1.
Int J Oral Maxillofac Surg
; 23(6 Pt 1): 363-5, 1994 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-7699276
RESUMO
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.