Ectodermal Dysplasia: A Case Report
Identifieur interne : 006A60 ( Ncbi/Curation ); précédent : 006A59; suivant : 006A61Ectodermal Dysplasia: A Case Report
Auteurs : Vinay K. SrivastavaSource :
- International Journal of Clinical Pediatric Dentistry [ 0974-7052 ] ; 2011.
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.
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DOI: 10.5005/jp-journals-10005-1124
PubMed: 27678241
PubMed Central: 5034093
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<front><div type="abstract" xml:lang="en"><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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