Hypohidrotic ectodermal dysplasia: A case report
dc.contributor.author | Yavuz, Izzet | |
dc.contributor.author | Kiralp, Suha | |
dc.contributor.author | Baskan, Zelal | |
dc.date.accessioned | 2024-04-24T17:37:30Z | |
dc.date.available | 2024-04-24T17:37:30Z | |
dc.date.issued | 2008 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Ectodermal dysplasias represent a large and complex group of diseases comprising more than 170 clinical conditions. They are caused by impaired development of the ectodermal appendages and characterized by a primary defect in at least one of the following tissues: nails, hair, sweat glands, or teeth. Ectodermal dysplasia has emotional consequences for affected individuals at early ages. This case report outlines a possible routine approach to restoring function and esthetics and aiding in the social interaction for a 9-year-old girl diagnosed with hypohidrotic ectodermal dysplasia at about 7 years of age. | en_US |
dc.identifier.endpage | 86 | en_US |
dc.identifier.issn | 0033-6572 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 18551221 | |
dc.identifier.scopus | 2-s2.0-37349031797 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 81 | en_US |
dc.identifier.uri | https://hdl.handle.net/11468/20973 | |
dc.identifier.volume | 39 | en_US |
dc.identifier.wos | WOS:000253442700012 | |
dc.identifier.wosquality | Q4 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | en_US |
dc.publisher | Quintessence Publishing Co Inc | en_US |
dc.relation.ispartof | Quintessence International | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Ectodermal Dysplasia | en_US |
dc.subject | Fixed Prosthesis | en_US |
dc.subject | Hypodontia | en_US |
dc.title | Hypohidrotic ectodermal dysplasia: A case report | en_US |
dc.title | Hypohidrotic ectodermal dysplasia: A case report | |
dc.type | Article | en_US |