Hypohidrotic ectodermal dysplasia: Case reports

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dc.contributor.authorÖnçağ, Özant
dc.contributor.authorElbek, Çiğdem
dc.contributor.authorÖzkınay, Ferda
dc.date.accessioned2020-12-01T12:14:30Z
dc.date.available2020-12-01T12:14:30Z
dc.date.issued1999
dc.departmentEge Üniversitesien_US
dc.description.abstractHypohidrotic ectodermal dysplasia is a rare congenital syndrome which affects ectodermal structures. It is usually transmitted as an X-linked recessive trait. Rarely it can be transmitted autosomal recessively. Manifestations of this disorder may include teeth, skin, hair, nails and sweat glands. Most affected children require extensive dental treatment to restore their appearance and promote normal growth and development.en_US
dc.identifier.endpage48en_US
dc.identifier.issn1017-7698
dc.identifier.issue2en_US
dc.identifier.startpage45en_US
dc.identifier.urihttps://app.trdizin.gov.tr//makale/T0RFME1qST0
dc.identifier.urihttps://hdl.handle.net/11454/63893
dc.identifier.volume9en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofMedical Journal of Ege Universityen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectGenel ve Dahili Tıpen_US
dc.titleHypohidrotic ectodermal dysplasia: Case reportsen_US
dc.typeOtheren_US

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