Results 1 to 10 of about 4,274 (211)

Rootless teeth: Dentin dysplasia type I.

Contemp Clin Dent, 2013
A rare case of hereditary disturbance of dentine, Dentin dysplasia type I is presented, which is characterized by short or total absence of roots, obliterated pulp chambers, and peri-apical radiolucencies. It affects both primary and secondary dentition.
Fulari SG, Tambake DP.
europepmc   +5 more sources

Dentin dysplasia type I: a case report and review of the literature [PDF]

Journal of Medical Case Reports, 2010
Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts ...
Lida Toomarian, Fatemeh Mashhadiabbas, Mahkameh Mirkarimi, Leili Mehrdad, JW Kim, G Ballschmiede, MA Rushton, Jr Witkop CJ, B Neville, JA Regezi, J Logan, RK Wesley, T Perl, ME Morris, RP Elzay, L Ozer, SH Ravanshad, G Ansari, MF Muñoz-Guerra   +18 more
core   +3 more sources

Dentin dysplasia: diagnostic challenges. [PDF]

BMJ Case Rep, 2018
Dentin dysplasia(DD) is a rare autosomal dominant disorder associated with disturbance of the dentin. While the crowns appear clinically normal, on radiography, the pulp spaces appear partially or completely obliterated, with short blunted roots, and multiple periapical radiolucencies affecting the apparently sound teeth.
Alhilou A, Beddis HP, Mighell AJ, Durey K.   +3 more
europepmc   +4 more sources

Dentin dysplasia type I. [PDF]

BMJ Case Rep, 2013
Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterised clinically by nearly normal appearing crowns and hypermobility of teeth that affects one in every 100 000 individuals and manifests in both primary and permanent dentitions.
Singh A, Gupta S, Yuwanati MB, Mhaske S.
europepmc   +4 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

Recent Advances and the Potential for Clinical Use of Autofluorescence Detection of Extra-Ophthalmic Tissues [PDF]

, 2020
The autofluorescence (AF) characteristics of endogenous fluorophores allow the label-free assessment and visualization of cells and tissues of the human body.
Aigner, Felix, Pratschke, Johann, Schumann, Teresa, Stockmann, Martin, Tacke, Frank, Theil, Donna, Wizenty, Jonas, Wuensch, Tilo   +7 more
core   +1 more source

Meeting report: a hard look at the state of enamel research. [PDF]

, 2017
The Encouraging Novel Amelogenesis Models and Ex vivo cell Lines (ENAMEL) Development workshop was held on 23 June 2017 at the Bethesda headquarters of the National Institute of Dental and Craniofacial Research (NIDCR).
Bartlett, John D, DenBesten, Pamela, Diekwisch, Thomas Gh, Duverger, Olivier, Joester, Derk, Klein, Ophir D, Kulkarni, Ashok B, Lacruz, Rodrigo S, Millar, Sarah E, Moradian-Oldak, Janet, Pugach, Megan K, Shaw, Wendy, Simmer, James P, Wright, J Timothy   +13 more
core   +1 more source

Minimally invasive orthodontics: elastodontic therapy in a growing patient affected by Dentinogenesis Imperfecta [PDF]

, 2017
AIM: The aim of the study was to report the use of an elastodontic therapy in a growing patient affected by Dentinogenesis Imperfecta, second class malocclusion, deep bite and lower arch crowding from the deciduous dentition to permanent one. CASE
IERARDO, GAETANO, LUZZI, Valeria, NARDACCI, GIULIANA, POLIMENI, Antonella, VOZZA, Iole   +4 more
core   +1 more source

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia [PDF]

Orphanet Journal of Rare Diseases, 2008
Abstract The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000,
Barron, Martin J., McDonnell, Sinead T., MacKie, Iain, Dixon, Michael J.   +3 more
openaire   +4 more sources

Double talon cusps on supernumerary tooth fused to maxillary central incisor: review of literature and report of case [PDF]

, 2014
Human tooth development is a continuous process begin at the sixth weeks in utero and extends to about sixth months after birth for the primary dentition and from sixteenth week in utero to late adolescence for permanent dentition.
Hattab, Faiez N.
core   +4 more sources