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

Abstract

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 long upper lip philtrum, ankyloglossia, a shortened tongue devoid of tongue tip, a geographic tongue, arched palate, gingival hyperplasia, dental abnormalities (misaligned and crowded teeth), and delayed tooth eruption.

Authors+Show Affiliations

Department of Pediatric Dentistry and Orthodontics, School of Dentistry, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.No affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

18061493

Citation

Cerqueira, Daniella Ferraz, and Ivete Pomarico Ribeiro de Souza. "Orofacial Manifestations of Robinow's Syndrome: a Case Report in a Pediatric Patient." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, vol. 105, no. 3, 2008, pp. 353-7.
Cerqueira DF, de Souza IP. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105(3):353-7.
Cerqueira, D. F., & de Souza, I. P. (2008). Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 105(3), 353-7.
Cerqueira DF, de Souza IP. Orofacial Manifestations of Robinow's Syndrome: a Case Report in a Pediatric Patient. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008;105(3):353-7. PubMed PMID: 18061493.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient. AU - Cerqueira,Daniella Ferraz, AU - de Souza,Ivete Pomarico Ribeiro, Y1 - 2007/12/03/ PY - 2006/01/27/received PY - 2007/05/23/revised PY - 2007/05/28/accepted PY - 2007/12/7/pubmed PY - 2008/4/9/medline PY - 2007/12/7/entrez SP - 353 EP - 7 JF - Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics JO - Oral Surg Oral Med Oral Pathol Oral Radiol Endod VL - 105 IS - 3 N2 - 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 long upper lip philtrum, ankyloglossia, a shortened tongue devoid of tongue tip, a geographic tongue, arched palate, gingival hyperplasia, dental abnormalities (misaligned and crowded teeth), and delayed tooth eruption. SN - 1528-395X UR - https://www.unboundmedicine.com/medline/citation/18061493/Orofacial_manifestations_of_Robinow's_syndrome:_a_case_report_in_a_pediatric_patient_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S1079-2104(07)00470-2 DB - PRIME DP - Unbound Medicine ER -