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Amelogenesis imperfecta. case report. [PDF]
Rev Cient Odontol (Lima), 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 ...
Herrera-Rojas NA +1 more
europepmc +4 more sources
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 ...
Aldred Michael +2 more
doaj +3 more sources
Full Mouth Rehabilitation with All-Ceramic Restorations in a Patient with Amelogenesis Imperfecta: A Case Report with 10-Year Follow-Up [PDF]
Dentistry JournalBackground: Amelogenesis imperfecta (AI) includes a group of inherited disorders that affect enamel formation, both in quality and quantity. It may cause anomalies in a number of teeth or a group of teeth, or it may be present in the whole dentition. The
Stefanos Kourtis
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Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta [PDF]
Frontiers in Physiology, 2017 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
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Restorative treatment in a case of amelogenesis imperfecta and 9-year follow-up: a case report [PDF]
Head & Face Medicine, 2020 Background Amelogenesis imperfecta is a hereditary malformation showing various manifestations regarding enamel dysplasia. This case report shows a 9-year follow-up after restorative treatment of a 16-year old female patient affected by a hypoplastic ...
Martin M. I. Sabandal +2 more
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Indian Journal of Dental Research, 2014 Amelogenesis imperfecta is a hereditary disorder with diverse clinical presentation, where enamel is the tissue that is primarily affected either quantitatively or qualitatively.
Veda Hegde, K Srikanth
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Prosthodontic rehabilitation of two siblings with hypoplastic (type 1) amelogenesis imperfecta: A case report [PDF]
HeliyonAmelogenesis imperfecta is a rare genetic disorder that interferes with normal enamel formation. Of the 4 main types of amelogenesis imperfecta, hypoplastic (type 1) is the most prevalent, characterized by a quantitative alteration in enamel. The pitting
Christina I. Wang, Naif Sinada
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Amelogenesis imperfecta in a family
Revista Cubana de Estomatología, 2018 Introduction: amelogenesis imperfecta consists of a group of hereditary disorders that affect the development of the dental enamel in such a way that the clinical appearance of all or almost all primary and permanent teeth is compromised.
Paula Hurtado-Villa +3 more
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Orthodontic management of amelogenesis imperfecta: A case report [PDF]
Clinical Case ReportsKey Clinical Message Amelogenesis imperfecta (AI) is a rare developmental anomaly characterized by poorly developed or absent tooth enamel, which complicates orthodontic treatment due to weak enamel‐bracket bond strength.
Kanistika Jha +3 more
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Unique Dental and Craniofacial Manifestations of Hypoplastic Amelogenesis Imperfecta in a Patient With Prune Belly Syndrome: A Rare Case Report [PDF]
Case Reports in DentistryConclusion: Although dental manifestations are not frequent in PBS, rare cases may present with aberrant hypoplastic amelogenesis imperfecta.
Jan Ching Chun Hu, Jung-Wook Kim
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