Results 1 to 10 of about 508 (131)
Amelogenesis Imperfecta; Genes, Proteins, and Pathways
Frontiers in Physiology, 2017 Amelogenesis imperfecta (AI) is the name given to a heterogeneous group of conditions characterized by inherited developmental enamel defects. AI enamel is abnormally thin, soft, fragile, pitted and/or badly discolored, with poor function and aesthetics,
Claire E L Smith +2 more
exaly +3 more sources
THE EFFECT OF AMOXICILLIN ON THE SECRETORY STAGE OF AMELOGENESIS IN RATS [PDF]
Alexandria Dental Journal, 2020 Introduction: Molar–incisor hypomineralization is a developmental enamel defect affecting first permanent molars and incisors. The intake of antibiotics during pregnancy and early childhood has been associated with molar incisor hypomineralization ...
Khadiga Kawana +3 more
doaj +1 more source
Orphanet Journal of Rare Diseases, 2007 Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.
Crawford, Peter +2 more
openaire +3 more sources
Deciphering the functions of Stromal Interaction Molecule-1 in amelogenesis using AmelX-iCre mice
Frontiers in Physiology, 2023 Introduction: The intracellular Ca2+ sensor stromal interaction molecule 1 (STIM1) is thought to play a critical role in enamel development, as its mutations cause Amelogenesis Imperfecta (AI).
Raed Said +10 more
doaj +1 more source
Enamel Defects Associated With Dentin Sialophosphoprotein Mutation in Mice
Frontiers in Physiology, 2021 Dentin sialophosphoprotein (DSPP) is an extracellular matrix protein that is highly expressed in odontoblasts, but only transiently expressed in presecretory ameloblasts during tooth development. We previously generated a knockin mouse model expressing a
Tian Liang +6 more
doaj +1 more source
Journal of Education, Health and Sport, 2022 Introduction: Dental fluorosis is a disease caused by excessive consumption of fluoride and its deposition in the enamel during odontogenesis. The result of this process is the appearance on the surface of permanent teeth of unsightly stains of various ...
Anna Luchowska +2 more
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
Amelogenesis imperfecta. Case report
Revista Científica Odontológica, 2023 The main origin of amelogenesis imperfecta (AI) is a genetic alteration inherited by a family member which affects the dental enamel of the teeth of a person with this condition in various ways. The present clinical case from the Teaching Dental Clinic of the Peruvian University Cayetano Heredia is of a 6-year 5-month-old male child who came to the ...
Nicole Alessandra Herrera-Rojas +1 more
openaire +3 more sources
Amelogenesis imperfecta: an introduction [PDF]
British Dental Journal, 2012 Amelogenesis imperfecta (AI) is an inherited disorder that is associated with mutations in five genes (AMEL; ENAM; MMP20; KLK4 and FAM83H) with a wide range of clinical presentations (phenotypes). It affects the structure and appearance of enamel of all teeth, both in the primary and secondary dentition.
K, Gadhia +3 more
openaire +2 more sources
PENATALAKSANAAN AMELOGENESIS IMPERFEKTA: LAPORAN KASUS
Cakradonya Dental Journal, 2018 Amelogenesis imperfekta (AI) adalah penyakit keturunan berupa gangguan pembentukan email gigi tanpa adanya manifestasi sistemik. Amelogenesis imperfekta dapat terjadi pada gigi sulung maupun gigi permanen.
Elin Hertiana
doaj +1 more source