Results 21 to 30 of about 15,096 (194)
A Novel FAM83H Truncation Mutation Disrupts Enamel Mineralization in Autosomal Dominant Hypocalcified Amelogenesis Imperfecta. [PDF]
Clin Exp Dent ResABSTRACT Objectives Autosomal dominant hypocalcified amelogenesis imperfecta (ADHCAI; OMIM#130900) is a hereditary enamel defect caused by truncation mutations in FAM83H, though the underlying pathogenic mechanisms remain incompletely understood. This study aimed to identify novel FAM83H mutations in a Chinese family with ADHCAI and to investigate ...
Wang Y, Chen H, Lai J, Huang X, Huang Y.
europepmc +2 more sources
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
core +1 more source
Amelogenesis Imperfecta: Direct Restorations Using Injected Composite and Thermoformed Trays
International audienceBackground: Amelogenesis imperfecta is a rare disease (occurring in 1/700 to 1/14000 individuals - ORPHA:88661), and its management often remains a significant challenge for pediatric dentists.
Bouillaud, Inès +3 more
core +9 more sources
Amelogenesis imperfecta: Hypoplastische Form [PDF]
, 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
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
Surgical Pathology Report: Amelogenesis imperfecta
, 2022 Surgical Pathology Report of amelogenesis imperfecta ...
A A A S Adikari (13154171) +1 more
core +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
doaj +1 more source
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
doaj +1 more source