Ectodermal dysplasia - A rare case report

Ectodermal dysplasia (ED) is a rare genetic disease caused by developmental disturbances of embryonic ectoderm derived tissues, organs, and other accessory appendages. The congenital missing of teeth is usually bilateral. Anodontia or hypodontia may be associated with other ectodermal disturbances,...

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Detalles Bibliográficos
Autores principales: Bhakta, Poulomi, Barthunia, Bhavna, Nigam, Haritma, Pawar, Pallavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820434/
https://www.ncbi.nlm.nih.gov/pubmed/31681695
http://dx.doi.org/10.4103/jfmpc.jfmpc_625_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820434/
https://www.ncbi.nlm.nih.gov/pubmed/31681695
http://dx.doi.org/10.4103/jfmpc.jfmpc_625_19

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