Altuntas, ZeynepIsmayilzade, MajidAltuntas, MahmutYildirim, Mehmet E. C.2024-02-232024-02-2320201744-16251744-1633https://doi.org/10.1111/1744-1633.12459https://hdl.handle.net/20.500.12452/13756Van 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.eninfo:eu-repo/semantics/closedAccessCleft Lip And PalateVan Der Woude SyndromeVariable ExpressionArticle2441621642-s2.0-85092615242Q3WOS:00057916950000110.1111/1744-1633.12459