Lamellar ichthyosis: a case report

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dc.contributor.authorÖzyürek, Hamit
dc.contributor.authorKavak, Ayşe
dc.contributor.authorAlper, Murat
dc.date.accessioned2020-04-30T23:18:50Z
dc.date.available2020-04-30T23:18:50Z
dc.date.issued2002
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.descriptionalper, murat/0000-0001-7069-0623; kavak, ayse/0000-0002-4679-1181en_US
dc.descriptionWOS: 000173860500013en_US
dc.descriptionPubMed: 11858382en_US
dc.description.abstractIchthyoses are divided into four groups according to clinical, histopathologic and genetic findings. Lamellar ichthyosis is one of them. The incidence of lamellar ichthyosis is believed to be approximately 1 per 100,000 to 300,000 live births. It is characterized by large, polygonal, grayish brown, and tightly adherent scales. We report a four-year-old boy with desquamative lesions since birth who had six-year-old sister with similar lesions, suggesting an autosomal recessive inheritance. His skin biopsy revealed hyperkeratosis with lamellae. There were no associated hair or neurological abnormalities. His clinical and histopathological findings were typical for isolated lamellar ichthyosis. Because of its rare occurrence, we report this case with a review of the literature.en_US
dc.identifier.endpage60en_US
dc.identifier.issn0041-4301
dc.identifier.issue1en_US
dc.identifier.startpage58en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12684/3547
dc.identifier.volume44en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherTurkish J Pediatricsen_US
dc.relation.ispartofTurkish Journal Of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectlamellar ichthyosisen_US
dc.subjecttreatmenten_US
dc.subjectectropionen_US
dc.titleLamellar ichthyosis: a case reporten_US
dc.typeArticleen_US

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