HED (Hypohidrotic Ectodermal Dysplasia): A Review

dc.contributor.authorCallea M.
dc.contributor.authorScalisi F.C.
dc.contributor.authorYavuz I.
dc.contributor.authorDogan M.S.
dc.contributor.authorWilloughby C.E.
dc.contributor.authorBashyam M.D.
dc.date.accessioned2024-04-24T18:46:39Z
dc.date.available2024-04-24T18:46:39Z
dc.date.issued2021
dc.departmentDicle Üniversitesien_US
dc.description.abstractAbstract The ectodermal dysplasias (EDs) are a heterogeneous group of inherited, developmental disorders characterized by alterations in two or more ectodermal structures including the hair, teeth, nails and sweat glands. Currently, more than 200 types of ectodermal dysplasias have been described. Anhidrotic or hypohidrotic ectodermal dysplasia (AED/HED), the most common ED, is characterized by three cardinal features: hypotrichosis, hypohidrosis and hypodontia. We review the genetic and pathogenetic mechanisms of AED/HED and report on the management of clinical manifestations driven by embryology, anatomy and physiology. © 2021, Journal of International Dental and Medical Research, All Rights Reserved.en_US
dc.identifier.endpage789en_US
dc.identifier.issn1309-100X
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-85110678843
dc.identifier.scopusqualityQ3
dc.identifier.startpage785en_US
dc.identifier.urihttps://hdl.handle.net/11468/25276
dc.identifier.volume14en_US
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherUniversity of Dicleen_US
dc.relation.ispartofJournal of International Dental and Medical Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnhidrotic Or Hypohidrotic Ectodermal Dysplasiaen_US
dc.subjectClinicalen_US
dc.subjectEctodermal Dysplasiasen_US
dc.subjectEthiopathogenesisen_US
dc.titleHED (Hypohidrotic Ectodermal Dysplasia): A Reviewen_US
dc.titleHED (Hypohidrotic Ectodermal Dysplasia): A Review
dc.typeArticleen_US

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