Noneruption of teeth in amelogenesis imperfecta: A report of two cases and review

Amelogenesis imperfecta (AI) comprises a complicated group of conditions, involving a structural defect of the tooth enamel, owing to certain genetic disturbances. It is expressed as an autosomal dominant, autosomal recessive or X-linked recessive trait. The structural pattern and clinical appearanc...

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Detalles Bibliográficos
Autores principales: Ray, Jaygopal G, Dutta, Sayani, Sarangi, Snehanjan, Yadav, Priyanka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364627/
https://www.ncbi.nlm.nih.gov/pubmed/35968177
http://dx.doi.org/10.4103/jomfp.JOMFP_471_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364627/
https://www.ncbi.nlm.nih.gov/pubmed/35968177
http://dx.doi.org/10.4103/jomfp.JOMFP_471_20

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