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Apert syndrome: a case report with discussion of craniofacial features
R P Paravatty1, A Ahsan, B T Sebastian
1Department of Oral Diagnosis, Medicine, and Radiology, College of Dental Surgery, Manipal, India. info@mahe.ernet.in
Quintessence International (Berlin, Germany : 1985)
|January 15, 2000
Abstract:
Apert syndrome is a rare congenital anomaly characterized by acrocephaly, syndactyly, and abnormalities of other organs. It has characteristic features in the orofacial region, affecting the eyes, palate, middle third of face, and uvula. In this case report, the features of Apert syndrome, particularly in relation to the orofacial region, are discussed.