Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports

BACKGROUND: Hereditary enamel defect diseases are regrouped under the name “Amelogenesis Imperfecta” (AIH). Both dentitions are affected. Clinical expression is heterogeneous and varies between patients. Mutations responsible for this multigene disease may alter various genes and the inheritance can...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:BMC Oral Health
Main Authors: Toupenay, Steve, Fournier, Benjamin Philippe, Manière, Marie-Cécile, Ifi-Naulin, Chantal, Berdal, Ariane, de La Dure– Molla, Muriel
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2018
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6003150/
https://ncbi.nlm.nih.gov/pubmed/29907114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12903-018-0554-y
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