Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary disease · Multiple congenital anomalies/dysmorphic syndrome without intellectual disability · IRF6-related condition
Van der Woude syndrome
Van der Woude syndrome (VWS) is a rare congenital genetic dysmorphic syndrome characterized by paramedian lower-lip fistulae, cleft lip with or without cleft palate, or isolated cleft palate.
-
Van der Woude syndrome 1 0 trials
-
Van der Woude syndrome 2 0 trials