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Interdisciplinary Periodontal and Prosthetic Considerations in a Patient With Amelogenesis Imperfecta: A Case Report [PDF]

Clinical Case Reports
Amelogenesis imperfecta (AI) comprises a clinically and genetically heterogeneous group of conditions characterized by enamel hypoplasia and/or hypomineralization, which frequently complicate functional rehabilitation and restorative treatment planning ...
Kubra Burcu Yildirim, Gizem Ince Kuka, Hare Gursoy   +2 more
doaj   +3 more sources

Amelogenesis imperfecta [PDF]

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, Bloch-Zupan Agnes, Crawford Peter JM   +2 more
doaj   +3 more sources

Amelogenesis imperfecta. Case report [PDF]

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, Guido Alberto Perona-Miguel de Priego   +1 more
openaire   +4 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 Journal
Background: 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
doaj   +2 more sources

Timeline of Amelogenesis Imperfecta Management [PDF]

Journal of Craniofacial Surgery
Amelogenesis imperfecta is a heterogeneous group of >100 different rare diseases. Affected individuals and families are facing diagnostic uncertainty and wandering and a therapeutic odyssey. Continuous multidisciplinary management from childhood to adulthood is essential, emphasizing the critical role of health care professionals.
Jimenez-Armijo, Alexandra, Carvajal Monroy, Paola L, Ombashi, Saranda, Fennis, Willem M M, Ross, Jamila N, Van Den Boogaard, Marie-Jose H, Creton, Marijn A, Declerck, Dominique, Hermann, Xenia, Jung, Sophie, Berdal, Ariane, Fournier, Benjamin, Bugueno, Isaac Maximiliano, Ongkosuwito, Edwin, Bloch-Zupan, Agnès   +14 more
openaire   +6 more sources

Orthodontic management of amelogenesis imperfecta: A case report [PDF]

Clinical Case Reports
Key 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, Manoj Adhikari, Suraksha Shrestha, Anisha Pandey   +3 more
doaj   +2 more sources

Unique Dental and Craniofacial Manifestations of Hypoplastic Amelogenesis Imperfecta in a Patient With Prune Belly Syndrome: A Rare Case Report [PDF]

Case Reports in Dentistry
Conclusion: Although dental manifestations are not frequent in PBS, rare cases may present with aberrant hypoplastic amelogenesis imperfecta.
Jan Ching Chun Hu, Jung-Wook Kim
doaj   +2 more sources

Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta

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 ...
Figen Seymen, James Simmer
exaly   +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, S, McDonald, N, Arkutu, K, Malik   +3 more
openaire   +2 more sources

Management guidelines for amelogenesis imperfecta: a case report and review of the literature

Journal of Medical Case Reports, 2021
Background Rehabilitation of the entire dentition with amelogenesis imperfecta (AI) tends to pose a great challenge to the clinician. Most of the cases of amelogenesis imperfecta are reported to be associated with skeletal and dental deformities which ...
M. Roma, Puneet Hegde, M. Durga Nandhini, Shreya Hegde   +3 more
doaj   +1 more source