Results 11 to 20 of about 2,152 (168)

Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I [PDF]

BMC Genetics, 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
Aiqin Hu, Ting Lu, Danna Chen, Jin Huang, Weiwei Feng, Yanjun Li, Dan Guo, Xiangmin Xu, Dong Chen, Fu Xiong   +9 more
doaj   +2 more sources

Dentin dysplasia type I - A rare entity.

J Oral Maxillofac Pathol, 2015
Dentin dysplasia is a rare disturbance of dentin formation characterized by normal enamel but atypical dentin formation with abnormal pupal morphology. The teeth appear clinically normal in morphologic appearance and color. The teeth characteristically exhibit extreme mobility and are commonly exfoliated prematurely.
Malik S, Gupta S, Wadhwan V, Suhasini GP.   +3 more
europepmc   +4 more sources

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

Molecular Genetics & Genomic Medicine
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.
Yan Wang, Ximin Xu, Yuzhe Ding, Guohua Yuan   +3 more
doaj   +2 more sources

Rootless but Erupted Teeth: Interesting Trait of Dentin Dysplasia Type I [PDF]

Iranian Journal of Orthodontics, 2017
Introduction: Tooth eruption is a complex procedure and many theories has been proposed to describe the nature of this process. Some studies, have shown that in contrast to traditional thoughts, root development is not necessary for tooth eruption and ...
Soodeh Tahmasbi, Sattar Kabiri, Elham Mohammad Rabei   +2 more
doaj   +1 more source

Typical Radiographic Findings of Dentin Dysplasia Type 1b with Dental Fluorosis [PDF]

Case Reports in Dentistry, 2013
S. Venkata Suman, Raviraj Jayam, B. Vijay Kumar, Suresh Dirasantchu, K. Venkata Suneel Kumar, Sameeulla Sk   +5 more
doaj   +2 more sources

Immediate Orthodontic Repositioning of Traumatically Extruded Incisors in a Patient With Cleft Lip and Alveolus: A Case Report. [PDF]

Case Rep Dent
This 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.
europepmc   +2 more sources

Optical Coherence Tomography for Detection of Dental Cracks and Vertical Root Fracture: A Scoping Review. [PDF]

Clin Exp Dent Res
ABSTRACT 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, Albittar AY, Shaikh UM, Takriti M, Baysan A.   +4 more
europepmc   +2 more sources

Dentofacial Features in Schimke Immuno-Osseous Dysplasia: From Childhood to Adolescence. [PDF]

Clin Case Rep
ABSTRACT Schimke immune‐osseous dysplasia (SIOD) is a sporadic multi‐system disorder mainly characterized by spondyloepiphyseal dysplasia, immune insufficiency, and renal failure. Little evidence is available regarding the dentofacial features of SIOD.
Sharifinejad A, Parvizi F, Enteghad M, Ghahramani Y.   +3 more
europepmc   +2 more sources

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, O.E. Berezhna, N.V. Yanko, K.A. Lazareva   +3 more
doaj   +1 more source

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, Gopakumar R Nair, Giridhar Naidu   +2 more
doaj   +1 more source