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  • Title: Craniofacial manifestations of Smith-Lemli-Opitz syndrome: case report.
    Author: Antoniades K, Peonidis A, Pehlivanidis C, Kavadia S, Panagiotidis P.
    Journal: Int J Oral Maxillofac Surg; 1994 Dec; 23(6 Pt 1):363-5. PubMed ID: 7699276.
    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.
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