Antoniades K, Peonidis A, Pehlivanidis C, Kavadia S, Panagiotidis P
Department of Oral Surgery, Aristotle University of Thessaloniki, Greece.
Int J Oral Maxillofac Surg. 1994 Dec;23(6 Pt 1):363-5. doi: 10.1016/s0901-5027(05)80056-6.
The Smith-Lemli-Opitz syndrome is characterized by striking craniofacial features, microcephaly, mental deficiency, growth retardation, 2-3 syndactyly of the feet, and genital malformations. We present a patient and discuss dentofacial aspects of the syndrome.