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Published in 2018 at "Clinical Oral Investigations"
DOI: 10.1007/s00784-018-2437-7
Abstract: ObjectivesDentin 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 little is known… read more here.
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Published in 2024 at "Clinical Oral Investigations"
DOI: 10.1007/s00784-024-05636-z
Abstract: Dentinogenesis imperfecta (DI) is an inherited dentin defect and may be isolated or associated with disorders such as osteogenesis imperfecta, odontochondrodysplasia Ehler-Danlos and others. Isolated DI is caused mainly by pathogenic variants in DSPP gene… read more here.
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Published in 2020 at "Archives of oral biology"
DOI: 10.1016/j.archoralbio.2020.104815
Abstract: AIM To investigate the chemical and mechanical properties of teeth affected by a 1-bp deletion (c.2688delT) in the DSPP gene. METHODS AND MATERIALS Maxillary first premolars were extracted from the affected individual at age 9… read more here.
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Published in 2021 at "Journal of dentistry"
DOI: 10.1016/j.jdent.2021.103654
Abstract: OBJECTIVES A better understanding of the microstructure and mechanical properties of enamel and dentine may enable practitioners to apply the current adhesive dentistry protocols to clinical cases involving dentine disorders (dentinogenesis imperfecta or dentine dysplasia).… read more here.
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Published in 2024 at "Medicine"
DOI: 10.1097/md.0000000000036882
Abstract: Rationale: Dentinogenesis imperfecta (DI) is an autosomal-dominant disorder. The most common clinical manifestations, including obliterated tooth tissues and severe tooth wear, usually lead to tooth extractions. It remains a great challenge for dentists to preserve… read more here.
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Published in 2023 at "Journal of Dental Research"
DOI: 10.1177/00220345231154569
Abstract: Dentinogenesis imperfecta (DI) is the main orodental manifestation of osteogenesis imperfecta (OI) caused by COL1A1 or COL1A2 heterozygous pathogenic variants. Its prevalence varies according to the studied population. Here, we report the molecular analysis of… read more here.
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Published in 2024 at "Iranian Endodontic Journal"
DOI: 10.22037/iej.v19i4.45902
Abstract: Pulp canal calcification (PCC) is common in patients with dentinogenesis imperfecta (DGI). We present endodontic management of multiple anterior and posterior teeth with PCCs in a patient with DGI type II using guided endodontics. A… read more here.
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Published in 2023 at "Dentistry Journal"
DOI: 10.3390/dj11040095
Abstract: Collagen is the building block for the extracellular matrix in bone, teeth and other fibrous tissues. Osteogenesis imperfecta (OI), or brittle bone disease, is a heritable disorder that results from defective collagen synthesis or metabolism,… read more here.
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Published in 2022 at "Healthcare"
DOI: 10.3390/healthcare10081453
Abstract: Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated with osteogenesis imperfecta (OI). Aim: To describe and study the morphological characteristics of DGI-I with scanning electron microscopy (SEM). Material and methods:… read more here.