SuicidDentistV1, Main, Exploration, bibRecord, 000297

Amelogenesis imperfecta: an introduction.

Identifieur interne : 000297 ( Main/Exploration ); précédent : 000296; suivant : 000298

Amelogenesis imperfecta: an introduction.

Auteurs : K. Gadhia [Niger] ; S. Mcdonald ; N. Arkutu ; K. Malik

Source :

British dental journal [ 1476-5373 ] ; 2012.

RBID : pubmed:22538897

Descripteurs français

KwdFr :
- Amélogenèse imparfaite (classification), Amélogenèse imparfaite (diagnostic), Amélogenèse imparfaite (génétique), Humains (MeSH), Phénotype (MeSH), Protéines de l'émail dentaire (génétique), Protéines de l'émail dentaire (métabolisme), Émail dentaire (physiopathologie).
MESH :
- diagnostic : Amélogenèse imparfaite.
- génétique : Amélogenèse imparfaite, Protéines de l'émail dentaire.
- métabolisme : Protéines de l'émail dentaire.
- physiopathologie : Émail dentaire.
- Humains, Phénotype.

English descriptors

KwdEn :
- Amelogenesis Imperfecta (classification), Amelogenesis Imperfecta (diagnosis), Amelogenesis Imperfecta (genetics), Dental Enamel (physiopathology), Dental Enamel Proteins (genetics), Dental Enamel Proteins (metabolism), Humans (MeSH), Phenotype (MeSH).
MESH :
- chemical , genetics : Dental Enamel Proteins.
- classification : Amelogenesis Imperfecta.
- diagnosis : Amelogenesis Imperfecta.
- genetics : Amelogenesis Imperfecta.
- chemical , metabolism : Dental Enamel Proteins.
- physiopathology : Dental Enamel.
- Humans, Phenotype.

Abstract

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. In this review paper, we look at the epidemiology, classification, aetiology, clinical description and diagnosis of AI. In the following three papers of this series, we aim to describe the role of paediatric dentists, orthodontists and restorative dentists in the clinical management of patients with AI.

DOI: 10.1038/sj.bdj.2012.314
PubMed: 22538897

Affiliations:

Niger

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Le document en format XML

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<front><div type="abstract" xml:lang="en">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. In this review paper, we look at the epidemiology, classification, aetiology, clinical description and diagnosis of AI. In the following three papers of this series, we aim to describe the role of paediatric dentists, orthodontists and restorative dentists in the clinical management of patients with AI.</div>
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Amelogenesis imperfecta: an introduction.

Amelogenesis imperfecta: an introduction.

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki