Variable expression of Van der Woude syndrome: A case report
dc.contributor.author | Altuntas, Zeynep | |
dc.contributor.author | Ismayilzade, Majid | |
dc.contributor.author | Altuntas, Mahmut | |
dc.contributor.author | Yildirim, Mehmet E. C. | |
dc.date.accessioned | 2024-02-23T14:23:59Z | |
dc.date.available | 2024-02-23T14:23:59Z | |
dc.date.issued | 2020 | |
dc.department | NEÜ | en_US |
dc.description.abstract | Van 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.doi | 10.1111/1744-1633.12459 | |
dc.identifier.endpage | 164 | en_US |
dc.identifier.issn | 1744-1625 | |
dc.identifier.issn | 1744-1633 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.scopus | 2-s2.0-85092615242 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 162 | en_US |
dc.identifier.uri | https://doi.org/10.1111/1744-1633.12459 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12452/13756 | |
dc.identifier.volume | 24 | en_US |
dc.identifier.wos | WOS:000579169500001 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Surgical Practice | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Cleft Lip And Palate | en_US |
dc.subject | Van Der Woude Syndrome | en_US |
dc.subject | Variable Expression | en_US |
dc.title | Variable expression of Van der Woude syndrome: A case report | en_US |
dc.type | Article | en_US |