Monilethrix - Improvement with acitretin

Basit Öğe Kaydı
dc.contributor.authorKarincaoglu, Y
dc.contributor.authorCoskun, BK
dc.contributor.authorSeyhan, ME
dc.contributor.authorBayram, N
dc.date.accessioned2026-08-12T17:44:28Z
dc.date.issued2005
dc.departmentFırat Üniversitesi
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.
dc.identifier.doi10.2165/00128071-200506060-00008
dc.identifier.endpage410
dc.identifier.issn1175-0561
dc.identifier.issn1179-1888
dc.identifier.issue6
dc.identifier.pmid16343029
dc.identifier.scopus2-s2.0-31144464457
dc.identifier.scopusqualityQ1
dc.identifier.startpage407
dc.identifier.urihttps://doi.org/10.2165/00128071-200506060-00008
dc.identifier.urihttps://hdl.handle.net/11508/60277
dc.identifier.volume6
dc.identifier.wosWOS:000234608600007
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAdis Int Ltd
dc.relation.ispartofAmerican Journal of Clinical Dermatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectEtretinate Therapy
dc.subjectChildren
dc.subjectKeratinization
dc.subjectDisorders
dc.subjectRetinoids
dc.titleMonilethrix - Improvement with acitretin
dc.typeArticle

Dosyalar

Koleksiyon

WoS İndeksli Yayınlar Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu