Amélogenèse imparfaite héréditaire et béance antérieure : comment optimiser la prise en charge ? Une revue de la littérature (notice n° 767979)
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| fixed length control field | 03345cam a2200337 4500500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250123104639.0 |
| 041 ## - LANGUAGE CODE | |
| Language code of text/sound track or separate title | fre |
| 042 ## - AUTHENTICATION CODE | |
| Authentication code | dc |
| 100 10 - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Foumou-Moretti, Nathalie |
| Relator term | author |
| 245 00 - TITLE STATEMENT | |
| Title | Amélogenèse imparfaite héréditaire et béance antérieure : comment optimiser la prise en charge ? Une revue de la littérature |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Date of publication, distribution, etc. | 2021.<br/> |
| 500 ## - GENERAL NOTE | |
| General note | 95 |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Introduction : L’amélogenèse imparfaite est une pathologie d’origine génétique qui se caractérise par une anomalie de structure de l’émail et possède une expression clinique variable. Elle peut être isolée ou survenir dans le cadre d’un syndrome. Trois formes cliniques existent : hypoplasique, hypomature et hypominéralisée. Discussion : Si la fragilité amélaire à l’origine d’une exposition de la dentine et d’une hypersensibilité dentaire sont des conséquences fréquentes de la maladie, certaines formes sévères sont surtout associées à une béance antérieure. La prise en charge de ces patients constitue alors un réel défi pour le chirurgien-dentiste. Matériels et méthodes : Une revue de la littérature a été effectuée à l’aide des interfaces PubMed, Web of Science et Scopus sur les dix dernières années afin de mettre en évidence les différentes thérapeutiques envisageables. Conclusion : Du traitement conservateur à la prise en charge chirurgicale, il est nécessaire de mettre en place une collaboration entre l’orthodontiste et l’odontologiste pédiatrique afin de proposer une prise en charge multidisciplinaire adaptée aux besoins du patient. |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Introduction: Amelogenesis imperfecta is a genetic disease, characterized by a structural defect of the enamel and has variable clinical expressions. It can be isolated or associated as part of a syndrome. Three clinical forms exist: hypoplastic, hypomature and hypomineralized. Discussion: Enamel fragility involves dentin exposure and dental hypersensitivity as frequent consequences. Some severe forms are mainly associated with an anterior open bite. The care of these patients constitutes a real challenge for the dentist. Materials et Methods: A literature review was carried out using the PubMed, Web of Science and Scopus interfaces over the past ten years in order to highlight the different treatment options available. Conclusion: From conservative to surgical treatment, it is necessary to develop a collaboration between the orthodontist and the pediatric dentist in order to offer multidisciplinary care adapted to the patient's needs. |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Maladies génétiques congénitales |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Béance dentaire |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Amélogenèse imparfaite |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Malformations dentaires |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Revue de la littérature |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Review of the literature |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Genetic diseases inborn |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Amelogenesis imperfecta |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Tooth abnormalities |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Open bite |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Trentesaux, Thomas |
| Relator term | author |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Bocquet, Emmanuelle |
| Relator term | author |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Delfosse, Caroline |
| Relator term | author |
| 700 10 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Marquillier, Thomas |
| Relator term | author |
| 786 0# - DATA SOURCE ENTRY | |
| Note | L'Orthodontie Française | 92 | 4 | 2021-10-01 | p. 421-430 | 1966-5202 |
| 856 41 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://shs.cairn.info/revue-l-orthodontie-francaise-2021-4-page-421?lang=fr&redirect-ssocas=7080">https://shs.cairn.info/revue-l-orthodontie-francaise-2021-4-page-421?lang=fr&redirect-ssocas=7080</a> |
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