Monilethrix - Improvement with acitretin

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dc.contributor.authorKarincaoglu, Y
dc.contributor.authorCoskun, BK
dc.contributor.authorSeyhan, ME
dc.contributor.authorBayram, N
dc.date.accessioned2024-08-04T20:15:12Z
dc.date.available2024-08-04T20:15:12Z
dc.date.issued2005
dc.departmentİnönü Üniversitesien_US
dc.description.abstractMonilethrix is a rare hereditary disorder that affects the hair and is characterized by shaft anomaly. There is no known treatment that successfully cures the condition. In this report we present a case of monilethrix in a 7-year-old girl treated with oral acitretin. A very good clinical and cosmetic result was obtained while treatment was continued. However, clinical symptoms recurred after discontinuation of acitretin therapy.en_US
dc.identifier.doi10.2165/00128071-200506060-00008
dc.identifier.endpage410en_US
dc.identifier.issn1175-0561
dc.identifier.issn1179-1888
dc.identifier.issue6en_US
dc.identifier.pmid16343029en_US
dc.identifier.scopus2-s2.0-31144464457en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage407en_US
dc.identifier.urihttps://doi.org/10.2165/00128071-200506060-00008
dc.identifier.urihttps://hdl.handle.net/11616/94240
dc.identifier.volume6en_US
dc.identifier.wosWOS:000234608600007en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherAdis Int Ltden_US
dc.relation.ispartofAmerican Journal of Clinical Dermatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEtretinate Therapyen_US
dc.subjectChildrenen_US
dc.subjectKeratinizationen_US
dc.subjectDisordersen_US
dc.subjectRetinoidsen_US
dc.titleMonilethrix - Improvement with acitretinen_US
dc.typeArticleen_US

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