Results 81 to 90 of about 4,274 (211)

Epidemiological and Clinical Features of Regional Odontodysplasia in South Korean Pediatric Patients: A Multicenter Case Series Study

open access: yesInternational Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 140-152, January 2026.
ABSTRACT Background Regional odontodysplasia (RO) is a rare developmental dental anomaly with unknown prevalence. Current knowledge is largely limited to individual case reports. Aim This study aims to present epidemiological data, clinical features, and radiographic characteristics of pediatric and adolescent patients with RO in South Korea. Design In
So Dam Lee   +5 more
wiley   +1 more source

A Novel Variant in Dentin Sialophosphoprotein (DSPP) Gene Causes Dentinogenesis Imperfecta Type III: Case Report. [PDF]

open access: yesMol Genet Genomic Med
Background Hereditary dentin defects are a group of autosomal dominant disorders characterized by developmental abnormalities in dentin formation and mineralization. They can be categorized into dentin dysplasia and dentinogenesis imperfecta.
Wang Y, Xu X, Ding Y, Yuan G.
europepmc   +2 more sources

Relationships between protein and mineral during enamel development in normal and genetically altered mice [PDF]

open access: yes, 2011
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90093/1/EOS_871_sm_SupportingInformation.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/90093/2/j.1600-0722.2011.00871.x ...
Bartlett, John D.   +5 more
core   +1 more source

Evaluation of the Radiographic Features of Idiopathic Osteosclerosis With Cone Beam Computed Tomography (CBCT): A Case Series Study

open access: yesCase Reports in Dentistry, Volume 2026, Issue 1, 2026.
Idiopathic osteosclerosis (IO) is identified by the presence of dense calcified tissue without bone marrow, typically a lack of inflammatory cell infiltration, and having uncertain etiology. This condition is commonly present in the back part of the lower jaw, specifically near the first premolar or molar.
Maryam Mohebiniya   +3 more
wiley   +1 more source

The Bio-Molecular Dynamics of Dental Pulp in Different Clinical Scenarios [PDF]

open access: yes, 2015
Dental pulp (DP) is a very dynamic tissue both in health and in disease. When exposed to stressors and pathological conditions. It undergoes a complex series of biological reactions whereby alterations affect the pulp tissue at tissue cellular and ...
BONAVENTURA, Giuseppe   +3 more
core  

Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation [PDF]

open access: yes, 2016
BACKGROUND: Odonto-onycho-dermal dysplasia (OODD) is a rare form of ectodermal dysplasia characterized by severe oligodontia, onychodysplasia, palmoplantar hyperkeratosis, dry skin, hypotrichosis, and hyperhidrosis of the palms and soles.
Bygum, Anette   +4 more
core   +2 more sources

Current Landscape of Short‐T2 Imaging Techniques in the Musculoskeletal System: The Past, Present and Future

open access: yesJournal of Magnetic Resonance Imaging, Volume 62, Issue 4, Page 969-985, October 2025.
ABSTRACT Conventional MRI is limited in imaging tissues with short T2 relaxation times, such as bone, ligaments, and cartilage, due to their rapid signal decay. This limitation has spurred the development of specialized MRI techniques designed specifically for short‐T2 tissue imaging.
Pranjal Rai   +3 more
wiley   +1 more source

Pulp Stone Formation Following Fixed Orthodontic Treatment: A Panoramic Radiographic Comparison of Extraction and Non‐Extraction Approaches

open access: yesClinical and Experimental Dental Research, Volume 11, Issue 4, August 2025.
ABSTRACT Objective The impact of orthodontic forces on pulp stone formation has been the focus of several studies. Given that orthodontic extractions typically involve the application of greater forces to the teeth, the aim of this study was to compare the extent of pulp stone formation in the molar teeth of patients undergoing orthodontic treatment ...
Kosar Gholinezhad   +4 more
wiley   +1 more source

A rare condition affecting the primary and permanent dentition: Dentin dysplasia type I

open access: yesJournal of Oral and Maxillofacial Radiology, 2013
Dentin dysplasia type I is a genetic defect of dentin formation, which is inherited as an autosomal dominant trait. In this anomaly, the teeth generally appear unremarkable with normal crowns; and it is characterized by normal appearing crowns, absence ...
Ahmet Ercan Sekerci   +4 more
doaj  

Restorative treatment in a case of amelogenesis imperfecta and 9-year follow-up: a case report

open access: yesHead & Face Medicine, 2020
Background Amelogenesis imperfecta is a hereditary malformation showing various manifestations regarding enamel dysplasia. This case report shows a 9-year follow-up after restorative treatment of a 16-year old female patient affected by a hypoplastic ...
Martin M. I. Sabandal   +2 more
doaj   +1 more source

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