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J Craniofac Surg ; 31(6): e574-e577, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32569048

RESUMO

Roberts Syndrome is an extremely rare syndrome reporting about 150 cases in the literature, with a very low survival rate. The authors present a case of a female patient with Roberts Syndrome who also had a coronal craniosynostosis. The aim of this case report is to present a case of a patient with Roberts Syndrome with a brachycephaly that required management of fronto-orbital advancement. In conclusion Roberts Syndrome is a rare disease, which can have different skeletal variations. This syndrome can manifest itself with craniosynostosis, with the requirement of a comprehensive management to correct it and avoid compression of the brain with endocranial hypertension.


Assuntos
Anormalidades Craniofaciais/cirurgia , Ectromelia/cirurgia , Osso Frontal/cirurgia , Hipertelorismo/cirurgia , Órbita/cirurgia , Craniossinostoses/cirurgia , Feminino , Humanos , Lactente , Procedimentos de Cirurgia Plástica
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