Results 81 to 90 of about 6,417 (245)
Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause developmental alterations in the structure of the enamel in the absence of a systemic disorder.
Derya Özdemir Doğan+2 more
doaj +1 more source
Amelogenesis imperfecta, a rare disease, represents inherited, congenital defects that primarily affect enamel with esthetic and functional impairment affecting everyday life.
Salomé Mascarell+3 more
doaj +1 more source
Enamel and dentin mineralization in familial hypophosphatemic rickets: a micro-CT study [PDF]
Objectives: The aim of the present study was to analyse the mineralization pattern of enamel and dentin in patients affected by X-linked hypophosphatemic rickets (XLHR) using micro-CT (µCT), and to associate enamel and dentin mineralization in primary ...
Costa, F. W. G.+4 more
core +1 more source
ABSTRACT Junctional epidermolysis bullosa (JEB) is a rare genodermatosis characterized by fragility of the skin and mucous membranes due to alterations in the dermal epidermal junction. This condition manifests as mechanically induced bullous lesions that heal with hypertrophic granulation tissue and/or atrophic scars.
Marina Goldoni+9 more
wiley +1 more source
Full mouth rehabilitation of a young adult patient with Amelogenesis imperfecta
Amelogenesis imperfecta is a group of hereditary disorder without systemic involvement. Restoration of dentition with this disorder involves both esthetic and functional rehabilitation to improve the psychological status of the patient.
Mahendran Kavitha+2 more
doaj
Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta
Amelogenesis imperfecta is a group of rare inherited disorders that affect tooth enamel formation, quantitatively and/or qualitatively. The aim of this study was to identify the genetic etiologies of two families presenting with hypomaturation ...
Jung-Wook Kim+11 more
doaj +1 more source
Linear enamel hypoplasia (LEH) prevalence in the teeth of Cayo Santiago rhesus monkeys (Macaca mulatta). Defects matched on right and left teeth and the increase in the frequency of LEH by decade. ABSTRACT Linear enamel hypoplasias (LEHs) are development defects appearing as lines or grooves on enamel surfaces.
Debbie Guatelli‐Steinberg+11 more
wiley +1 more source
Molecular and circadian controls of ameloblasts [PDF]
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90102/1/j.1600-0722.2011.00918.x ...
Atanasov+32 more
core +1 more source
Knowledge and management of molar–incisor hypomineralisation amongst dentists in The Netherlands
Abstract Background Molar–incisor hypomineralisation (MIH) is a frequently encountered dental condition in the clinical setting, and correct diagnosis can influence management outcomes. Aim To assess the knowledge of and attitudes towards the management of MIH amongst dentists in the Netherlands.
Foteini Papanikolaou+5 more
wiley +1 more source
Amelogenesis Imperfecta : A Case Report
{"references": ["1.\tMJ Aldred, R Savarirayan, PJM Crawford, Oral Diseases (2003) 9, 19\u201323 2.\tM. Kida, T. Ariga, T. Shirakawa,H. Oguchi, and Y. Sakiyama, Journal of Dental Research 81(11):738-742, 2002 3.\tShafer's Text Book Of Oral Pathology Shafer,Hine 6th Edition. 4.\tOral And Maxillofacial Pathology Neville ,Dam,Allen 3rd Edition.
Thakran, Dinesh, , Ruby, Kumar, Sunil
openaire +2 more sources