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Ectodermal Dysplasia: A Case Report

Identifieur interne : 006A60 ( Ncbi/Checkpoint ); précédent : 006A59; suivant : 006A61

Ectodermal Dysplasia: A Case Report

Auteurs : Vinay K. Srivastava

Source :

RBID : PMC:5034093

Abstract

Ectodermal dysplasia is a hereditary disease characterized by dysplasia of tissues of ectodermal origin. The incidence of ectodermal dysplasia is rare (1 in 100,000 birth). This case report discusses the features, classification and prosthetic treatment plan (upper partial denture and lower complete denture for upper partial and lower complete edentulous arches respectively). This treatment plan would be able to provide psychological and functional boost to the sufferer.


Url:
DOI: 10.5005/jp-journals-10005-1124
PubMed: 27678241
PubMed Central: 5034093


Affiliations:


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PMC:5034093

Le document en format XML

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<p>Ectodermal dysplasia is a hereditary disease characterized by dysplasia of tissues of ectodermal origin. The incidence of ectodermal dysplasia is rare (1 in 100,000 birth). This case report discusses the features, classification and prosthetic treatment plan (upper partial denture and lower complete denture for upper partial and lower complete edentulous arches respectively). This treatment plan would be able to provide psychological and functional boost to the sufferer.</p>
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