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Craniofacial manifestations of Smith-Lemli-Opitz syndrome: case report
K Antoniades1, A Peonidis, C Pehlivanidis
1Department of Oral Surgery, Aristotle University of Thessaloniki, Greece.
International Journal of Oral and Maxillofacial Surgery
|December 1, 1994
Abstract:
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.