Congenital Cutis Laxa Associated with Growth Retardation

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dc.authoridEşrefoğlu, Mukaddes/0000-0003-3380-1480
dc.authorwosidOzcan, Hamdi/T-8408-2019
dc.authorwosidEşrefoğlu, Mukaddes/JWA-4590-2024
dc.contributor.authorSeyhan, M.
dc.contributor.authorEsrefoglu, M.
dc.contributor.authorOzcan, H.
dc.contributor.authorAkinci, A.
dc.date.accessioned2024-08-04T20:31:06Z
dc.date.available2024-08-04T20:31:06Z
dc.date.issued2008
dc.departmentİnönü Üniversitesien_US
dc.description.abstractCongenital cutis laxa is a rare, clinically and,genetically heterogeneous group of inherited disorders. It is characterized by degenerative changes in elastic fibres and manifests with skin laxity. Here we presented a six-month old boy with congenital cutis laxa associated with growth retardation. We reveal ultrastructural findings and discussed the differential diagnosis.en_US
dc.identifier.endpage409en_US
dc.identifier.issn0043-3144
dc.identifier.issn2309-5830
dc.identifier.issue4en_US
dc.identifier.pmid19566025en_US
dc.identifier.scopus2-s2.0-58149090872en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage406en_US
dc.identifier.urihttps://hdl.handle.net/11616/94720
dc.identifier.volume57en_US
dc.identifier.wosWOS:000262447900018en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherUniv West Indies Faculty Medical Sciencesen_US
dc.relation.ispartofWest Indian Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keywords]en_US
dc.titleCongenital Cutis Laxa Associated with Growth Retardationen_US
dc.typeArticleen_US

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