Van der Woude Syndrome (VWS) is a rare genetic disorder that primarily affects the development of the orofacial region. Although it is relatively uncommon, with an estimated prevalence of approximately 1 in 35,000 to 1 in 100,000 live births, its impact on affected individuals can be significant, especially in terms of speech, feeding, and dental development. However, not all individuals with VWS present with all these features, and the severity of symptoms can vary greatly.