Results 21 to 30 of about 3,804 (207)
Molar incisor hypomineralisation: current knowledge and practice
International Dental Journal, EarlyView., 2020 Background Molar incisor hypomineralisation (MIH) is a common developmental dental condition that presents in childhood. Areas of poorly formed enamel affect one or more first permanent molars and can cause opacities on the anterior teeth. MIH presents a variety of challenges for the dental team as well as functional and social impacts for affected ...
Helen D. Rodd +4 more
wiley +1 more source
Treatment plan: Amelogenesis Imperfecta
, 2022 The treatment plan of a patient diagnosed with amelogenesis ...
A A A S Adikari (13154171) +1 more
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Surgical Pathology Report: Amelogenesis imperfecta
, 2022 Surgical Pathology Report of amelogenesis imperfecta ...
A A A S Adikari (13154171) +1 more
core +1 more source
Frontiers in Genetics, 2022 Amelogenesis imperfecta is a congenital disorder within a heterogeneous group of conditions characterized by enamel hypoplasia. Patients suffer from early tooth loss, social embarrassment, eating difficulties, and pain due to an abnormally thin, soft ...
Akiko Suzuki +15 more
doaj +1 more source
Enamel renal syndrome: A rare case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2012 Enamel renal syndrome is a very rare disorder associating amelogenesis imperfecta with nephrocalcinosis. It is known by various synonyms such as amelogenesis imperfecta nephrocalcinosis syndrome, MacGibbon syndrome, Lubinsky syndrome, and Lubinsky ...
S V Kala Vani, M Varsha, Y Uday Sankar
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Prosthodontic rehabilitation: Cutting edge treatment for amelogenesis imperfecta
Indian Journal of Dental Sciences, 2022 Amelogenesis imperfecta is a genetically determined inherited disorder characterized by abnormal formation of tooth enamel leading to esthetic, functional, and psychological impact on the patient.
Saurav Banerjee, Debabrata Biswas
doaj +1 more source
Molecular Basis of Human Enamel Defects
Balkan Journal of Dental Medicine, 2014 During eruption of teeth in the oral cavity, the effect of gene variations and environmental factors can result in morphological and structural changes in teeth.
Chatzopoulos Georgios, Tziafas Dimitrios
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Journal of Craniomaxillofacial Research, 2020 Introduction: Tooth enamel is a precious and highly mineralized tissue in the human body. Amelogenesis Imperfecta (AI) is a developmental, evolutionary and hereditary disease presents with the rare abnormal formation of enamel that affects the primary ...
Shamsoulmolouk Najafi +4 more
doaj +1 more source
Amelogenesis imperfecta in the dentition of a wild chimpanzee. [PDF]
, 2017 This report describes a case of amelogenesis imperfecta in the dentition of a female chimpanzee. Amelogenesis imperfecta is a group of rare genetic conditions that create severe enamel defects, which, although well researched in humans, has not yet been ...
Irish, JD +8 more
core +1 more source
Amelogenesis imperfecta: Hypoplastische Form
, 2016 Amelogenesis imperfecta (AI) is a hereditary enamel development disorder that is not associated with an underlying systemic disease. The prevalence varies between 1:20,000 and 1:718 depending on the population.Amelogenesis imperfecta (AI) is a hereditary
Ramseyer, Simon, Lussi, Adrian
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