Variable expression of Van der Woude syndrome: A case report

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.

Source: Surgical Practice - October 19, 2020 Category: Surgery Authors: Zeynep Altunta ş, Majid Ismayilzade, Mahmut Altuntaş, Mehmet E. C. Yildirim Tags: CASE REPORT Source Type: research