Apert syndrome: A case report with discussion of craniofacial features

Apert syndrome is a rare congenital anomaly characterized by acrocephaly, s yndactyly, and abnormalities of other organs. It has characteristic feature s in the orofacial region, affecting the eyes, palate, middle third of face , and uvula. In this case report, the features of Apert syndrome, particula rly in relation to the orofacial region, are discussed.