
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Prosthodontic rehabilitation of dentinogenesis imperfecta
Contemporary 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
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Splicing mutation in DSPP causes dentinogenesis imperfecta and amelogenesis imperfecta [PDF]
BMC Oral HealthBackground Dentin sialophosphoprotein (DSPP) is an extracellular matrix protein, which is highly expressed in odontoblasts and transiently expressed in presecretory ameloblasts.
Zhenwei Zhang +7 more
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Dentinogenesis imperfecta: A case report
Journal 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
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Dentinogenesis imperfecta associated with osteogenesis imperfecta
Dental 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
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Management of Osteogenesis Imperfecta Complicated by Severe Pneumonia in a Resource-Limited Setting: A Case Report. [PDF]
Case Rep PediatrIntroduction Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility, skeletal deformities, and multisystem involvement, with respiratory complications representing a major cause of morbidity and mortality. Intrinsic pulmonary abnormalities, restrictive physiology from scoliosis, and impaired secretion clearance increase
Shah BK +6 more
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