CLINICAL CASE OF DENTINE DYSPLASIA TYPE I
Український стоматологічний альманах, 2021 Developmental dental hard tissues disorders are rarely diagnosed both in children and adults, and their treatment is a problem for dentist. Despite the fact that molecular genetics studies allow to discriminate some dentine disorders, pathogenesis of ...
L.F. Kaskova +3 more
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Immediate Orthodontic Repositioning of Traumatically Extruded Incisors in a Patient With Cleft Lip and Alveolus: A Case Report. [PDF]
Case Rep DentThis case report describes a 15‐year‐old boy born with a cleft lip and alveolus who sustained severe extrusive and lateral luxation trauma to multiple incisors during the final phase of orthodontic treatment. The displacement caused incisal interference and prevented normal jaw closure.
Middeljans I, Kuijpers MAR, Suttorp CM.
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Optical Coherence Tomography for Detection of Dental Cracks and Vertical Root Fracture: A Scoping Review. [PDF]
Clin Exp Dent ResABSTRACT Objectives Vertical root fractures (VRFs) pose significant clinical challenges and may result in tooth loss. Current diagnostic methods, including conventional radiography and CBCT, are challenging to detect VRFs, especially in the early stages. Optical coherence tomography (OCT) has recently been introduced as a non‐invasive imaging technique
Alkhani MM +4 more
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Dentin dysplasia type II: An exclusive report of two cases in siblings
Journal of Indian Academy of Oral Medicine and Radiology, 2017 Dentin dysplasia is a rare autosomal dominant disorder affecting dentin and resulting in early loss of teeth. Although dentin dysplasia type I is reported to have an incidence of 1 in 100,000, dentin dysplasia type II is considered to be an extremely ...
Deepak Daryani +2 more
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Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I. [PDF]
BMC Genet, 2019 Background Vacuolar protein sorting-associated protein 4B (VPS4B) is a member of the ATP enzyme AAA protein family, and is mainly involved in protein degradation and cell membrane fusion. Recently, a dominant mutation in this gene was identified in human
Hu A +9 more
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An unusual variation of radicular dentin dysplasia: A rare case report with review of literature
Indian Journal of Dental Research, 2020 Dentin dysplasia (DD) is a rare autosomal dominant disorder of dentin development, which is generally divided into two types based on the clinical and radiographic appearance of the affected dentinal tissues: Type-I (Radicular DD) and Type-II (Coronal DD)
Arun K Patnana +2 more
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Dentin dysplasia type 1d: A rare case
Indian Journal of Dental Research, 2014 Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by a defective dentin development with clinically normal-appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts.
Sujit Ranjan Sahoo, Sonia Aggarwal
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Typical radiographic findings of dentin dysplasia type 1b with dental fluorosis. [PDF]
Case Rep Dent, 2013 Suman SV +5 more
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Odontoameloblastoma with extensive chondroid matrix deposition in a guinea pig [PDF]
, 2018 Odontoameloblastomas (previously incorporated within ameloblastic odontomas) are matrix-producing odontogenic mixed tumors and are closely related in histologic appearance to the 2 other types of matrix-producing odontogenic mixed tumors: odontomas and ...
Hedley, J +4 more
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Amyloid-mediated remineralization for tooth hypoplasia of cleidocranial dysplasia
Frontiers in Cellular and Infection Microbiology, 2023 IntroductionCleidocranial dysplasia (CCD) is an autosomal-dominant, heritable skeletal and dental disease, involving hypoplastic clavicles, defective ossification of the anterior fontanelle, dentin and enamel hypoplasia, and supernumerary teeth, which ...
Xiaohe Guo +8 more
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