Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.

@article{Cerqueira2008OrofacialMO,
  title={Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.},
  author={Daniella Ferraz Cerqueira and Ivete Pomarico Ribeiro de Souza},
  journal={Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics},
  year={2008},
  volume={105 3},
  pages={353-7}
}
Robinow's syndrome (Online Mendelian Inheritance in Man [OMIM] 268310), or fetal facies syndrome, is a rare genetic disorder causing autosomal dominant and recessive forms. This syndrome includes a series of anomalies such as short stature, characteristic facial dysmorphism (fetal facies), genital hypoplasia, and mesomelic brachymelia. The purpose of the present case is to describe the orofacial manifestations of the syndrome in a pediatric patient: craniofacial features, triangular mouth and a… CONTINUE READING
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