Results 31 to 40 of about 4,008 (210)

A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review

Indian Journal of Dental Research, 2019
Dentinogenesis Imperfecta and dentin dysplasia are genetic oral diseases inherited in a simple autosomal dominant mode, with high penetrance and a low mutation rate.
Nikita Gulati, Saurabh Juneja, Akriti Singh, Iqbal Singh   +3 more
doaj   +1 more source

Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities. [PDF]

PLoS ONE, 2012
Inherited dentin defects are classified into three types of dentinogenesis imperfecta (DGI) and two types of dentin dysplasia (DD). The genetic etiology of DD-I is unknown.
Shih-Kai Wang, Hui-Chen Chan, Igor Makovey, James P Simmer, Jan C-C Hu   +4 more
doaj   +1 more source

Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families [PDF]

, 2011
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90129/1/EOS_874_sm_FigS1-9.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/90129/2/j.1600-0722.2011.00874.x ...
Bai, Barron, Beattie, Begue-Kirn, Bhuvanagiri, Bleyer, Bronckers, Choo, Duffaud, Hart, Holappa, Hon, Hughes, Jonsson, Kawasaki, Kawasaki, Kida, Kim, Kim, Kim, Kutz, Lee, Lee, Lee, Lee, Lee, Malmgren, McKnight, McKnight, Meredith, Nagano, Nanci, Nieminen, Paetzel, Rajpar, Simmer, Song, Song, Sreenath, Sun, Suzuki, Tsuchiya, Tsukumo, Vijayasarathy, Von Marschall, Wang, Wright, Xiao, Yamakoshi, Yamakoshi, Zhang, Zhang   +51 more
core   +1 more source

Isolated olecranon fractures in children affected by osteogenesis imperfecta type I treated with single screw or tension band wiring system: outcomes and pitfalls in relation to bone mineral density [PDF]

, 2017
The purpose of this study is to compare the results of 2 techniques, tension band wiring (TBW) and fixation with screws, in olecranon fractures in children affected with osteogenesis imperfecta (OI) type I.
D'Eufemia, Patrizia, De Cristo, Claudia, Graci, Jole, Martini, Lorena, Persiani, Pietro, Ranaldi, Filippo M., Villani, Ciro, Zambrano, Anna   +7 more
core   +1 more source

Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome [PDF]

, 2013
Background: Whereas mutations affecting the helical domain of type I procollagen classically cause Osteogenesis Imperfecta (OI), helical mutations near the amino (N)-proteinase cleavage site have been suggested to result in a mixed OI/Ehlers-Danlos ...
De Paepe, Anne, Goemans, Nathalie, Gyftodimou, Yolanda, Holmberg, Eva, Lopez-Gonzalez, Vanesa, Malfait, Fransiska, Mortier, Geert, Nampoothiri, Sheela, Petersen, Michael Bjorn, Symoens, Sofie   +9 more
core   +4 more sources

The clinical features of osteogenesis imperfecta in Vietnam [PDF]

, 2017
Purpose Osteogenesis imperfecta (OI) has not been studied in a Vietnamese population before. The aim of this study was to systematically collect epidemiological information, investigate clinical features and create a clinical database of OI patients in ...
Bich Ngoc, Can T, Binh, Ho Duy, Dung, Vu Chi, Hung, Ton That, Koks, Sulev, Maasalu, Katre, Martson, Aare, Nam, Tran V, Prans, Ele, Reimann, Ene, Thanh Nhan, Le N, Zhytnik, Lidiia   +11 more
core   +1 more source

Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia [PDF]

, 2016
Dental anomalies are not an unusual finding in routine dental examination. The effect of dental anomalies can lead to functional, esthetic and occlusal problems.
Yassin, Syed M.
core   +1 more source

Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations [PDF]

, 2015
Background: Raine syndrome (RS) is a rare autosomal recessive bone dysplasia typified by osteosclerosis and dysmorphic facies due to FAM20C mutations. Initially reported as lethal in infancy, survival is possible into adulthood. We describe the molecular
A Linde, A Rejjal, AE Kan, Alan J Mighell, Ana Carolina Acevedo, AX Acosta, C Chaussain-Miller, C Gaucher, Caroline Lourenço de Lima, Chris F Inglehearn, Claire E L Smith, Clare V Logan, CM Giachelli, Colin A Johnson, D Chitayat, D Nalbant, David A Parry, E Katchburian, FK Ababneh, G Hulskamp, G Jaureguiberry, GS Kochar, HM Kingston, HO Ishikawa, J Dong, J Hao, J Raine, James A Poulter, K Al-Mane, KA Al Mane, L Ye, LI Al-Gazali, Lilian M Paula, Luiz Claudio Castro, LW Fisher, M Dure-Molla de la, M Fradin, M Koob, MA DePristo, MA Simpson, MA Simpson, P Vogel, Paulo Marcio Yamaguti, PJ Patel, Priscila Gomes Alves, PS Hart, S Takeyari, SA Shalev, SH Rafaelsen, SK Wang, SK Wang, SM Hebsgaard, T Gunes, T Mahafza, T Sreenath, V Faundes, VS Tagliabracci, X Wang, X Wang, X Wang, X Wang, Y Kinoshita   +61 more
core   +2 more sources

Sequentially Functional And Asthetic Restoration Of Severe Dentin Dysplasia

International Dental Journal
Introduction: This case report introduced sequentially functional and aesthetic restoration on a patient with dentin dysplasia type II (DD-II) accompanied by severe tooth wear. Case description: An eight-year-old girl with severe tooth wear presented for
Xuemei Liu, Xu Chen
doaj   +1 more source

A Case of Dentinogenesis Imperfecta Treated with Submerged Root Technique [PDF]

Journal of Clinical and Diagnostic Research, 2015
Dentinogenesis imperfecta (DGI), an autosomal dominant trait, is one of the most common hereditary disorders affecting both the formation and mineralization of dentin. Either or both primary and permanent dentition is affected by it.
Ginjupally Uday, Bhanu Chandar, J. Srilakshmi, Tanya Khaitan, B. Balaji Babu   +4 more
doaj   +1 more source