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A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues. [PDF]
Wang SK, Lee ZH, Aref P, Chu KY.
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Trichodysplasia and amelogenesis imperfecta
Oral Surgery, Oral Medicine, Oral Pathology, 1993This paper describes a family in which members of two generations have an X-linked type of enamel dysplasia. All affected persons have symmetric pits in the cuticles of their hair shafts. The observation of these concurrent traits raises questions about the classification of amelogenesis imperfecta and the value of microscopic studies of the hair in ...
G, Angelos, R J, Jorgenson
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Amelogenesis Imperfecta: Case Study
Operative Dentistry, 2017SUMMARY Amelogenesis imperfecta (AI) refers to a group of rare genetic disorders that involve tooth development and that are passed down through families as a dominant trait. This condition is characterized by abnormal enamel formation caused by gene mutations that alter the quality and/or quantity of enamel.
C, Leevailoj +2 more
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Multidisciplinary treatment of amelogenesis imperfecta
Nederlands Tijdschrift voor Tandheelkunde, 2021A healthy 13-year-old patient with amelogenesis imperfecta was referred by her orthodontist to the joint consultation hour (Center for Specialised Dentistry and Oral and Maxillofacial Surgery). In addition to her amelogenesis imperfecta, she was diagnosed with a class 2 malocclusion and a mandibular hypoplasia.
G, Mensink +3 more
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Amelogenesis imperfecta with taurodontism
Oral Surgery, Oral Medicine, Oral Pathology, 1979Reports of families having a combination of amelogenesis imperfecta and taurodontism are limited. This study of members of three families shows that the combination is inherited as an autosomal dominant trait. In each of the patients examined, neither condition was seen without the other.
J, Congleton, E J, Burkes
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Amelogenesis imperfecta in cattle
Veterinary Record, 2011PATHOLOGICAL conditions of the teeth are infrequently reported, particularly in cattle ([Brown and others 2007][1], [Radostits and others 2007][2]). These include malocclusion, porphyrinuria, and complex skeletal diseases such as osteogenesis imperfecta, dental fluorosis and enamel erosion ...
M P, Cranwell, A, Schock
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Ultrastructural study of amelogenesis imperfecta
Calcified Tissue Research, 1977An ultrastructural study of teeth with amelogenesis imperfecta revealed various aspects of microcavities in the enamel surface, which ranged from isolated imprints of ameloblasts corresponding to the mildest lesions at the end of amelogenesis, to pits caused by the death of 20 to 30 ameloblasts at the beginning of amelogenesis.
B, Kerebel, G, Daculsi
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Microradiographic study of amelogenesis imperfecta
European Journal of Oral Sciences, 1989Abstract – A material of 22 primary and 4 permanent teeth from 22 children with amelogenesis imperfecta (AI) were examined by microradiographic techniques. The children were part of a patient material earlier examined in genetical and clinical studies.
B, Bäckman, G, Anneroth
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