Variable expression of Van der Woude syndrome: A case report

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dc.contributor.authorAltuntas, Zeynep
dc.contributor.authorIsmayilzade, Majid
dc.contributor.authorAltuntas, Mahmut
dc.contributor.authorYildirim, Mehmet E. C.
dc.date.accessioned2024-02-23T14:23:59Z
dc.date.available2024-02-23T14:23:59Z
dc.date.issued2020
dc.departmentNEÜen_US
dc.description.abstractVan der Woude syndrome (VWS) is an autosomal dominant disorder with a rare clinical manifestation of orofacial disorders with deletion in the 1q32-q41 chromosome band. In our study we present a clinical case of a 1-year old boy with a bilateral cleft lip, a cleft palate and bilateral congenital pits on the lower lip and a father with various clinical presentations of VWS.en_US
dc.identifier.doi10.1111/1744-1633.12459
dc.identifier.endpage164en_US
dc.identifier.issn1744-1625
dc.identifier.issn1744-1633
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-85092615242en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage162en_US
dc.identifier.urihttps://doi.org/10.1111/1744-1633.12459
dc.identifier.urihttps://hdl.handle.net/20.500.12452/13756
dc.identifier.volume24en_US
dc.identifier.wosWOS:000579169500001en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofSurgical Practiceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCleft Lip And Palateen_US
dc.subjectVan Der Woude Syndromeen_US
dc.subjectVariable Expressionen_US
dc.titleVariable expression of Van der Woude syndrome: A case reporten_US
dc.typeArticleen_US

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